sample_sheet <- glue::glue("sample_sheets/tmrc2_samples_20210817.xlsx")

1 Introduction

This document is intended to provide a general overview of the TMRC2 samples which have thus far been sequenced. In some cases, this includes only those samples starting in 2019; in other instances I am including our previous (2015-2016) samples.

In all cases the processing performed was:

Default trimming was performed.
Hisat2 was used to map the remaining reads against the Leishmania panamensis genome revision 36.
The alignments from hisat2 were used to count reads/gene against the revision 36 annotations with htseq.
These alignments were also passed to the pileup functionality of samtools and the vcf/bcf utilities in order to make a matrix of all observed differences between each sample with respect to the reference.

The analyses in this document use the matrices of counts/gene from #3 and variants/position from #4 in order to provide some images and metrics describing the samples we have sequenced so far.

2 Annotations

Everything which follows depends on the Existing TriTrypDB annotations revision 46, circa 2019. The following block loads a database of these annotations and turns it into a matrix where the rows are genes and columns are all the annotation types provided by TriTrypDB.

The same database was used to create a matrix of orthologous genes between L.panamensis and all of the other species in the TriTrypDB.

tt <- sm(library(EuPathDB))
tt <- sm(library(org.Lpanamensis.MHOMCOL81L13.v46.eg.db))
pan_db <- org.Lpanamensis.MHOMCOL81L13.v46.eg.db
all_fields <- columns(pan_db)

all_lp_annot <- sm(load_orgdb_annotations(
    pan_db,
    keytype = "gid",
    fields = c("annot_gene_entrez_id", "annot_gene_name",
               "annot_strand", "annot_chromosome", "annot_cds_length",
               "annot_gene_product")))$genes

lp_go <- sm(load_orgdb_go(pan_db))
lp_lengths <- all_lp_annot[, c("gid", "annot_cds_length")]
colnames(lp_lengths)  <- c("ID", "length")
all_lp_annot[["annot_gene_product"]] <- tolower(all_lp_annot[["annot_gene_product"]])
orthos <- sm(EuPathDB::extract_eupath_orthologs(db = pan_db))

hisat_annot <- all_lp_annot
## rownames(hisat_annot) <- paste0("exon_", rownames(hisat_annot), ".E1")

3 Load a genome

meta <- EuPathDB::download_eupath_metadata(webservice="tritrypdb")

## Appending to an existing file: EuPathDB/metadata/biocv3.13_tritrypdbv53_metadata.csv

## Appending to an existing file: EuPathDB/metadata/GRanges_biocv3.13_tritrypdbv53_metadata.csv

## Appending to an existing file: EuPathDB/metadata/OrgDb_biocv3.13_tritrypdbv53_metadata.csv

## Appending to an existing file: EuPathDB/metadata/TxDb_biocv3.13_tritrypdbv53_metadata.csv

## Appending to an existing file: EuPathDB/metadata/OrganismDbi_biocv3.13_tritrypdbv53_metadata.csv

## Appending to an existing file: EuPathDB/metadata/BSgenome_biocv3.13_tritrypdbv53_metadata.csv

## Appending to an existing file: EuPathDB/metadata/biocv3.13_tritrypdbv53_invalid_metadata.csv

## Appending to an existing file: EuPathDB/metadata/GRanges_biocv3.13_tritrypdbv53_invalid_metadata.csv

## Appending to an existing file: EuPathDB/metadata/OrgDb_biocv3.13_tritrypdbv53_invalid_metadata.csv

## Appending to an existing file: EuPathDB/metadata/TxDb_biocv3.13_tritrypdbv53_invalid_metadata.csv

## Appending to an existing file: EuPathDB/metadata/OrganismDbi_biocv3.13_tritrypdbv53_invalid_metadata.csv

## Appending to an existing file: EuPathDB/metadata/BSgenome_biocv3.13_tritrypdbv53_invalid_metadata.csv

lp_entry <- EuPathDB::get_eupath_entry(species="Leishmania panamensis", metadata=meta)

## Found the following hits: Leishmania panamensis MHOM/COL/81/L13, Leishmania panamensis strain MHOM/PA/94/PSC-1, choosing the first.

## Using: Leishmania panamensis MHOM/COL/81/L13.

lp_entry

##   AnnotationVersion AnnotationSource BiocVersion DataProvider
## 6      Dec 16, 2014           GeneDB        3.13    TriTrypDB
##                                 Genome GenomeSource   GenomeVersion
## 6 TriTrypDB-53_LpanamensisMHOMCOL81L13      GenBank GCA_000340495.1
##   NumArrayGene NumChipChipGene NumChromosome NumCodingGene NumCommunity
## 6         <NA>            <NA>            36          8665           12
##   NumContig NumEC NumEST NumGene NumGO NumOrtholog NumOtherGene NumPopSet
## 6         0    62   <NA>    8778  3930        8665          113     37300
##   NumProteomics NumPseudogene NumRNASeq NumRTPCR NumSNP NumTFBS Organellar
## 6          <NA>             0      <NA>       NA   5337      NA         no
##   ReferenceStrain   MegaBP                            PrimaryKey ProjectID
## 6             yes    31.26 Leishmania panamensis MHOM/COL/81/L13 TriTrypDB
##                             RecordClassName          SourceID SourceVersion
## 6 OrganismRecordClasses.OrganismRecordClass NCBITAXON_1055687            53
##   TaxonomyID                          TaxonomyName
## 6    1295824 Leishmania panamensis MHOM/COL/81/L13
##                                                                                                                               URLGenome
## 6 http://TriTrypDB.org/common/downloads/release-53/LpanamensisMHOMCOL81L13/fasta/data/TriTrypDB-53_LpanamensisMHOMCOL81L13_Genome.fasta
##                                                                                                                       URLGFF
## 6 http://TriTrypDB.org/common/downloads/release-53/LpanamensisMHOMCOL81L13/gff/data/TriTrypDB-53_LpanamensisMHOMCOL81L13.gff
##                                                                                                                                         URLProtein
## 6 http://TriTrypDB.org/common/downloads/release-53/LpanamensisMHOMCOL81L13/fasta/data/TriTrypDB-53_LpanamensisMHOMCOL81L13_AnnotatedProteins.fasta
##   Coordinate_1_based                       Maintainer
## 6               TRUE Keith Hughitt <khughitt@umd.edu>
##                                                                                                                    SourceUrl
## 6 http://TriTrypDB.org/common/downloads/release-53/LpanamensisMHOMCOL81L13/gff/data/TriTrypDB-53_LpanamensisMHOMCOL81L13.gff
##                                                                                   Tags
## 6 Annotation:EuPathDB:Eukaryote:Pathogen:Parasite:Trypanosome:Kinetoplastid:Leishmania
##                                       BsgenomePkg
## 6 BSGenome.Leishmania.panamensis.MHOMCOL81L13.v53
##                                           GrangesPkg
## 6 GRanges.Leishmania.panamensis.MHOMCOL81L13.v53.rda
##                                     OrganismdbiPkg
## 6 tritrypdb.Leishmania.panamensis.MHOMCOL81L13.v53
##                                 OrgdbPkg
## 6 org.Lpanamensis.MHOMCOL81L13.v53.eg.db
##                                                 TxdbPkg
## 6 TxDb.Leishmania.panamensis.MHOMCOL81L13.TriTrypDB.v53
##                                Taxon      Genus    Species       Strain
## 6 Leishmania panamensis MHOMCOL81L13 Leishmania panamensis MHOMCOL81L13
##                                                                                   BsgenomeFile
## 6 EuPathDB/BSgenome/3.13/BSGenome.Leishmania.panamensis.MHOMCOL81L13.v53/single_sequences.2bit
##                                                                GrangesFile
## 6 EuPathDB/GRanges/3.13/GRanges.Leishmania.panamensis.MHOMCOL81L13.v53.rda
##                                                                            OrganismdbiFile
## 6 EuPathDB/OrganismDbi/3.13/tritrypdb.Leishmania.panamensis.MHOMCOL81L13.v53/graphInfo.rda
##                                                        OrgdbFile
## 6 EuPathDB/OrgDb/3.13/org.Lpanamensis.MHOMCOL81L13.v53.eg.sqlite
##                                                                          TxdbFile
## 6 EuPathDB/TxDb/3.13/TxDb.Leishmania.panamensis.MHOMCOL81L13.TriTrypDB.v53.sqlite
##            GenusSpecies                       TaxonUnmodified
## 6 Leishmania panamensis Leishmania panamensis MHOM/COL/81/L13
##                          TaxonCanonical                             TaxonXref
## 6 Leishmania panamensis MHOM/COL/81/L13 Leishmania panamensis MHOM/COL/81/L13

## testing_panamensis <- EuPathDB::make_eupath_bsgenome(entry=lp_entry)
library(as.character(testing_panamensis), character.only=TRUE)

## Error in library(as.character(testing_panamensis), character.only = TRUE): object 'testing_panamensis' not found

genome <- get0(as.character(testing_panamensis))

## Error in get0(as.character(testing_panamensis)): object 'testing_panamensis' not found

4 TODO:

Resequence samples: TMRC20002, TMRC20006, TMRC20004 (maybe TMRC20008 and TMRC20029)

5 Generate Expressionsets and Sample Estimation

The process of sample estimation takes two primary inputs:

The sample sheet, which contains all the metadata we currently have on hand, including filenames for the outputs of #3 and #4 above.
The gene annotations.

An expressionset is a data structure used in R to examine RNASeq data. It is comprised of annotations, metadata, and expression data. In the case of our processing pipeline, the location of the expression data is provided by the filenames in the metadata.

The first lines of the following block create the Expressionset. All of the following lines perform various normalizations and generate plots from it.

5.1 Notes

The following samples are much lower coverage:

TMRC20002
TMRC20006
TMRC20007
TMRC20008

20210610: I made some manual changes to the sample sheet which I downloaded, filling in some zymodeme with ‘unknown’

5.2 TODO:

Do the multi-gene family removal right here instead of way down at the bottom
Add zymodeme snps to the annotation later.
Start phylogenetic analysis of variant table.

sanitize_columns <- c("passagenumber", "clinicalresponse", "clinicalcategorical",
                      "zymodemecategorical", "phenotypiccharacteristics")
lp_expt <- sm(create_expt(sample_sheet,
                          gene_info = hisat_annot,
                          id_column = "hpglidentifier",
                          file_column = "lpanamensisv36hisatfile")) %>%
  set_expt_conditions(fact = "zymodemecategorical") %>%
  subset_expt(nonzero = 8550) %>%
  subset_expt(coverage = 5000000) %>%
  semantic_expt_filter(semantic = c("amastin", "gp63", "leishmanolysin"),
                       semantic_column = "annot_gene_product") %>%
  sanitize_expt_metadata(columns = sanitize_columns) %>%
  set_expt_factors(columns = sanitize_columns, class = "factor")

## The samples (and read coverage) removed when filtering 8550 non-zero genes are:

## TMRC20002 TMRC20006 
##  11681227   6670348

## subset_expt(): There were 74, now there are 72 samples.

## The samples removed (and read coverage) when filtering samples with less than 5e+06 reads are:

## TMRC20004 TMRC20029 
##    564812   1658096

## subset_expt(): There were 72, now there are 70 samples.

## semantic_expt_filter(): Removed 68 genes.

libsizes <- plot_libsize(lp_expt)
pp(file = "images/lp_expt_libsizes.png", image = libsizes$plot, width = 14, height = 9)

## I think samples 7,10 should be removed at minimum, probably also 9,11
nonzero <- plot_nonzero(lp_expt)
pp(file = "images/lp_nonzero.png", image = nonzero$plot, width = 9, height = 9)

## Warning: ggrepel: 49 unlabeled data points (too many overlaps). Consider
## increasing max.overlaps

## Warning: ggrepel: 53 unlabeled data points (too many overlaps). Consider
## increasing max.overlaps

lp_box <- plot_boxplot(lp_expt)

## 5252 entries are 0.  We are on a log scale, adding 1 to the data.

pp(file = "images/lp_expt_boxplot.png", image = lp_box, width = 12, height = 9)

filter_plot <- plot_libsize_prepost(lp_expt)
filter_plot$lowgene_plot

## Warning: Using alpha for a discrete variable is not advised.

filter_plot$count_plot

5.3 Distribution Visualization

Najib’s favorite plots are of course the PCA/TNSE. These are nice to look at in order to get a sense of the relationships between samples. They also provide a good opportunity to see what happens when one applies different normalizations, surrogate analyses, filters, etc. In addition, one may set different experimental factors as the primary ‘condition’ (usually the color of plots) and surrogate ‘batches’.

5.4 By Susceptilibity

Column ‘Q’ in the sample sheet, make a categorical version of it with these parameters:

0 <= x <= 35 is resistant
36 <= x <= 48 is ambiguous
49 <= x is sensitive

starting <- as.numeric(pData(lp_expt)[["susceptibilityinfectionreduction32ugmlsbvhistoricaldata"]])
sus_categorical <- starting
na_idx <- is.na(starting)
sus_categorical[na_idx] <- "unknown"

resist_idx <- starting <= 0.35
sus_categorical[resist_idx] <- "resistant"
indeterminant_idx <- starting >= 0.36 & starting <= 0.48
sus_categorical[indeterminant_idx] <- "ambiguous"
susceptible_idx <- starting >= 0.49
sus_categorical[susceptible_idx] <- "sensitive"

pData(lp_expt$expressionset)[["sus_category"]] <- sus_categorical

clinical_colors <- list(
    "z2.3" = "#874400",
    "z2.2" = "#df7000",
    "unknown" = "#cbcbcb",
    "null" = "#000000")
clinical_samples <- lp_expt %>%
  set_expt_batches(fact = sus_categorical) %>%
  set_expt_colors(clinical_colors)

clinical_norm <- sm(normalize_expt(clinical_samples, norm = "quant", transform = "log2",
                                   convert = "cpm", batch = FALSE, filter = TRUE))
zymo_pca <- plot_pca(clinical_norm, plot_title = "PCA of parasite expression values",
                     plot_labels = FALSE)
pp(file = "images/zymo_pca_sus_shape.png", image = zymo_pca$plot)

zymo_3dpca <- plot_3d_pca(zymo_pca)
zymo_3dpca$plot

clinical_n <- sm(normalize_expt(clinical_samples, transform = "log2",
                                convert = "cpm", batch = FALSE, filter = TRUE))
zymo_tsne <- plot_tsne(clinical_n, plot_title = "TSNE of parasite expression values")
zymo_tsne$plot

## Warning: ggrepel: 8 unlabeled data points (too many overlaps). Consider
## increasing max.overlaps

clinical_nb <- normalize_expt(clinical_samples, convert = "cpm", transform = "log2",
                         filter = TRUE, batch = "svaseq")

## Removing 142 low-count genes (8568 remaining).

## batch_counts: Before batch/surrogate estimation, 989 entries are x==0: 0%.

## batch_counts: Before batch/surrogate estimation, 3326 entries are 0<x<1: 1%.

## Setting 335 low elements to zero.

## transform_counts: Found 335 values equal to 0, adding 1 to the matrix.

clinical_nb_pca <- plot_pca(clinical_nb, plot_title = "PCA of parasite expression values",
                            plot_labels = FALSE)
pp(file = "images/clinical_nb_pca_sus_shape.png", image = clinical_nb_pca$plot)

clinical_nb_tsne <- plot_tsne(clinical_nb, plot_title = "TSNE of parasite expression values")
clinical_nb_tsne$plot

## Warning in MASS::cov.trob(data[, vars]): Probable convergence failure

## Warning in MASS::cov.trob(data[, vars]): Probable convergence failure

## Warning: ggrepel: 70 unlabeled data points (too many overlaps). Consider
## increasing max.overlaps

corheat <- plot_corheat(clinical_norm, plot_title = "Correlation heatmap of parasite
                 expression values
")
corheat$plot

plot_sm(clinical_norm)$plot

## Performing correlation.

5.5 By Cure/Fail status

cf_colors <- list(
    "cure" = "#006f00",
    "fail" = "#9dffa0",
    "unknown" = "#cbcbcb",
    "notapplicable" = "#000000")
cf_expt <- set_expt_conditions(lp_expt, fact = "clinicalcategorical") %>%
  set_expt_batches(fact = sus_categorical) %>%
  set_expt_colors(cf_colors)

cf_norm <- normalize_expt(cf_expt, convert = "cpm", transform = "log2",
                          norm = "quant", filter = TRUE)

## Removing 142 low-count genes (8568 remaining).

## transform_counts: Found 2 values equal to 0, adding 1 to the matrix.

start_cf <- plot_pca(cf_norm, plot_title = "PCA of parasite expression values",
                     plot_labels = FALSE)
pp(file = "images/cf_sus_shape.png", image = start_cf$plot)

cf_nb <- normalize_expt(cf_expt, convert = "cpm", transform = "log2",
                        norm = "quant", filter = TRUE, batch = "svaseq")

## Warning in normalize_expt(cf_expt, convert = "cpm", transform = "log2", :
## Quantile normalization and sva do not always play well together.

## Removing 142 low-count genes (8568 remaining).

## batch_counts: Before batch/surrogate estimation, 2 entries are x==0: 0%.

## batch_counts: Before batch/surrogate estimation, 4074 entries are 0<x<1: 1%.

## Setting 181 low elements to zero.

## transform_counts: Found 181 values equal to 0, adding 1 to the matrix.

cf_nb_pca <- plot_pca(cf_nb, plot_title = "PCA of parasite expression values",
                      plot_labels = FALSE)
pp(file = "images/cf_sus_share_nb.png", image = cf_nb_pca$plot)

cf_norm <- normalize_expt(cf_expt, transform = "log2", convert = "cpm",
                          filter = TRUE, norm = "quant")

## Removing 142 low-count genes (8568 remaining).

## transform_counts: Found 2 values equal to 0, adding 1 to the matrix.

test <- pca_information(cf_norm,
                        expt_factors = c("clinicalcategorical", "zymodemecategorical",
                                         "pathogenstrain", "passagenumber"),
                        num_components = 6, plot_pcas = TRUE)
test$anova_p

##                           PC1       PC2    PC3       PC4     PC5       PC6
## clinicalcategorical 0.2746798 0.0762058 0.3880 2.535e-04 0.34372 8.192e-01
## zymodemecategorical 0.0004562 0.8405440 0.4855 1.353e-01 0.33859 5.403e-02
## pathogenstrain      0.7985483 0.9035654 0.7089 6.322e-06 0.01760 5.689e-01
## passagenumber       0.6040298 0.0001338 0.9479 1.223e-02 0.07891 8.438e-05

test$cor_heatmap

sus_colors <- list(
    "resistant" = "#8563a7",
    "sensitive" = "#8d0000",
    "ambiguous" = "#cbcbcb",
    "unknown" = "#000000")
sus_expt <- set_expt_conditions(lp_expt, fact = "sus_category") %>%
  set_expt_batches(fact = "zymodemecategorical")

test <- set_expt_colors(sus_expt, sus_colors)


sus_norm <- normalize_expt(sus_expt, transform = "log2", convert = "cpm",
                           norm = "quant", filter = TRUE)

## Removing 142 low-count genes (8568 remaining).

## transform_counts: Found 2 values equal to 0, adding 1 to the matrix.

sus_pca <- plot_pca(sus_norm, plot_title = "PCA of parasite expression values",
                    plot_labels = FALSE)
pp(file = "images/sus_norm_pca.png", image = sus_pca[["plot"]])

sus_nb <- normalize_expt(sus_expt, transform = "log2", convert = "cpm",
                         batch = "svaseq", filter = TRUE)

## Removing 142 low-count genes (8568 remaining).

## batch_counts: Before batch/surrogate estimation, 989 entries are x==0: 0%.

## batch_counts: Before batch/surrogate estimation, 3326 entries are 0<x<1: 1%.

## Setting 222 low elements to zero.

## transform_counts: Found 222 values equal to 0, adding 1 to the matrix.

sus_nb_pca <- plot_pca(sus_nb, plot_title = "PCA of parasite expression values",
                       plot_labels = FALSE)
pp(file = "images/sus_nb_pca.png", image = sus_nb_pca[["plot"]])

At this time, we do not have very many samples, so the set of metrics/plots is fairly limited. There is really only one factor in the metadata which we can use for performing differential expression analyses, the ‘zymodeme’.

6 Zymodeme analyses

The following sections perform a series of analyses which seek to elucidate differences between the zymodemes 2.2 and 2.3 either through differential expression or variant profiles.

6.1 Differential expression

6.1.1 With respect to zymodeme attribution

TODO: Do this with and without sva and compare the results.

zy_expt <- subset_expt(lp_expt, subset = "condition=='z2.2'|condition=='z2.3'")

## subset_expt(): There were 70, now there are 34 samples.

zy_norm <- normalize_expt(zy_expt, filter = TRUE, convert = "cpm", norm = "quant")

## Removing 166 low-count genes (8544 remaining).

zy_de_nobatch <- sm(all_pairwise(zy_expt, filter = TRUE, model_batch = "svaseq"))
zy_de <- sm(all_pairwise(zy_expt, filter = TRUE, model_batch = "svaseq"))
zy_table <- sm(combine_de_tables(zy_de, excel = glue::glue("excel/zy_tables-v{ver}.xlsx")))
zy_sig <- sm(extract_significant_genes(zy_table, excel = glue::glue("excel/zy_sig-v{ver}.xlsx")))

6.1.2 Images of zymodeme DE

pp(file = "images/zymo_ma.png", image = zy_table[["plots"]][["z23_vs_z22"]][["deseq_ma_plots"]][["plot"]])

6.2 With respect to cure/failure

In contrast, we can search for genes which are differentially expressed with respect to cure/failure status.

cf_de <- sm(all_pairwise(cf_expt, filter = TRUE, model_batch = "svaseq"))

cf_table <- sm(combine_de_tables(cf_de, excel = glue::glue("excel/cf_tables-v{ver}.xlsx")))
cf_sig <- sm(extract_significant_genes(cf_table, excel = glue::glue("excel/cf_sig-v{ver}.xlsx")))

6.3 With respect to susceptibility

Finally, we can use our category of susceptibility and look for genes which change from sensitive to resistant. Keep in mind, though, that for the moment we have a lot of ambiguous and unknown strains.

sus_de <- sm(all_pairwise(sus_expt, filter = TRUE, model_batch = "svaseq"))

sus_table <- sm(combine_de_tables(sus_de, excel = glue::glue("excel/sus_tables-v{ver}.xlsx")))
sus_sig <- sm(extract_significant_genes(sus_table, excel = glue::glue("excel/sus_sig-v{ver}.xlsx")))

knitr::kable(head(sus_sig$deseq$ups$sensitive_vs_resistant, n = 20))

	gid	annotgeneproduct	annotgenetype	chromosome	start	end	strand	annotstrand	annotchromosome	annotcdslength	length	deseq_logfc	deseq_adjp	edger_logfc	edger_adjp	limma_logfc	limma_adjp	basic_nummed	basic_denmed	basic_numvar	basic_denvar	basic_logfc	basic_t	basic_p	basic_adjp	deseq_basemean	deseq_lfcse	deseq_stat	ebseq_fc	ebseq_logfc	ebseq_c1mean	ebseq_c2mean	ebseq_mean	ebseq_var	ebseq_postfc	ebseq_ppee	ebseq_ppde	ebseq_adjp	edger_logcpm	edger_lr	edger_p	limma_ave	limma_t	limma_b	limma_p	limma_adjp_ihw	deseq_adjp_ihw	edger_adjp_ihw	ebseq_adjp_ihw	basic_adjp_ihw	lfc_meta	lfc_var	lfc_varbymed	p_meta	p_var
LPAL13_000044900	LPAL13_000044900	actin-related protein 2, putative	protein coding	LPAL13_SCAF000645	507	1685	-	reverse	Not Assigned	1179.0	1178	28.310	0e+00	13.450	0.0000	9.1070	0.2437	3.9690	-4.1720	15.754	0.1283	8.141	10.160	0.0000	0.0000	858.70	1.1810	23.960	117202.52	16.839	0.0000	1172.015	813.899	5.036e+05	330.256	1.0000	0e+00	1.0000	5.0000	56.74	0e+00	1.4520	1.603	-4.2930	0.1136	2.445e-01	5.558e-123	6.257e-11	0.000e+00	7.112e-08	14.150	8.959e+00	6.329e-01	3.787e-02	4.302e-03
LPAL13_000035800	LPAL13_000035800	hypothetical protein	protein coding	LPAL13_SCAF000500	737	1006	-	reverse	Not Assigned	270.0	269	14.870	0e+00	14.070	0.0000	10.4000	0.2983	5.3200	-3.9370	15.228	0.3932	9.258	11.530	0.0000	0.0000	2938.00	1.1720	12.690	29230.09	14.835	0.1384	4339.122	3013.322	1.388e+07	1218.932	0.0000	0e+00	0.0000	6.7700	84.28	0e+00	2.3910	1.446	-4.4250	0.1527	4.223e-01	2.867e-33	3.683e-16	0.000e+00	9.311e-09	15.970	7.884e+00	4.936e-01	5.090e-02	7.772e-03
LPAL13_320026300	LPAL13_320026300	hypothetical protein, conserved	protein coding	LpaL13_32	754268	755485	-	reverse	32	1218.0	1217	14.060	0e+00	13.250	0.0000	9.8700	0.3157	4.7870	-4.0020	18.217	0.6715	8.789	9.890	0.0000	0.0000	1552.00	1.1420	12.310	16393.05	14.001	0.1294	2285.903	1587.472	2.058e+06	622.804	0.0000	0e+00	0.0000	5.8510	73.68	0e+00	2.1190	1.400	-4.4620	0.1661	3.124e-01	2.373e-31	3.939e-14	0.000e+00	5.456e-08	12.340	1.164e-01	9.438e-03	5.537e-02	9.196e-03
LPAL13_000053200	LPAL13_000053200	hypothetical protein	protein coding	LPAL13_SCAF000804	5037	5249	-	reverse	Not Assigned	213.0	212	8.847	0e+00	10.250	0.0000	5.8640	0.0345	1.0040	-4.1720	9.054	0.1283	5.176	8.466	0.0000	0.0000	76.55	1.1180	7.915	12683.81	13.631	0.0000	126.828	88.075	7.967e+03	36.435	1.0000	0e+00	1.0000	1.5600	49.10	0e+00	-0.8649	2.777	-2.9970	0.0071	3.422e-02	1.764e-12	1.145e-09	0.000e+00	1.092e-06	8.176	8.389e-02	1.026e-02	2.361e-03	1.672e-05
LPAL13_000051300	LPAL13_000051300	hypothetical protein, conserved	protein coding	LPAL13_SCAF000772	11	2344	+	forward	Not Assigned	2334.0	2333	8.358	0e+00	9.303	0.0000	3.8240	0.2550	0.2392	-3.9740	10.240	0.5654	4.213	6.206	0.0000	0.0000	138.30	1.2740	6.560	1623.37	10.665	0.0951	170.535	118.456	6.846e+04	53.119	0.0000	0e+00	0.0000	2.4210	29.89	0e+00	-1.0680	1.570	-4.3230	0.1211	2.551e-01	1.216e-08	3.080e-06	0.000e+00	4.597e-05	7.011	2.071e+00	2.954e-01	4.037e-02	4.888e-03
LPAL13_000017600	LPAL13_000017600	hypothetical protein, conserved	protein coding	LPAL13_SCAF000146	359	586	+	forward	Not Assigned	228.0	227	6.566	0e+00	6.547	0.0000	5.9330	0.0833	4.4480	-1.2190	4.355	2.8119	5.666	8.643	0.0000	0.0000	628.20	0.6955	9.441	80.11	6.324	12.0678	967.574	675.614	3.961e+05	63.578	0.0000	1e+00	0.0000	4.5480	54.14	0e+00	2.3880	2.306	-3.3600	0.0242	1.191e-01	1.019e-17	1.364e-10	9.176e-01	1.268e-06	6.766	2.103e+00	3.109e-01	8.050e-03	1.944e-04
LPAL13_000040700	LPAL13_000040700	hypothetical protein, conserved	protein coding	LPAL13_SCAF000598	54	1067	+	forward	Not Assigned	1014.0	1013	6.558	0e+00	7.957	0.0000	3.0190	0.0829	-1.2480	-4.1720	6.491	0.1283	2.923	5.613	0.0000	0.0002	20.55	1.1800	5.557	2601.36	11.345	0.0000	26.004	18.058	4.051e+02	7.897	1.0000	0e+00	1.0000	-0.1262	28.95	0e+00	-2.3590	2.309	-3.6060	0.0240	8.201e-02	1.917e-06	4.657e-06	0.000e+00	2.261e-04	5.728	1.196e+00	2.089e-01	8.003e-03	1.922e-04
LPAL13_300029400	LPAL13_300029400	hypothetical protein, conserved	protein coding	LpaL13_30	853953	854150	-	reverse	30	198.0	197	6.169	0e+00	6.102	0.0000	4.8680	0.0042	1.7290	-2.3910	1.488	1.7754	4.120	8.766	0.0000	0.0000	90.87	0.7525	8.198	59.50	5.895	2.0963	125.320	87.668	9.233e+03	22.842	0.0000	1e+00	0.0000	1.7520	47.86	0e+00	0.0911	3.752	-1.0820	0.0004	4.212e-03	3.350e-13	1.785e-09	8.838e-01	6.533e-06	5.860	4.150e-01	7.082e-02	1.221e-04	4.470e-08
LPAL13_000011700	LPAL13_000011700	hypothetical protein	protein coding	LPAL13_SCAF000076	101	364	-	reverse	Not Assigned	264.0	263	5.905	1e-04	7.455	0.0000	2.6870	0.0504	-1.3930	-4.1720	6.742	0.1283	2.779	5.239	0.0000	0.0004	14.11	1.2890	4.581	2444.21	11.255	0.0000	24.432	16.967	4.690e+02	7.590	1.0000	0e+00	1.0000	-0.5868	23.32	0e+00	-2.9030	2.580	-3.2820	0.0121	5.072e-02	1.116e-04	4.581e-05	0.000e+00	4.319e-04	5.160	1.655e+00	3.208e-01	4.025e-03	4.854e-05
LPAL13_080010600	LPAL13_080010600	hypothetical protein, conserved	protein coding	LpaL13_08	195555	195749	-	reverse	8	195.0	194	5.774	0e+00	7.291	0.0000	2.3560	0.0586	-1.8800	-4.1720	4.901	0.1283	2.292	5.029	0.0000	0.0005	11.19	1.1660	4.954	1847.09	10.851	0.0000	18.461	12.820	4.800e+02	6.130	1.0000	0e+00	1.0000	-0.9234	24.49	0e+00	-3.1040	2.502	-3.4150	0.0148	5.863e-02	3.267e-05	3.031e-05	0.000e+00	6.681e-04	4.688	2.810e+00	5.995e-01	4.920e-03	7.261e-05
LPAL13_040019400	LPAL13_040019400	hypothetical protein	protein coding	LpaL13_04	440768	441127	-	reverse	4	360.0	359	5.665	0e+00	5.547	0.0000	3.4780	0.0263	-0.4351	-3.4850	1.758	1.0862	3.050	7.418	0.0000	0.0000	34.01	0.9723	5.827	48.41	5.597	0.6939	34.070	23.872	1.800e+03	8.761	0.0000	0e+00	0.0000	0.3889	28.41	0e+00	-1.6670	2.915	-2.8310	0.0048	3.758e-02	7.294e-07	6.064e-06	0.000e+00	8.857e-06	4.958	3.756e-02	7.575e-03	1.605e-03	7.728e-06
LPAL13_200050100	LPAL13_200050100	hypothetical protein	protein coding	LpaL13_20.1	1627529	1627717	+	forward	20.1	189.0	188	5.513	0e+00	5.463	0.0000	4.7340	0.0024	2.4580	-1.9700	1.008	2.4447	4.428	8.642	0.0000	0.0000	118.50	0.6171	8.934	26.30	4.717	7.3797	194.358	137.226	2.167e+04	18.302	0.0000	1e+00	0.0000	2.1670	54.24	0e+00	0.8180	4.011	-0.3392	0.0002	2.416e-03	7.046e-16	1.364e-10	8.708e-01	3.310e-05	5.220	8.145e-01	1.560e-01	5.103e-05	7.813e-09
LPAL13_350011800	LPAL13_350011800	hypothetical protein, conserved	protein coding	LpaL13_35	171009	171242	+	forward	35	234.0	233	5.141	0e+00	5.126	0.0000	4.3400	0.0062	2.8760	-0.8627	2.424	0.1736	3.739	11.140	0.0000	0.0000	178.20	0.5811	8.847	31.92	4.997	9.4333	301.448	212.221	5.943e+04	24.086	0.0000	1e+00	0.0000	2.7240	54.09	0e+00	1.2480	3.584	-0.8512	0.0006	6.229e-03	1.282e-15	1.364e-10	9.176e-01	4.879e-09	4.952	7.332e-01	1.481e-01	2.108e-04	1.333e-07
LPAL13_080010800	LPAL13_080010800	hypothetical protein	protein coding	LpaL13_08	199409	199792	-	reverse	8	384.0	383	5.012	1e-04	6.449	0.0001	1.6610	0.2389	-2.3550	-4.1720	4.137	0.1283	1.817	4.316	0.0002	0.0023	10.46	1.0880	4.608	1048.69	10.034	0.0000	10.477	7.276	1.077e+02	3.599	1.0000	0e+00	1.0000	-0.8685	22.29	0e+00	-3.0780	1.618	-4.2920	0.1102	2.393e-01	1.006e-04	6.986e-05	0.000e+00	2.524e-03	3.942	3.004e+00	7.622e-01	3.674e-02	4.048e-03
LPAL13_170014500	LPAL13_170014500	hypothetical protein, conserved	protein coding	LpaL13_17	361708	362040	+	forward	17	333.0	332	4.932	1e-04	4.711	0.0012	2.8030	0.0333	-0.6524	-3.1970	6.988	1.5170	2.544	3.938	0.0004	0.0038	21.46	1.0430	4.730	43.02	5.427	1.0218	44.379	31.131	1.643e+03	10.389	0.0000	0e+00	0.0000	-0.2584	15.30	1e-04	-2.3840	2.796	-2.9090	0.0067	3.341e-02	6.295e-05	1.234e-03	0.000e+00	3.646e-03	4.132	5.989e-02	1.450e-02	2.273e-03	1.487e-05
LPAL13_000011800	LPAL13_000011800	hypothetical protein, conserved	protein coding	LPAL13_SCAF000076	446	640	-	reverse	Not Assigned	195.0	194	4.806	2e-04	5.382	0.0004	0.9836	0.4742	-2.4970	-3.9580	3.651	0.6042	1.461	3.260	0.0025	0.0153	11.25	1.0820	4.441	56.34	5.816	0.1523	9.134	6.389	7.337e+01	2.967	0.9995	5e-04	0.9995	-0.8436	17.82	0e+00	-3.0280	1.041	-4.6760	0.3014	6.606e-01	1.913e-04	4.376e-04	1.114e-02	1.713e-02	3.267	3.339e+00	1.022e+00	1.005e-01	3.028e-02
LPAL13_000014000	LPAL13_000014000	hypothetical protein	protein coding	LPAL13_SCAF000119	655	942	+	forward	Not Assigned	288.0	287	4.413	0e+00	4.400	0.0000	4.0190	0.0151	2.4340	-1.2390	1.518	1.8989	3.673	7.604	0.0000	0.0000	130.40	0.5404	8.166	19.75	4.304	9.7345	192.485	136.644	1.297e+04	14.826	0.0000	1e+00	0.0000	2.3000	49.02	0e+00	1.1140	3.185	-1.7980	0.0022	1.518e-02	3.350e-13	1.145e-09	9.176e-01	3.693e-05	4.411	8.730e-01	1.979e-01	7.287e-04	1.593e-06
LPAL13_000026500	LPAL13_000026500	hypothetical protein	protein coding	LPAL13_SCAF000301	144	494	-	reverse	Not Assigned	351.0	350	4.293	0e+00	4.241	0.0001	2.5410	0.1555	0.1369	-2.4930	5.421	2.0348	2.630	4.149	0.0003	0.0028	44.64	0.8060	5.326	21.34	4.415	2.5893	55.452	39.299	1.544e+03	9.519	0.0000	0e+00	0.0000	0.9069	22.12	0e+00	-0.8699	1.921	-3.9520	0.0590	1.557e-01	5.506e-06	7.424e-05	0.000e+00	2.670e-03	3.646	2.689e-02	7.375e-03	1.966e-02	1.159e-03
LPAL13_000035500	LPAL13_000035500	hypothetical protein, conserved	protein coding	LPAL13_SCAF000492	7045	7410	+	forward	Not Assigned	366.0	365	4.211	0e+00	4.212	0.0000	3.7780	0.0333	4.5240	0.8413	2.356	0.6018	3.683	9.543	0.0000	0.0000	518.90	0.6035	6.977	18.47	4.207	48.2560	891.445	633.804	3.430e+05	17.782	0.0000	1e+00	0.0000	4.2780	35.09	0e+00	2.8460	2.797	-2.3710	0.0067	3.335e-02	9.969e-10	3.974e-07	9.176e-01	2.696e-08	4.168	7.708e-01	1.849e-01	2.234e-03	1.497e-05
LPAL13_220019500	LPAL13_220019500	hypothetical protein	protein coding	LpaL13_22	578260	578538	+	forward	22	279.0	278	3.915	0e+00	3.913	0.0000	3.0880	0.0423	3.5420	0.2509	2.124	0.7532	3.291	8.402	0.0000	0.0000	289.60	0.5056	7.744	15.50	3.955	27.6226	428.407	305.945	7.136e+04	14.131	0.0000	1e+00	0.0000	3.4440	45.27	0e+00	2.3790	2.676	-2.6320	0.0093	4.198e-02	7.595e-12	5.076e-09	8.708e-01	3.683e-07	3.826	4.090e-01	1.069e-01	3.112e-03	2.906e-05

knitr::kable(head(sus_sig$deseq$downs$sensitive_vs_resistant, n = 20))

	gid	annotgeneproduct	annotgenetype	chromosome	start	end	strand	annotgenename	annotstrand	annotchromosome	annotcdslength	length	deseq_logfc	deseq_adjp	edger_logfc	edger_adjp	limma_logfc	limma_adjp	basic_nummed	basic_denmed	basic_numvar	basic_denvar	basic_logfc	basic_t	basic_adjp	deseq_basemean	deseq_lfcse	deseq_stat	deseq_p	ebseq_fc	ebseq_logfc	ebseq_c1mean	ebseq_c2mean	ebseq_mean	ebseq_var	ebseq_postfc	ebseq_ppee	ebseq_ppde	ebseq_adjp	edger_logcpm	edger_lr	edger_p	limma_ave	limma_t	limma_b	limma_p	limma_adjp_ihw	deseq_adjp_ihw	edger_adjp_ihw	ebseq_adjp_ihw	basic_adjp_ihw	lfc_meta	lfc_var	lfc_varbymed	p_meta	p_var
LPAL13_000033300	LPAL13_000033300	hypothetical protein, conserved	protein coding	LPAL13_SCAF000463	551	811	+		forward	Not Assigned	261.0	260	-5.366	0.0006	-5.252	0.0016	-6.005	0.0000	-3.7290	3.4740	10.5855	0.0633	-7.202	-10.990	0e+00	127.700	1.3070	-4.106	0.0000	0.1238	-3.013	311.93	38.622	122.132	2.245e+04	0.1327	0.0000	0.0000	0.0000	2.2460	14.750	0.0001	-1.1070	-5.720	5.0450	0e+00	3.109e-05	7.620e-04	1.557e-03	0.000e+00	2.310e-08	-5.541	0.000e+00	0.000e+00	5.432e-05	3.885e-09
LPAL13_000038400	LPAL13_000038400	expression-site associated gene (esag3), putative	protein coding	LPAL13_SCAF000573	101	1360	+		forward	Not Assigned	1260.0	1259	-2.987	0.0000	-2.981	0.0000	-3.311	0.0001	4.6320	8.2380	3.1197	0.0291	-3.606	-10.100	0e+00	3589.000	0.5604	-5.329	0.0000	0.1737	-2.526	8823.76	1532.438	3760.342	1.554e+07	0.1785	0.0000	0.0000	0.0000	7.0530	31.760	0.0000	5.7730	-5.315	5.1220	0e+00	8.555e-05	5.448e-06	1.508e-06	0.000e+00	7.112e-08	-3.046	2.268e-02	-7.444e-03	4.680e-07	5.059e-13
LPAL13_350063000	LPAL13_350063000	hypothetical protein	protein coding	LpaL13_35	1964328	1964543	-		reverse	35	216.0	215	-2.831	0.0000	-2.804	0.0000	-3.432	0.0000	-2.3300	1.2080	2.1382	0.2275	-3.538	-10.860	0e+00	20.770	0.4869	-5.813	0.0000	0.1384	-2.853	55.15	7.623	22.146	6.307e+02	0.1595	0.0000	1.0000	0.0000	-0.3699	32.430	0.0000	-1.4710	-6.977	8.0100	0e+00	1.358e-06	6.482e-07	1.165e-06	8.838e-01	4.879e-09	-3.042	6.226e-03	-2.047e-03	6.694e-09	2.932e-17
LPAL13_140019300	LPAL13_140019300	bt1 family, putative	protein coding	LpaL13_14	530784	531350	+		forward	14	567.0	566	-2.670	0.0000	-2.666	0.0000	-2.508	0.0000	4.6450	7.0660	0.4797	1.1123	-2.420	-6.978	2e-04	1818.000	0.3821	-6.989	0.0000	0.1702	-2.555	4611.25	784.787	1953.984	5.164e+06	0.1758	0.0000	1.0000	0.0000	6.0720	56.420	0.0000	5.3600	-6.856	11.0800	0e+00	1.496e-06	9.490e-10	6.257e-11	1.000e+00	1.499e-04	-2.652	1.598e-01	-6.026e-02	8.713e-10	2.270e-18
LPAL13_000012000	LPAL13_000012000	hypothetical protein	protein coding	LPAL13_SCAF000080	710	1159	-		reverse	Not Assigned	450.0	449	-2.643	0.0007	-2.634	0.0003	-3.063	0.0036	0.0950	3.9560	7.6621	0.1804	-3.861	-6.796	0e+00	203.300	0.6482	-4.077	0.0000	0.2237	-2.160	451.41	100.978	208.054	4.893e+04	0.2351	0.1874	0.8126	0.1874	2.9190	18.660	0.0000	1.3190	-3.821	0.2633	3e-04	3.601e-03	8.461e-04	3.059e-04	8.579e-01	1.862e-05	-2.788	1.668e-02	-5.981e-03	1.174e-04	2.285e-08
LPAL13_310035500	LPAL13_310035500	hypothetical protein	protein coding	LpaL13_31	1198439	1198957	-		reverse	31	519.0	518	-2.628	0.0033	-2.493	0.0023	-3.214	0.0000	-4.1830	-0.4027	4.0925	0.4977	-3.780	-8.269	0e+00	7.018	0.7348	-3.576	0.0003	0.2939	-1.767	18.43	5.409	9.386	3.219e+02	0.3477	0.0000	0.0000	0.0000	-1.9350	13.780	0.0002	-3.1660	-7.180	6.1600	0e+00	7.301e-07	3.277e-03	2.291e-03	0.000e+00	3.375e-07	-2.778	0.000e+00	0.000e+00	1.846e-04	3.067e-08
LPAL13_310039200	LPAL13_310039200	hypothetical protein	protein coding	LpaL13_31	1301745	1301972	-		reverse	31	228.0	227	-2.429	0.0000	-2.425	0.0000	-2.486	0.0000	1.2200	3.7790	1.3494	0.2183	-2.559	-9.417	0e+00	188.800	0.4143	-5.864	0.0000	0.2457	-2.025	396.35	97.358	188.717	3.434e+04	0.2570	0.4442	0.5558	0.4442	2.8160	38.010	0.0000	1.9640	-5.821	6.9370	0e+00	3.275e-05	5.090e-07	1.181e-07	5.203e-01	2.310e-08	-2.476	8.014e-02	-3.237e-02	6.034e-08	1.000e-14
LPAL13_000012100	LPAL13_000012100	hypothetical protein	protein coding	LPAL13_SCAF000080	1637	1894	-		reverse	Not Assigned	258.0	257	-2.286	0.0082	-2.272	0.0075	-3.355	0.0003	-2.2140	1.2000	6.2602	0.6808	-3.414	-6.109	0e+00	30.200	0.7042	-3.246	0.0012	0.2746	-1.865	66.01	18.121	32.755	1.804e+03	0.3055	0.0537	0.9463	0.0537	0.2122	10.880	0.0010	-1.4340	-4.809	2.2850	0e+00	3.152e-04	8.203e-03	7.497e-03	8.335e-01	4.173e-05	-2.689	7.115e-02	-2.646e-02	7.163e-04	3.850e-07
LPAL13_340039600	LPAL13_340039600	hypothetical protein	protein coding	LpaL13_34	1247554	1247757	-		reverse	34	204.0	203	-2.241	0.0002	-2.237	0.0001	-2.628	0.0015	1.2500	4.2050	3.6080	0.0559	-2.955	-7.645	0e+00	218.200	0.5128	-4.369	0.0000	0.2254	-2.149	518.32	116.821	239.500	4.536e+04	0.2307	0.0000	1.0000	0.0000	3.0090	21.460	0.0000	1.9570	-4.190	1.3890	1e-04	1.508e-03	2.494e-04	9.710e-05	9.635e-01	4.535e-06	-2.376	8.498e-03	-3.576e-03	3.288e-05	1.872e-09
LPAL13_310031000	LPAL13_310031000	hypothetical protein, conserved	protein coding	LpaL13_31	1075172	1075459	-		reverse	31	288.0	287	-2.221	0.0000	-2.201	0.0000	-2.810	0.0000	-2.0060	0.9976	3.5024	0.5671	-3.003	-6.860	0e+00	26.100	0.4570	-4.860	0.0000	0.2698	-1.890	55.87	15.064	27.532	1.035e+03	0.2951	0.1254	0.8746	0.1254	0.0381	23.870	0.0000	-1.1800	-5.973	5.4530	0e+00	1.497e-05	3.843e-05	3.755e-05	8.682e-01	6.085e-06	-2.400	6.650e-04	-2.772e-04	7.662e-07	3.423e-13
LPAL13_000038500	LPAL13_000038500	hypothetical protein	protein coding	LPAL13_SCAF000575	39	251	+		forward	Not Assigned	213.0	212	-2.098	0.0050	-2.083	0.0077	-3.311	0.0001	-1.9360	1.4300	4.6504	0.6757	-3.367	-6.768	0e+00	31.310	0.6124	-3.427	0.0006	0.2833	-1.820	77.47	21.939	38.906	2.414e+03	0.3096	0.1593	0.8407	0.1593	0.2145	10.810	0.0010	-1.3130	-5.467	4.1160	0e+00	5.635e-05	4.994e-03	7.747e-03	8.406e-01	6.533e-06	-2.471	1.211e-01	-4.903e-02	5.407e-04	2.584e-07
LPAL13_310031300	LPAL13_310031300	hypothetical protein, conserved	protein coding	LpaL13_31	1084772	1085059	-		reverse	31	288.0	287	-2.033	0.0047	-2.029	0.0032	-3.046	0.0004	-1.0710	2.0840	3.9543	0.7623	-3.155	-6.616	0e+00	61.360	0.5900	-3.446	0.0006	0.2465	-2.020	130.45	32.149	62.187	5.901e+03	0.2666	0.0529	0.9471	0.0529	1.1930	12.960	0.0003	-0.2414	-4.723	2.5090	0e+00	5.553e-04	4.724e-03	3.223e-03	8.478e-01	8.857e-06	-2.305	3.960e-02	-1.718e-02	3.001e-04	7.796e-08
LPAL13_050005000	LPAL13_050005000	hypothetical protein	protein coding	LpaL13_05	3394	3612	-		reverse	5	219.0	218	-1.983	0.0077	-1.977	0.0046	-2.732	0.0002	0.2033	2.6750	2.0316	0.1724	-2.472	-7.940	0e+00	88.260	0.6063	-3.271	0.0011	0.2820	-1.826	177.99	50.188	89.238	6.186e+03	0.2912	0.0006	0.9994	0.0006	1.7080	12.080	0.0005	0.4586	-5.053	3.9660	0e+00	2.371e-04	9.310e-03	4.591e-03	8.708e-01	6.620e-07	-2.227	1.857e-02	-8.335e-03	5.284e-04	2.851e-07
LPAL13_140019100	LPAL13_140019100	bt1 family, putative	protein coding	LpaL13_14	525164	525514	+		forward	14	351.0	350	-1.975	0.0000	-1.972	0.0000	-2.055	0.0000	3.9170	5.9980	0.3507	0.5490	-2.081	-8.232	0e+00	857.500	0.3048	-6.479	0.0000	0.2333	-2.100	1937.62	451.966	905.916	6.953e+05	0.2374	0.0000	1.0000	0.0000	4.9890	50.690	0.0000	4.5600	-7.326	12.9600	0e+00	5.315e-07	1.926e-08	5.922e-10	9.176e-01	2.350e-05	-1.982	9.112e-03	-4.598e-03	1.551e-10	3.741e-20
LPAL13_340039700	LPAL13_340039700	snare domain containing protein, putative	protein coding	LpaL13_34	1248192	1248947	-		reverse	34	756.0	755	-1.781	0.0000	-1.778	0.0000	-1.882	0.0000	4.6130	6.6510	0.6868	0.0521	-2.038	-11.360	0e+00	1351.000	0.3095	-5.753	0.0000	0.2859	-1.806	2810.80	803.693	1416.976	1.132e+06	0.2899	0.0000	1.0000	0.0000	5.6450	38.840	0.0000	5.2460	-6.273	8.7710	0e+00	7.177e-06	8.329e-07	8.056e-08	9.573e-01	4.879e-09	-1.773	2.901e-02	-1.636e-02	1.256e-08	2.072e-16
LPAL13_170015400	LPAL13_170015400	hypothetical protein, conserved	protein coding	LpaL13_17	395975	396307	+		forward	17	333.0	332	-1.674	0.0000	-1.669	0.0000	-1.669	0.0002	1.2440	3.2670	0.9459	0.1363	-2.023	-9.027	0e+00	148.400	0.2999	-5.584	0.0000	0.3146	-1.669	270.10	84.958	141.528	1.297e+04	0.3199	0.0000	1.0000	0.0000	2.4610	31.800	0.0000	1.9810	-5.001	4.0120	0e+00	1.920e-04	1.774e-06	1.495e-06	8.708e-01	6.699e-08	-1.685	3.478e-02	-2.064e-02	1.442e-06	6.065e-12
LPAL13_140019200	LPAL13_140019200	inositol-3-phosphate synthase	protein coding	LpaL13_14	527711	529291	+	INO1	forward	14	1581.0	1580	-1.465	0.0000	-1.461	0.0000	-1.529	0.0000	8.8250	10.3900	0.1718	0.4796	-1.566	-6.969	2e-04	18910.000	0.2607	-5.619	0.0000	0.3510	-1.510	36839.52	12931.847	20236.970	1.798e+08	0.3540	0.0000	1.0000	0.0000	9.4520	45.990	0.0000	9.2330	-6.630	10.2000	0e+00	3.648e-06	1.506e-06	3.767e-09	1.000e+00	2.363e-04	-1.541	2.454e-02	-1.592e-02	8.612e-09	9.489e-17
LPAL13_320038700	LPAL13_320038700	hypothetical protein, conserved	protein coding	LpaL13_32	1175024	1175257	+		forward	32	234.0	233	-1.426	0.0000	-1.421	0.0000	-1.458	0.0000	2.5500	3.9570	0.4259	0.1120	-1.407	-8.529	0e+00	255.900	0.2296	-6.211	0.0000	0.4144	-1.271	436.05	180.702	258.724	2.162e+04	0.4183	0.0011	0.9989	0.0011	3.2490	40.400	0.0000	3.0040	-6.105	8.1100	0e+00	1.204e-05	8.363e-08	4.223e-08	8.838e-01	2.066e-07	-1.482	2.663e-02	-1.797e-02	1.899e-08	1.040e-15
LPAL13_040007800	LPAL13_040007800	hypothetical protein, conserved	protein coding	LpaL13_04	77524	78306	+		forward	4	783.0	782	-1.387	0.0000	-1.383	0.0000	-1.273	0.0000	6.5520	7.7820	0.1432	0.3791	-1.230	-6.135	6e-04	4045.000	0.2359	-5.881	0.0000	0.3806	-1.394	7003.17	2665.491	3990.892	7.653e+06	0.3857	0.0001	0.9999	0.0001	7.2260	43.070	0.0000	7.0020	-5.799	6.9070	0e+00	2.572e-05	4.795e-07	1.328e-08	1.000e+00	6.587e-04	-1.374	6.214e-02	-4.523e-02	6.531e-08	1.200e-14
LPAL13_350013200	LPAL13_350013200	hypothetical protein, conserved	protein coding	LpaL13_35	223837	224070	+		forward	35	234.0	233	-1.377	0.0114	-1.363	0.0201	-2.035	0.0003	-2.0610	-0.1712	1.3327	0.7337	-1.890	-5.455	3e-04	10.700	0.4406	-3.126	0.0018	0.3587	-1.479	24.88	8.918	13.797	2.950e+02	0.3915	0.7783	0.2217	0.7783	-1.1510	8.503	0.0035	-2.0600	-4.819	1.7080	0e+00	3.139e-04	1.141e-02	2.008e-02	2.557e-01	2.467e-04	-1.577	3.478e-02	-2.205e-02	1.776e-03	3.127e-06

sus_ma <- sus_table[["plots"]][["sensitive_vs_resistant"]][["deseq_ma_plots"]][["plot"]]
pp(file = "images/sus_ma.png", image = sus_ma)

## test <- ggplt(sus_ma)

6.4 Ontology searches

Now let us look for ontology categories which are increased in the 2.3 samples followed by the 2.2 samples.

## Gene categories more represented in the 2.3 group.
zy_go_up <- sm(simple_goseq(sig_genes = zy_sig[["deseq"]][["ups"]][[1]],
                            go_db = lp_go, length_db = lp_lengths))

## Gene categories more represented in the 2.2 group.
zy_go_down <- sm(simple_goseq(sig_genes = zy_sig[["deseq"]][["downs"]][[1]],
                              go_db = lp_go, length_db = lp_lengths))

6.4.1 A couple plots from the differential expression

6.4.1.1 Number of genes in agreement among DE methods, 2.3 more than 2.2

In the function ‘combined_de_tables()’ above, one of the tasks performed is to look at the agreement among DESeq2, limma, and edgeR. The following show a couple of these for the set of genes observed with a fold-change >= |2| and adjusted p-value <= 0.05.

zy_table[["venns"]][[1]][["p_lfc1"]][["up_noweight"]]

6.4.1.2 Number of genes in agreement among DE methods, 2.2 more than 2.3

zy_table[["venns"]][[1]][["p_lfc1"]][["down_noweight"]]

6.4.1.3 goseq ontology plots of groups of genes, 2.3 more than 2.2

zy_go_up$pvalue_plots$bpp_plot_over

6.4.1.4 goseq ontology plots of groups of genes, 2.2 more than 2.3

zy_go_down$pvalue_plots$bpp_plot_over

6.5 Look for agreement between sensitivity and zymodemes

Remind myself, the data structures are (zy|sus)_(de|table|sig).

zy_df <- zy_table[["data"]][["z23_vs_z22"]]
sus_df <- sus_table[["data"]][["sensitive_vs_resistant"]]

both_df <- merge(zy_df, sus_df, by = "row.names")
plot_df <- both_df[, c("deseq_logfc.x", "deseq_logfc.y")]
rownames(plot_df) <- both_df[["Row.names"]]
colnames(plot_df) <- c("z23_vs_z22", "sensitive_vs_resistant")

compare <- plot_linear_scatter(plot_df)

## Warning in plot_multihistogram(df): NAs introduced by coercion

pp(file = "images/compare_sus_zy.png", image = compare$scatter)

compare$cor

## 
##  Pearson's product-moment correlation
## 
## data:  df[, 1] and df[, 2]
## t = -188, df = 8542, p-value <2e-16
## alternative hypothesis: true correlation is not equal to 0
## 95 percent confidence interval:
##  -0.9014 -0.8932
## sample estimates:
##     cor 
## -0.8974

6.6 Zymodeme enzyme gene IDs

Najib read me an email listing off the gene names associated with the zymodeme classification. I took those names and cross referenced them against the Leishmania panamensis gene annotations and found the following:

They are:

ALAT: LPAL13_120010900 – alanine aminotransferase
ASAT: LPAL13_340013000 – aspartate aminotransferase
G6PD: LPAL13_000054100 – glucase-6-phosphate 1-dehydrogenase
NH: LPAL13_14006100, LPAL13_180018500 – inosine-guanine nucleoside hydrolase
MPI: LPAL13_320022300 (maybe) – mannose phosphate isomerase (I chose phosphomannose isomerase)

Given these 6 gene IDs (NH has two gene IDs associated with it), I can do some looking for specific differences among the various samples.

6.6.1 Expression levels of zymodeme genes

The following creates a colorspace (red to green) heatmap showing the observed expression of these genes in every sample.

my_genes <- c("LPAL13_120010900", "LPAL13_340013000", "LPAL13_000054100",
              "LPAL13_140006100", "LPAL13_180018500", "LPAL13_320022300",
              "other")
my_names <- c("ALAT", "ASAT", "G6PD", "NHv1", "NHv2", "MPI", "other")

zymo_expt <- exclude_genes_expt(zy_norm, ids = my_genes, method = "keep")

## Before removal, there were 8544 genes, now there are 6.

## There are 34 samples which kept less than 90 percent counts.

## TMRC20001 TMRC20065 TMRC20005 TMRC20066 TMRC20039 TMRC20037 TMRC20038 TMRC20067 
##    0.1313    0.1250    0.1325    0.1059    0.1303    0.1102    0.1129    0.1165 
## TMRC20068 TMRC20041 TMRC20015 TMRC20009 TMRC20010 TMRC20016 TMRC20011 TMRC20012 
##    0.1155    0.1181    0.1147    0.1137    0.1098    0.1059    0.1103    0.1207 
## TMRC20013 TMRC20017 TMRC20014 TMRC20018 TMRC20021 TMRC20022 TMRC20077 TMRC20074 
##    0.1205    0.1064    0.1089    0.1147    0.1063    0.1310    0.1221    0.1209 
## TMRC20063 TMRC20053 TMRC20052 TMRC20064 TMRC20075 TMRC20051 TMRC20050 TMRC20049 
##    0.1169    0.1184    0.1105    0.1140    0.1111    0.1285    0.1155    0.1400 
## TMRC20062 TMRC20054 
##    0.1288    0.1279

zymo_heatmap <- plot_sample_heatmap(zymo_expt, row_label = my_names)
zymo_heatmap

6.7 Empirically observed Zymodeme genes from differential expression analysis

In contrast, the following plots take the set of genes which are shared among all differential expression methods (|lfc| >= 1.0 and adjp <= 0.05) and use them to make categories of genes which are increased in 2.3 or 2.2.

shared_zymo <- intersect_significant(zy_table)

## Deleting the file excel/intersect_significant.xlsx before writing the tables.

up_shared <- shared_zymo[["ups"]][[1]][["data"]][["all"]]
rownames(up_shared)

##  [1] "LPAL13_000033300" "LPAL13_000012000" "LPAL13_310031300" "LPAL13_000038500"
##  [5] "LPAL13_000038400" "LPAL13_000012100" "LPAL13_340039600" "LPAL13_310031000"
##  [9] "LPAL13_310039200" "LPAL13_050005000" "LPAL13_350063000" "LPAL13_210015500"
## [13] "LPAL13_140019300" "LPAL13_180013900" "LPAL13_340039700" "LPAL13_170015400"
## [17] "LPAL13_270034100" "LPAL13_350013200" "LPAL13_250006300" "LPAL13_140019100"
## [21] "LPAL13_350012400" "LPAL13_350073400" "LPAL13_330021800" "LPAL13_240009700"
## [25] "LPAL13_000052700" "LPAL13_140019200" "LPAL13_250025700" "LPAL13_320038700"
## [29] "LPAL13_330021900" "LPAL13_210005000" "LPAL13_350073200" "LPAL13_310032500"
## [33] "LPAL13_230011200" "LPAL13_310028500" "LPAL13_230011400" "LPAL13_230011500"
## [37] "LPAL13_160014500" "LPAL13_050009600" "LPAL13_230011300" "LPAL13_040007800"
## [41] "LPAL13_160014100"

upshared_expt <- exclude_genes_expt(zy_norm, ids = rownames(up_shared), method = "keep")

## Before removal, there were 8544 genes, now there are 41.

## There are 34 samples which kept less than 90 percent counts.

## TMRC20001 TMRC20065 TMRC20005 TMRC20066 TMRC20039 TMRC20037 TMRC20038 TMRC20067 
##   0.32583   0.40481   0.09692   0.35825   0.14393   0.38093   0.50866   0.29289 
## TMRC20068 TMRC20041 TMRC20015 TMRC20009 TMRC20010 TMRC20016 TMRC20011 TMRC20012 
##   0.34705   0.14461   0.39129   0.12494   0.37945   0.27684   0.13830   0.11794 
## TMRC20013 TMRC20017 TMRC20014 TMRC20018 TMRC20021 TMRC20022 TMRC20077 TMRC20074 
##   0.32652   0.13750   0.14642   0.30204   0.33880   0.11629   0.11344   0.14166 
## TMRC20063 TMRC20053 TMRC20052 TMRC20064 TMRC20075 TMRC20051 TMRC20050 TMRC20049 
##   0.12976   0.15457   0.40198   0.36990   0.30504   0.56640   0.12676   0.14631 
## TMRC20062 TMRC20054 
##   0.59300   0.49938

We can plot a quick heatmap to get a sense of the differences observed between the genes which are different between the two zymodemes.

6.7.1 Heatmap of zymodeme gene expression increased in 2.3 vs. 2.2

high_23_heatmap <- plot_sample_heatmap(upshared_expt, row_label = rownames(up_shared))
high_23_heatmap

6.7.2 Heatmap of zymodeme gene expression increased in 2.2 vs. 2.3

down_shared <- shared_zymo[["downs"]][[1]][["data"]][["all"]]
downshared_expt <- exclude_genes_expt(zy_norm, ids = rownames(down_shared), method = "keep")

## Before removal, there were 8544 genes, now there are 67.

## There are 34 samples which kept less than 90 percent counts.

## TMRC20001 TMRC20065 TMRC20005 TMRC20066 TMRC20039 TMRC20037 TMRC20038 TMRC20067 
##    0.2732    0.2311    0.7574    0.2684    0.7461    0.2422    0.2348    0.2786 
## TMRC20068 TMRC20041 TMRC20015 TMRC20009 TMRC20010 TMRC20016 TMRC20011 TMRC20012 
##    0.2430    0.7511    0.2312    0.7425    0.2165    0.2537    0.6578    0.6401 
## TMRC20013 TMRC20017 TMRC20014 TMRC20018 TMRC20021 TMRC20022 TMRC20077 TMRC20074 
##    0.2153    0.7571    0.7355    0.2065    0.2035    0.7990    0.6559    0.7732 
## TMRC20063 TMRC20053 TMRC20052 TMRC20064 TMRC20075 TMRC20051 TMRC20050 TMRC20049 
##    0.7174    0.6859    0.2162    0.2381    0.2163    0.2301    0.7039    0.8006 
## TMRC20062 TMRC20054 
##    0.2268    0.2470

high_22_heatmap <- plot_sample_heatmap(downshared_expt, row_label = rownames(down_shared))
high_22_heatmap

7 SNP profiles

Now I will combine our previous samples and our new samples in the hopes of finding variant positions which help elucidate currently unknown aspects of either group via their clustering to known samples from the other group. In other words, we do not know the zymodeme annotations for the old samples nor the strain identities (or the shortcut ‘chronic vs. self-healing’) for the new samples. I hope to make educated guesses given the variant profiles. There are some differences in how the previous and current data sets were analyzed (though I have since redone the old samples so it should be trivial to remove those differences now).

I added our 2016 data to a specific TMRC2 sample sheet, dated 20191203. Thus I will load the data here. That previous data was mapped using tophat, so I will also need to make some changes to the gene names to accomodate the two mappings.

old_expt <- sm(create_expt("sample_sheets/tmrc2_samples_20191203.xlsx",
                           file_column = "tophat2file"))

tt <- lp_expt[["expressionset"]]
rownames(tt) <- gsub(pattern = "^exon_", replacement = "", x = rownames(tt))
rownames(tt) <- gsub(pattern = "\\.E1$", replacement = "", x = rownames(tt))
lp_expt$expressionset <- tt

tt <- old_expt$expressionset
rownames(tt) <- gsub(pattern = "^exon_", replacement = "", x = rownames(tt))
rownames(tt) <- gsub(pattern = "\\.1$", replacement = "", x = rownames(tt))
old_expt$expressionset <- tt
rm(tt)

7.1 Create the SNP expressionset

One other important caveat, we have a group of new samples which have not yet run through the variant search pipeline, so I need to remove them from consideration. Though it looks like they finished overnight…

## The next line drops the samples which are missing the SNP pipeline.
lp_snp <- subset_expt(lp_expt, subset="!is.na(pData(lp_expt)[['bcftable']])")

## subset_expt(): There were 70, now there are 66 samples.

new_snps <- sm(count_expt_snps(lp_snp, annot_column = "bcftable"))
old_snps <- sm(count_expt_snps(old_expt, annot_column = "bcftable", snp_column = 2))

both_snps <- combine_expts(new_snps, old_snps)
both_norm <- sm(normalize_expt(both_snps, transform = "log2", convert = "cpm", filter = TRUE))

## strains <- both_norm[["design"]][["strain"]]
both_strain <- set_expt_conditions(both_norm, fact = "strain")

The data structure ‘both_norm’ now contains our 2016 data along with the newer data collected since 2019.

7.2 Plot of SNP profiles for zymodemes

The following plot shows the SNP profiles of all samples (old and new) where the colors at the top show either the 2.2 strains (orange), 2.3 strains (green), the previous samples (purple), or the various lab strains (pink etc).

old_new_variant_heatmap <- plot_disheat(both_norm)
pp(file = "images/raw_snp_disheat.png", image = old_new_variant_heatmap,
   height = 12, width = 12)

The function get_snp_sets() takes the provided metadata factor (in this case ‘condition’) and looks for variants which are exclusive to each element in it. In this case, this is looking for differences between 2.2 and 2.3, as well as the set shared among them.

snp_sets <- get_snp_sets(both_snps, factor = "condition")

## The factor z2.3 has 18 rows.

## The factor z2.2 has 13 rows.

## The factor unknown has 16 rows.

## The factor null has 19 rows.

## The factor sh has 13 rows.

## The factor chr has 14 rows.

## The factor inf has 6 rows.

## Iterating over 727 elements.

both_expt <- combine_expts(lp_expt, old_expt)

snp_genes <- sm(snps_vs_genes(both_expt, snp_sets, expt_name_col = "chromosome"))
## I think we have some metrics here we can plot...
snp_subset <- sm(snp_subset_genes(
  both_expt, both_snps,
  genes = c("LPAL13_120010900", "LPAL13_340013000", "LPAL13_000054100",
            "LPAL13_140006100", "LPAL13_180018500", "LPAL13_320022300")))
zymo_heat <- plot_sample_heatmap(snp_subset, row_label = rownames(exprs(snp_subset)))
zymo_heat

Didn’t I create a set of densities by chromosome? Oh I think they come in from get_snp_sets()

7.3 SNPS associated with clinical response in the TMRC samples

clinical_sets <- get_snp_sets(new_snps, factor = "clinicalresponse")

## The factor cure has 26 rows.

## The factor failure has 21 rows.

## The factor laboratory line has only 1 row.

## The factor laboratory line miltefosine resistant has only 1 row.

## The factor nd has 4 rows.

## The factor notapplicable has 9 rows.

## The factor reference strain has 4 rows.

## Iterating over 695 elements.

density_vec <- clinical_sets[["density"]]
chromosome_idx <- grep(pattern = "LpaL", x = names(density_vec))
density_df <- as.data.frame(density_vec[chromosome_idx])
density_df[["chr"]] <- rownames(density_df)
colnames(density_df) <- c("density_vec", "chr")
ggplot(density_df, aes_string(x = "chr", y = "density_vec")) +
  ggplot2::geom_col() +
  ggplot2::theme(axis.text = ggplot2::element_text(size = 10, colour = "black"),
                 axis.text.x = ggplot2::element_text(angle = 90, vjust = 0.5))

## clinical_written <- write_variants(new_snps)

7.3.1 Cross reference these variants by gene

clinical_genes <- sm(snps_vs_genes(lp_expt, clinical_sets, expt_name_col = "chromosome"))

snp_density <- merge(as.data.frame(clinical_genes[["summary_by_gene"]]),
                     as.data.frame(fData(lp_expt)),
                     by = "row.names")
snp_density <- snp_density[, c(1, 2, 4, 15)]
colnames(snp_density) <- c("name", "snps", "product", "length")
snp_density[["product"]] <- tolower(snp_density[["product"]])
snp_density[["length"]] <- as.numeric(snp_density[["length"]])
snp_density[["density"]] <- snp_density[["snps"]] / snp_density[["length"]]
snp_idx <- order(snp_density[["density"]], decreasing = TRUE)
snp_density <- snp_density[snp_idx, ]

removers <- c("amastin", "gp63", "leishmanolysin")
for (r in removers) {
  drop_idx <- grepl(pattern = r, x = snp_density[["product"]])
  snp_density <- snp_density[!drop_idx, ]
}
## Filter these for [A|a]mastin gp63 Leishmanolysin

clinical_snps <- snps_intersections(lp_expt, clinical_sets, chr_column = "chromosome")

fail_ref_snps <- as.data.frame(clinical_snps[["inters"]][["failure, reference strain"]])
cure_snps <- as.data.frame(clinical_snps[["inters"]][["cure"]])

head(fail_ref_snps)

##                                           seqnames  start    end width strand
## chr_LpaL13-13_pos_167047_ref_G_alt_C     LpaL13-13 167047 167048     2      +
## chr_LpaL13-15_pos_42885_ref_A_alt_G      LpaL13-15  42885  42886     2      +
## chr_LpaL13-20.1_pos_111781_ref_T_alt_C LpaL13-20.1 111781 111782     2      +
## chr_LpaL13-25_pos_147406_ref_G_alt_C     LpaL13-25 147406 147407     2      +
## chr_LpaL13-29_pos_649951_ref_T_alt_C     LpaL13-29 649951 649952     2      +
## chr_LpaL13-30_pos_597834_ref_T_alt_G     LpaL13-30 597834 597835     2      +

head(cure_snps)

##                                           seqnames  start    end width strand
## chr_LpaL13-08_pos_184791_ref_T_alt_A     LpaL13-08 184791 184792     2      +
## chr_LpaL13-20.1_pos_369935_ref_C_alt_T LpaL13-20.1 369935 369936     2      +
## chr_LpaL13-20.1_pos_370282_ref_C_alt_T LpaL13-20.1 370282 370283     2      +
## chr_LpaL13-20.1_pos_371356_ref_T_alt_C LpaL13-20.1 371356 371357     2      +
## chr_LpaL13-20.1_pos_380785_ref_A_alt_G LpaL13-20.1 380785 380786     2      +
## chr_LpaL13-20.1_pos_382801_ref_A_alt_C LpaL13-20.1 382801 382802     2      +

annot <- fData(lp_expt)
clinical_interest <- as.data.frame(clinical_snps[["gene_summaries"]][["cure"]])
clinical_interest <- merge(clinical_interest,
                           as.data.frame(clinical_snps[["gene_summaries"]][["failure, reference strain"]]),
                           by = "row.names")
rownames(clinical_interest) <- clinical_interest[["Row.names"]]
clinical_interest[["Row.names"]] <- NULL
colnames(clinical_interest) <- c("cure_snps","fail_snps")
annot <- merge(annot, clinical_interest, by = "row.names")
rownames(annot) <- annot[["Row.names"]]
annot[["Row.names"]] <- NULL
fData(lp_expt$expressionset) <- annot

8 Zymodeme for new samples

The heatmap produced here should show the variants only for the zymodeme genes.

8.1 Hunt for snp clusters

I am thinking that if we find clusters of locations which are variant, that might provide some PCR testing possibilities.

new_sets <- get_snp_sets(new_snps, factor = "phenotypiccharacteristics")

## The factor 22 has 13 rows.

## The factor 23 has 18 rows.

## The factor laboratory line has only 1 row.

## The factor laboratory line miltefosine resistant has only 1 row.

## The factor notapplicable has 29 rows.

## The factor reference strain has 4 rows.

## Iterating over 695 elements.

summary(new_sets)

##               Length Class      Mode     
## medians         7    data.frame list     
## possibilities   6    -none-     character
## intersections  58    -none-     list     
## chr_data      695    -none-     list     
## set_names      64    -none-     list     
## invert_names   64    -none-     list     
## density       695    -none-     numeric

## 1000000: 2.2
## 0100000: 2.3

summary(new_sets[["intersections"]][["10000"]])

## Length  Class   Mode 
##      0   NULL   NULL

summary(new_sets[["intersections"]][["01000"]])

## Length  Class   Mode 
##      0   NULL   NULL

Thus we see that there are 511 variants associated with 2.2 and 49,790 associated with 2.3.

8.1.1 A small function for searching for potential PCR primers

The following function uses the positional data to look for sequential mismatches associated with zymodeme in the hopes that there will be some regions which would provide good potential targets for a PCR-based assay.

sequential_variants <- function(snp_sets, conditions = NULL, minimum = 3, maximum_separation = 3) {
  if (is.null(conditions)) {
    conditions <- 1
  }
  intersection_sets <- snp_sets[["intersections"]]
  intersection_names <- snp_sets[["set_names"]]
  chosen_intersection <- 1
  if (is.numeric(conditions)) {
    chosen_intersection <- conditions
  } else {
    intersection_idx <- intersection_names == conditions
    chosen_intersection <- names(intersection_names)[intersection_idx]
  }

  possible_positions <- intersection_sets[[chosen_intersection]]
  position_table <- data.frame(row.names = possible_positions)
  pat <- "^chr_(.+)_pos_(.+)_ref_.*$"
  position_table[["chr"]] <- gsub(pattern = pat, replacement = "\\1", x = rownames(position_table))
  position_table[["pos"]] <- as.numeric(gsub(pattern = pat, replacement = "\\2", x = rownames(position_table)))
  position_idx <- order(position_table[, "chr"], position_table[, "pos"])
  position_table <- position_table[position_idx, ]
  position_table[["dist"]] <- 0

  last_chr <- ""
  for (r in 1:nrow(position_table)) {
    this_chr <- position_table[r, "chr"]
    if (r == 1) {
      position_table[r, "dist"] <- position_table[r, "pos"]
      last_chr <- this_chr
      next
    }
    if (this_chr == last_chr) {
      position_table[r, "dist"] <- position_table[r, "pos"] - position_table[r - 1, "pos"]
    } else {
      position_table[r, "dist"] <- position_table[r, "pos"]
    }
    last_chr <- this_chr
  }

  ## Working interactively here.
  
  doubles <- position_table[["dist"]] == 1
  doubles <- position_table[doubles, ]
  write.csv(doubles, "doubles.csv")

  one_away <- position_table[["dist"]] == 2
  one_away <- position_table[one_away, ]
  write.csv(one_away, "one_away.csv")

  two_away <- position_table[["dist"]] == 3
  two_away <- position_table[two_away, ]
  write.csv(two_away, "two_away.csv")

  combined <- rbind(doubles, one_away)
  combined <- rbind(combined, two_away)
  position_idx <- order(combined[, "chr"], combined[, "pos"])
  combined <- combined[position_idx, ]
  
  this_chr <- ""
  for (r in 1:nrow(combined)) {
    this_chr <- combined[r, "chr"]
    if (r == 1) {
      combined[r, "dist_pair"] <- combined[r, "pos"]
      last_chr <- this_chr
      next
    }
    if (this_chr == last_chr) {
      combined[r, "dist_pair"] <- combined[r, "pos"] - combined[r - 1, "pos"]
    } else {
      combined[r, "dist_pair"] <- combined[r, "pos"]
    }
    last_chr <- this_chr
  }

  dist_pair_maximum <- 1000
  dist_pair_minimum <- 200
  dist_pair_idx <- combined[["dist_pair"]] <= dist_pair_maximum &
    combined[["dist_pair"]] >= dist_pair_minimum
  remaining <- combined[dist_pair_idx, ]
  no_weak_idx <- grepl(pattern="ref_(G|C)", x=rownames(remaining))
  remaining <- remaining[no_weak_idx, ]
  
  print(head(table(position_table[["dist"]])))
  sequentials <- position_table[["dist"]] <= maximum_separation
  message("There are ", sum(sequentials), " candidate regions.")

  ## The following can tell me how many runs of each length occurred, that is not quite what I want.
  ## Now use run length encoding to find the set of sequential sequentials!
  rle_result <- rle(sequentials)
  rle_values <- rle_result[["values"]]
  ## The following line is equivalent to just leaving values alone:
  ## true_values <- rle_result[["values"]] == TRUE
  rle_lengths <- rle_result[["lengths"]]
  true_sequentials <- rle_lengths[rle_values]
  rle_idx <- cumsum(rle_lengths)[which(rle_values)]

  position_table[["last_sequential"]] <- 0
  count <- 0
  for (r in rle_idx) {
    count <- count + 1
    position_table[r, "last_sequential"] <- true_sequentials[count]
  }
  message("The maximum sequential set is: ", max(position_table[["last_sequential"]]), ".")

  wanted_idx <- position_table[["last_sequential"]] >= minimum
  wanted <- position_table[wanted_idx, c("chr", "pos")]
  return(wanted)
}

zymo22_sequentials <- sequential_variants(new_sets, conditions = "22", minimum=1, maximum_separation=2)
dim(zymo22_sequentials)
## 7 candidate regions for zymodeme 2.2 -- thus I am betting that the reference strain is a 2.2
zymo23_sequentials <- sequential_variants(new_sets, conditions = "23",
                                          minimum = 2, maximum_separation = 2)
dim(zymo23_sequentials)
## In contrast, there are lots (587) of interesting regions for 2.3!

8.1.2 Extract a promising region from the genome

The first 4 candidate regions from my set of remaining: * Chr Pos. Distance * LpaL13-15 238433 448 * LpaL13-18 142844 613 * LpaL13-29 830342 252 * LpaL13-33 1331507 843

Lets define a couple of terms: * Third: Each of the 4 above positions. * Second: Third - Distance * End: Third + PrimerLen * Start: Second - Primerlen

In each instance, these are the last positions, so we want to grab three things:

The entire region from End -> Start, this way we can have a quick sanity check.
Start -> Second.
(Third -> End) <- Reverse complemented

## * LpaL13-15 238433 448
first_candidate_chr <- genome[["LpaL13_15"]]
primer_length <- 22
amplicon_length <- 448
first_candidate_third <- 238433
first_candidate_second <- first_candidate_third - amplicon_length
first_candidate_start <- first_candidate_second - primer_length
first_candidate_end <- first_candidate_third + primer_length
first_candidate_region <- subseq(first_candidate_chr, first_candidate_start, first_candidate_end)
first_candidate_region
first_candidate_5p <- subseq(first_candidate_chr, first_candidate_start, first_candidate_second)
as.character(first_candidate_5p)
first_candidate_3p <- spgs::reverseComplement(subseq(first_candidate_chr, first_candidate_third, first_candidate_end))
first_candidate_3p


## * LpaL13-18 142844 613
second_candidate_chr <- genome[["LpaL13_18"]]
primer_length <- 22
amplicon_length <- 613
second_candidate_third <- 142844
second_candidate_second <- second_candidate_third - amplicon_length
second_candidate_start <- second_candidate_second - primer_length
second_candidate_end <- second_candidate_third + primer_length
second_candidate_region <- subseq(second_candidate_chr, second_candidate_start, second_candidate_end)
second_candidate_region
second_candidate_5p <- subseq(second_candidate_chr, second_candidate_start, second_candidate_second)
as.character(second_candidate_5p)
second_candidate_3p <- spgs::reverseComplement(subseq(second_candidate_chr, second_candidate_third, second_candidate_end))
second_candidate_3p


## * LpaL13-29 830342 252
third_candidate_chr <- genome[["LpaL13_29"]]
primer_length <- 22
amplicon_length <- 252
third_candidate_third <- 830342
third_candidate_second <- third_candidate_third - amplicon_length
third_candidate_start <- third_candidate_second - primer_length
third_candidate_end <- third_candidate_third + primer_length
third_candidate_region <- subseq(third_candidate_chr, third_candidate_start, third_candidate_end)
third_candidate_region
third_candidate_5p <- subseq(third_candidate_chr, third_candidate_start, third_candidate_second)
as.character(third_candidate_5p)
third_candidate_3p <- spgs::reverseComplement(subseq(third_candidate_chr, third_candidate_third, third_candidate_end))
third_candidate_3p
## You are a garbage polypyrimidine tract.
## Which is actually interesting if the mutations mess it up.


## * LpaL13-33 1331507 843
fourth_candidate_chr <- genome[["LpaL13_33"]]
primer_length <- 22
amplicon_length <- 843
fourth_candidate_third <- 1331507
fourth_candidate_second <- fourth_candidate_third - amplicon_length
fourth_candidate_start <- fourth_candidate_second - primer_length
fourth_candidate_end <- fourth_candidate_third + primer_length
fourth_candidate_region <- subseq(fourth_candidate_chr, fourth_candidate_start, fourth_candidate_end)
fourth_candidate_region
fourth_candidate_5p <- subseq(fourth_candidate_chr, fourth_candidate_start, fourth_candidate_second)
as.character(fourth_candidate_5p)
fourth_candidate_3p <- spgs::reverseComplement(subseq(fourth_candidate_chr, fourth_candidate_third, fourth_candidate_end))
fourth_candidate_3p

8.2 Go hunting for Sanger sequencing regions

I made a fun little function which should find regions which have lots of variants associated with a given experimental factor.

pheno <- subset_expt(lp_expt, subset = "condition=='z2.2'|condition=='z2.3'")
pheno <- subset_expt(pheno, subset = "!is.na(pData(pheno)[['bcftable']])")
pheno_snps <- sm(count_expt_snps(pheno, annot_column = "bcftable"))

fun_stuff <- snp_density_primers(pheno_snps,
                                 bsgenome="BSGenome.Leishmania.panamensis.MHOMCOL81L13.v53",
                                 gff="reference/TriTrypDB-53_LpanamensisMHOMCOL81L13.gff")
drop_scaffolds <- grepl(x = rownames(fun_stuff$favorites), pattern = "SCAF")
favorite_primer_regions <- fun_stuff[["favorites"]][!drop_scaffolds, ]
favorite_primer_regions[["bin"]] <- rownames(favorite_primer_regions)
library(dplyr)
favorite_primer_regions <- favorite_primer_regions %>%
  relocate(bin)

8.3 Combine this table with 2.2/2.3 genes

Here is my note from our meeting:

Cross reference primers to DE genes of 2.2/2.3 and/or resistance/suscpetible, add a column to the primer spreadsheet with the DE genes (in retrospect I am guessing this actually means to put the logFC as a column.

One nice thing, I did a semantic removal on the lp_expt, so the set of logFC/pvalues should not have any of the offending types; thus I should be able to automagically get rid of them in the merge.

logfc <- zy_table[["data"]][["z23_vs_z22"]]
logfc_columns <- logfc[, c("deseq_logfc", "deseq_adjp")]
colnames(logfc_columns) <- c("z23_logfc", "z23_adjp")
new_table <- merge(favorite_primer_regions, logfc_columns,
                   by.x = "closest_gene_before_id", by.y = "row.names")
sus <- sus_table[["data"]][["sensitive_vs_resistant"]]
sus_columns <- sus[, c("deseq_logfc", "deseq_adjp")]
colnames(sus_columns) <- c("sus_logfc", "sus_adjp")
new_table <- merge(new_table, sus_columns,
                   by.x = "closest_gene_before_id", by.y = "row.names") %>%
  relocate(bin)
written <- write_xlsx(data=new_table,
                      excel="excel/favorite_primers_xref_zy_sus.

## Error: <text>:13:29: unexpected INCOMPLETE_STRING
## 12: written <- write_xlsx(data=new_table,
## 13:                       excel="excel/favorite_primers_xref_zy_sus.
##                                 ^

8.4 Make a heatmap describing the clustering of variants

We can cross reference the variants against the zymodeme status and plot a heatmap of the results and hopefully see how they separate.

snp_genes <- sm(snps_vs_genes(lp_expt, new_sets, expt_name_col = "chromosome"))
new_zymo_norm <- normalize_expt(new_snps, filter = TRUE, convert = "cpm", norm = "quant", transform = TRUE)

## Removing 0 low-count genes (568413 remaining).

## transform_counts: Found 18767635 values equal to 0, adding 1 to the matrix.

new_zymo_norm <- set_expt_conditions(new_zymo_norm, fact = "phenotypiccharacteristics")

zymo_heat <- plot_disheat(new_zymo_norm)
zymo_heat[["plot"]]

8.4.1 Annotated heatmap of variants

Now let us try to make a heatmap which includes some of the annotation data.

des <- both_norm[["design"]]
undef_idx <- is.na(des[["strain"]])
des[undef_idx, "strain"] <- "unknown"

##hmcols <- colorRampPalette(c("yellow","black","darkblue"))(256)
correlations <- hpgl_cor(exprs(both_norm))

zymo_missing_idx <- is.na(des[["phenotypiccharacteristics"]])
des[["phenotypiccharacteristics"]] <- as.character(des[["phenotypiccharacteristics"]])
des[["clinicalcategorical"]] <- as.character(des[["clinicalcategorical"]])
des[zymo_missing_idx, "phenotypiccharacteristics"] <- "unknown"
mydendro <- list(
  "clustfun" = hclust,
  "lwd" = 2.0)
col_data <- as.data.frame(des[, c("phenotypiccharacteristics", "clinicalcategorical")])

unknown_clinical <- is.na(col_data[["clinicalcategorical"]])
row_data <- as.data.frame(des[, c("strain")])
colnames(col_data) <- c("zymodeme", "outcome")
col_data[unknown_clinical, "outcome"] <- "undefined"

colnames(row_data) <- c("strain")
myannot <- list(
  "Col" = list("data" = col_data),
  "Row" = list("data" = row_data))
myclust <- list("cuth" = 1.0,
                "col" = BrewerClusterCol)
mylabs <- list(
  "Row" = list("nrow" = 4),
  "Col" = list("nrow" = 4))
hmcols <- colorRampPalette(c("darkblue", "beige"))(240)
map1 <- annHeatmap2(
  correlations,
  dendrogram = mydendro,
  annotation = myannot,
  cluster = myclust,
  labels = mylabs,
  ## The following controls if the picture is symmetric
  scale = "none",
  col = hmcols)

## Warning in breakColors(breaks, col): more colors than classes: ignoring 29 last
## colors

pp(file = "images/dendro_heatmap.png", image = map1, height = 20, width = 20)

## annotated Heatmap
## 
## Rows: 'dendrogram' with 2 branches and 99 members total, at height 6.095 
##   11  annotation variable(s)
## Cols: 'dendrogram' with 2 branches and 99 members total, at height 6.095 
##   12  annotation variable(s)

Print the larger heatmap so that all the labels appear. Keep in mind that as we get more samples, this image needs to continue getting bigger.

big heatmap

xref_prop <- table(pheno_snps[["conditions"]])

## Error in eval(quote(list(...)), env): object 'pheno_snps' not found

pheno_snps$conditions

## Error in eval(expr, envir, enclos): object 'pheno_snps' not found

idx_tbl <- exprs(pheno_snps) > 5

## Error in h(simpleError(msg, call)): error in evaluating the argument 'object' in selecting a method for function 'exprs': object 'pheno_snps' not found

new_tbl <- data.frame(row.names = rownames(exprs(pheno_snps)))

## Error in h(simpleError(msg, call)): error in evaluating the argument 'x' in selecting a method for function 'rownames': error in evaluating the argument 'object' in selecting a method for function 'exprs': object 'pheno_snps' not found

for (n in names(xref_prop)) {
  new_tbl[[n]] <- 0
  idx_cols <- which(pheno_snps[["conditions"]] == n)
  prop_col <- rowSums(idx_tbl[, idx_cols]) / xref_prop[n]
  new_tbl[n] <- prop_col
}

## Error in eval(expr, envir, enclos): object 'xref_prop' not found

keepers <- grepl(x = rownames(new_tbl), pattern = "LpaL13")

## Error in h(simpleError(msg, call)): error in evaluating the argument 'x' in selecting a method for function 'grepl': error in evaluating the argument 'x' in selecting a method for function 'rownames': object 'new_tbl' not found

new_tbl <- new_tbl[keepers, ]

## Error in eval(expr, envir, enclos): object 'new_tbl' not found

new_tbl[["strong22"]] <- 1.001 - new_tbl[["z2.2"]]

## Error in eval(expr, envir, enclos): object 'new_tbl' not found

new_tbl[["strong23"]] <- 1.001 - new_tbl[["z2.3"]]

## Error in eval(expr, envir, enclos): object 'new_tbl' not found

s22_na <- new_tbl[["strong22"]] > 1

## Error in eval(expr, envir, enclos): object 'new_tbl' not found

new_tbl[s22_na, "strong22"] <- 1

## Error in new_tbl[s22_na, "strong22"] <- 1: object 'new_tbl' not found

s23_na <- new_tbl[["strong23"]] > 1

## Error in eval(expr, envir, enclos): object 'new_tbl' not found

new_tbl[s23_na, "strong23"] <- 1

## Error in new_tbl[s23_na, "strong23"] <- 1: object 'new_tbl' not found

new_tbl[["SNP"]] <- rownames(new_tbl)

## Error in h(simpleError(msg, call)): error in evaluating the argument 'x' in selecting a method for function 'rownames': object 'new_tbl' not found

new_tbl[["Chromosome"]] <- gsub(x = new_tbl[["SNP"]], pattern = "chr_(.*)_pos_.*", replacement = "\\1")

## Error in h(simpleError(msg, call)): error in evaluating the argument 'x' in selecting a method for function 'gsub': object 'new_tbl' not found

new_tbl[["Position"]] <- gsub(x = new_tbl[["SNP"]], pattern = ".*_pos_(\\d+)_.*", replacement = "\\1")

## Error in h(simpleError(msg, call)): error in evaluating the argument 'x' in selecting a method for function 'gsub': object 'new_tbl' not found

new_tbl <- new_tbl[, c("SNP", "Chromosome", "Position", "strong22", "strong23")]

## Error in eval(expr, envir, enclos): object 'new_tbl' not found

library(CMplot)

## Much appreciate for using CMplot.

## Full description, Bug report, Suggestion and the latest codes:

## https://github.com/YinLiLin/CMplot

simplify <- new_tbl

## Error in eval(expr, envir, enclos): object 'new_tbl' not found

simplify[["strong22"]] <- NULL

## Error in simplify[["strong22"]] <- NULL: object 'simplify' not found

CMplot(simplify, bin.size = 100000)

## Error in is.data.frame(x): object 'simplify' not found

CMplot(new_tbl, plot.type="m", multracks=TRUE, threshold = c(0.01, 0.05),
       threshold.lwd=c(1,1), threshold.col=c("black","grey"),
       amplify=TRUE, bin.size=10000,
       chr.den.col=c("darkgreen", "yellow", "red"),
       signal.col=c("red", "green", "blue"),
       signal.cex=1, file="jpg", memo="", dpi=300, file.output=TRUE, verbose=TRUE)

## Error in is.data.frame(x): object 'new_tbl' not found

$Circular Manhattan$ Rectangular Manhattan

8.5 Try out MatrixEQTL

This tool looks a little opaque, but provides sample data with things that make sense to me and should be pretty easy to recapitulate in our data.

covariates.txt: Columns are samples, rows are things from pData – the most likely ones of interest for our data would be zymodeme, sensitivity
geneloc.txt: columns are ‘geneid’, ‘chr’, ‘left’, ‘right’. I guess I can assume left and right are start/stop; in which case this is trivially acquirable from fData.
ge.txt: This appears to be a log(rpkm/cpm) table with rows as genes and columns as samples
snpsloc.txt: columns are ‘snpid’, ‘chr’, ‘pos’
snps.txt: columns are samples, rows are the ids from snsploc, values a 0,1,2. I assume 0 is identical and 1..12 are the various A->TGC T->AGC C->AGT G->ACT

## For this, let us use the 'new_snps' data structure.
## Caveat here: these need to be coerced to numbers.
my_covariates <- pData(new_snps)[, c("phenotypiccharacteristics", "clinicalcategorical")]
for (col in colnames(my_covariates)) {
  my_covariates[[col]] <- as.numeric(as.factor(my_covariates[[col]]))
}
my_covariates <- t(my_covariates)

my_geneloc <- fData(lp_expt)[, c("gid", "chromosome", "start", "end")]
colnames(my_geneloc) <- c("geneid", "chr", "left", "right")

my_ge <- exprs(normalize_expt(lp_expt, transform = "log2", filter = TRUE, convert = "cpm"))
used_samples <- tolower(colnames(my_ge)) %in% colnames(exprs(new_snps))
my_ge <- my_ge[, used_samples]

my_snpsloc <- data.frame(rownames = rownames(exprs(new_snps)))
## Oh, caveat here: Because of the way I stored the data,
## I could have duplicate rows which presumably will make matrixEQTL sad
my_snpsloc[["chr"]] <- gsub(pattern = "^chr_(.+)_pos(.+)_ref_.*$", replacement = "\\1",
                            x = rownames(my_snpsloc))
my_snpsloc[["pos"]] <- gsub(pattern = "^chr_(.+)_pos(.+)_ref_.*$", replacement = "\\2",
                            x = rownames(my_snpsloc))
test <- duplicated(my_snpsloc)
## Each duplicated row would be another variant at that position;
## so in theory we would do a rle to number them I am guessing
## However, I do not have different variants so I think I can ignore this for the moment
## but will need to make my matrix either 0 or 1.
if (sum(test) > 0) {
  message("There are: ", sum(duplicated), " duplicated entries.")
  keep_idx <- ! test
  my_snpsloc <- my_snpsloc[keep_idx, ]
}

my_snps <- exprs(new_snps)
one_idx <- my_snps > 0
my_snps[one_idx] <- 1

## Ok, at this point I think I have all the pieces which this method wants...
## Oh, no I guess not; it actually wants the data as a set of filenames...
library(MatrixEQTL)
write.table(my_snps, "eqtl/snps.tsv", na = "NA", col.names = TRUE, row.names = TRUE, sep = "\t", quote = TRUE)
## readr::write_tsv(my_snps, "eqtl/snps.tsv", )
write.table(my_snpsloc, "eqtl/snpsloc.tsv", na = "NA", col.names = TRUE, row.names = TRUE, sep = "\t", quote = TRUE)
## readr::write_tsv(my_snpsloc, "eqtl/snpsloc.tsv")
write.table(as.data.frame(my_ge), "eqtl/ge.tsv", na = "NA", col.names = TRUE, row.names = TRUE, sep = "\t", quote = TRUE)
## readr::write_tsv(as.data.frame(my_ge), "eqtl/ge.tsv")
write.table(as.data.frame(my_geneloc), "eqtl/geneloc.tsv", na = "NA", col.names = TRUE, row.names = TRUE, sep = "\t", quote = TRUE)
## readr::write_tsv(as.data.frame(my_geneloc), "eqtl/geneloc.tsv")
write.table(as.data.frame(my_covariates), "eqtl/covariates.tsv", na = "NA", col.names = TRUE, row.names = TRUE, sep = "\t", quote = TRUE)
## readr::write_tsv(as.data.frame(my_covariates), "eqtl/covariates.tsv")

useModel = modelLINEAR # modelANOVA, modelLINEAR, or modelLINEAR_CROSS

# Genotype file name
SNP_file_name = "eqtl/snps.tsv"
snps_location_file_name = "eqtl/snpsloc.tsv"
expression_file_name = "eqtl/ge.tsv"
gene_location_file_name = "eqtl/geneloc.tsv"
covariates_file_name = "eqtl/covariates.tsv"
# Output file name
output_file_name_cis = tempfile()
output_file_name_tra = tempfile()
# Only associations significant at this level will be saved
pvOutputThreshold_cis = 0.1
pvOutputThreshold_tra = 0.1
# Error covariance matrix
# Set to numeric() for identity.
errorCovariance = numeric()
# errorCovariance = read.table("Sample_Data/errorCovariance.txt");
# Distance for local gene-SNP pairs
cisDist = 1e6
## Load genotype data
snps = SlicedData$new()
snps$fileDelimiter = "\t"      # the TAB character
snps$fileOmitCharacters = "NA" # denote missing values;
snps$fileSkipRows = 1          # one row of column labels
snps$fileSkipColumns = 1       # one column of row labels
snps$fileSliceSize = 2000      # read file in slices of 2,000 rows
snps$LoadFile(SNP_file_name)
## Load gene expression data
gene = SlicedData$new()
gene$fileDelimiter = "\t"      # the TAB character
gene$fileOmitCharacters = "NA" # denote missing values;
gene$fileSkipRows = 1          # one row of column labels
gene$fileSkipColumns = 1       # one column of row labels
gene$fileSliceSize = 2000      # read file in slices of 2,000 rows
gene$LoadFile(expression_file_name)
## Load covariates
cvrt = SlicedData$new()
cvrt$fileDelimiter = "\t"      # the TAB character
cvrt$fileOmitCharacters = "NA" # denote missing values;
cvrt$fileSkipRows = 1          # one row of column labels
cvrt$fileSkipColumns = 1       # one column of row labels
if(length(covariates_file_name) > 0) {
  cvrt$LoadFile(covariates_file_name)
}
## Run the analysis
snpspos = read.table(snps_location_file_name, header = TRUE, stringsAsFactors = FALSE)
genepos = read.table(gene_location_file_name, header = TRUE, stringsAsFactors = FALSE)

me = Matrix_eQTL_main(
    snps = snps,
    gene = gene,
    cvrt = cvrt,
    output_file_name = output_file_name_tra,
    pvOutputThreshold = pvOutputThreshold_tra,
    useModel = useModel,
    errorCovariance = errorCovariance,
    verbose = TRUE,
    output_file_name.cis = output_file_name_cis,
    pvOutputThreshold.cis = pvOutputThreshold_cis,
    snpspos = snpspos,
    genepos = genepos,
    cisDist = cisDist,
    pvalue.hist = "qqplot",
    min.pv.by.genesnp = FALSE,
    noFDRsaveMemory = FALSE);

if (!isTRUE(get0("skip_load"))) {
  pander::pander(sessionInfo())
  message(paste0("This is hpgltools commit: ", get_git_commit()))
  message(paste0("Saving to ", savefile))
  tmp <- sm(saveme(filename = savefile))
}

## If you wish to reproduce this exact build of hpgltools, invoke the following:

## > git clone http://github.com/abelew/hpgltools.git

## > git reset 907cf8a97fc8442486011d20ba826130f018bdbb

## This is hpgltools commit: Sat Aug 21 11:09:20 2021 -0400: 907cf8a97fc8442486011d20ba826130f018bdbb

## Saving to tmrc2_02sample_estimation_v202108.rda.xz

tmp <- loadme(filename = savefile)

---
title: "TMRC2 Comprehensive Data Analysis: 202108"
author: "atb abelew@gmail.com"
date: "`r Sys.Date()`"
output:
 html_document:
  code_download: true
  code_folding: show
  fig_caption: true
  fig_height: 7
  fig_width: 7
  highlight: default
  keep_md: false
  mode: selfcontained
  number_sections: true
  self_contained: true
  theme: readable
  toc: true
  toc_float:
   collapsed: false
   smooth_scroll: false
---

<style>
  body .main-container {
    max-width: 1600px;
  }
</style>

```{r options, include = FALSE}
library(hpgltools)
tt <- sm(devtools::load_all("~/hpgltools"))
knitr::opts_knit$set(progress = TRUE,
                     verbose = TRUE,
                     width = 90,
                     echo = TRUE)
knitr::opts_chunk$set(error = TRUE,
                      fig.width = 8,
                      fig.height = 8,
                      dpi = 96)
old_options <- options(digits = 4,
                       stringsAsFactors = FALSE,
                       knitr.duplicate.label = "allow")
ggplot2::theme_set(ggplot2::theme_bw(base_size = 12))
ver <- "202108"
rundate <- format(Sys.Date(), format = "%Y%m%d")

## tmp <- try(sm(loadme(filename = gsub(pattern = "\\.Rmd", replace = "\\.rda\\.xz", x = previous_file))))
rmd_file <- glue::glue("tmrc2_02sample_estimation_v{ver}.Rmd")
savefile <- gsub(pattern = "\\.Rmd", replace = "\\.rda\\.xz", x = rmd_file)

library(Heatplus)
```

```{r current_samplesheet}
sample_sheet <- glue::glue("sample_sheets/tmrc2_samples_20210817.xlsx")
```

# Introduction

This document is intended to provide a general overview of the TMRC2 samples
which have thus far been sequenced.  In some cases, this includes only those
samples starting in 2019; in other instances I am including our previous
(2015-2016) samples.

In all cases the processing performed was:

1.  Default trimming was performed.
2.  Hisat2 was used to map the remaining reads against the Leishmania
    panamensis genome revision 36.
3.  The alignments from hisat2 were used to count reads/gene against the
    revision 36 annotations with htseq.
4.  These alignments were also passed to the pileup functionality of samtools
    and the vcf/bcf utilities in order to make a matrix of all observed
    differences between each sample with respect to the reference.

The analyses in this document use the matrices of counts/gene from #3 and
variants/position from #4 in order to provide some images and metrics describing
the samples we have sequenced so far.

# Annotations

Everything which follows depends on the Existing TriTrypDB annotations revision
46, circa 2019.  The following block loads a database of these annotations and
turns it into a matrix where the rows are genes and columns are all the
annotation types provided by TriTrypDB.

The same database was used to create a matrix of orthologous genes between
L.panamensis and all of the other species in the TriTrypDB.

```{r annot}
tt <- sm(library(EuPathDB))
tt <- sm(library(org.Lpanamensis.MHOMCOL81L13.v46.eg.db))
pan_db <- org.Lpanamensis.MHOMCOL81L13.v46.eg.db
all_fields <- columns(pan_db)

all_lp_annot <- sm(load_orgdb_annotations(
    pan_db,
    keytype = "gid",
    fields = c("annot_gene_entrez_id", "annot_gene_name",
               "annot_strand", "annot_chromosome", "annot_cds_length",
               "annot_gene_product")))$genes

lp_go <- sm(load_orgdb_go(pan_db))
lp_lengths <- all_lp_annot[, c("gid", "annot_cds_length")]
colnames(lp_lengths)  <- c("ID", "length")
all_lp_annot[["annot_gene_product"]] <- tolower(all_lp_annot[["annot_gene_product"]])
orthos <- sm(EuPathDB::extract_eupath_orthologs(db = pan_db))

hisat_annot <- all_lp_annot
## rownames(hisat_annot) <- paste0("exon_", rownames(hisat_annot), ".E1")
```

# Load a genome

```{r genome}
meta <- EuPathDB::download_eupath_metadata(webservice="tritrypdb")
lp_entry <- EuPathDB::get_eupath_entry(species="Leishmania panamensis", metadata=meta)
lp_entry
## testing_panamensis <- EuPathDB::make_eupath_bsgenome(entry=lp_entry)
library(as.character(testing_panamensis), character.only=TRUE)
genome <- get0(as.character(testing_panamensis))
```

# TODO:

Resequence samples: TMRC20002, TMRC20006, TMRC20004 (maybe TMRC20008 and TMRC20029)

# Generate Expressionsets and Sample Estimation

The process of sample estimation takes two primary inputs:

1.  The sample sheet, which contains all the metadata we currently have on hand,
    including filenames for the outputs of #3 and #4 above.
2.  The gene annotations.

An expressionset is a data structure used in R to examine RNASeq data.  It
is comprised of annotations, metadata, and expression data.  In the case of our
processing pipeline, the location of the expression data is provided by the
filenames in the metadata.

The first lines of the following block create the Expressionset.  All of the
following lines perform various normalizations and generate plots from it.

## Notes

The following samples are much lower coverage:

* TMRC20002
* TMRC20006
* TMRC20007
* TMRC20008

20210610: I made some manual changes to the sample sheet which I
downloaded, filling in some zymodeme with 'unknown'

## TODO:

1.  Do the multi-gene family removal right here instead of way down at the bottom
2.  Add zymodeme snps to the annotation later.
3.  Start phylogenetic analysis of variant table.

```{r new_samples_hisat}
sanitize_columns <- c("passagenumber", "clinicalresponse", "clinicalcategorical",
                      "zymodemecategorical", "phenotypiccharacteristics")
lp_expt <- sm(create_expt(sample_sheet,
                          gene_info = hisat_annot,
                          id_column = "hpglidentifier",
                          file_column = "lpanamensisv36hisatfile")) %>%
  set_expt_conditions(fact = "zymodemecategorical") %>%
  subset_expt(nonzero = 8550) %>%
  subset_expt(coverage = 5000000) %>%
  semantic_expt_filter(semantic = c("amastin", "gp63", "leishmanolysin"),
                       semantic_column = "annot_gene_product") %>%
  sanitize_expt_metadata(columns = sanitize_columns) %>%
  set_expt_factors(columns = sanitize_columns, class = "factor")

libsizes <- plot_libsize(lp_expt)
pp(file = "images/lp_expt_libsizes.png", image = libsizes$plot, width = 14, height = 9)
## I think samples 7,10 should be removed at minimum, probably also 9,11
nonzero <- plot_nonzero(lp_expt)
pp(file = "images/lp_nonzero.png", image = nonzero$plot, width = 9, height = 9)

lp_box <- plot_boxplot(lp_expt)
pp(file = "images/lp_expt_boxplot.png", image = lp_box, width = 12, height = 9)

filter_plot <- plot_libsize_prepost(lp_expt)
filter_plot$lowgene_plot
filter_plot$count_plot
```

## Distribution Visualization

Najib's favorite plots are of course the PCA/TNSE.  These are nice to look at in
order to get a sense of the relationships between samples.  They also provide a
good opportunity to see what happens when one applies different normalizations,
surrogate analyses, filters, etc.  In addition, one may set different
experimental factors as the primary 'condition' (usually the color of plots) and
surrogate 'batches'.

## By Susceptilibity

Column 'Q' in the sample sheet, make a categorical version of it with these parameters:

* 0 <= x <= 35 is resistant
* 36 <= x <= 48 is ambiguous
* 49 <= x is sensitive

```{r susceptibility}
starting <- as.numeric(pData(lp_expt)[["susceptibilityinfectionreduction32ugmlsbvhistoricaldata"]])
sus_categorical <- starting
na_idx <- is.na(starting)
sus_categorical[na_idx] <- "unknown"

resist_idx <- starting <= 0.35
sus_categorical[resist_idx] <- "resistant"
indeterminant_idx <- starting >= 0.36 & starting <= 0.48
sus_categorical[indeterminant_idx] <- "ambiguous"
susceptible_idx <- starting >= 0.49
sus_categorical[susceptible_idx] <- "sensitive"

pData(lp_expt$expressionset)[["sus_category"]] <- sus_categorical
```

```{r pre_questions}
clinical_colors <- list(
    "z2.3" = "#874400",
    "z2.2" = "#df7000",
    "unknown" = "#cbcbcb",
    "null" = "#000000")
clinical_samples <- lp_expt %>%
  set_expt_batches(fact = sus_categorical) %>%
  set_expt_colors(clinical_colors)

clinical_norm <- sm(normalize_expt(clinical_samples, norm = "quant", transform = "log2",
                                   convert = "cpm", batch = FALSE, filter = TRUE))
zymo_pca <- plot_pca(clinical_norm, plot_title = "PCA of parasite expression values",
                     plot_labels = FALSE)
pp(file = "images/zymo_pca_sus_shape.png", image = zymo_pca$plot)

zymo_3dpca <- plot_3d_pca(zymo_pca)
zymo_3dpca$plot

clinical_n <- sm(normalize_expt(clinical_samples, transform = "log2",
                                convert = "cpm", batch = FALSE, filter = TRUE))
zymo_tsne <- plot_tsne(clinical_n, plot_title = "TSNE of parasite expression values")
zymo_tsne$plot

clinical_nb <- normalize_expt(clinical_samples, convert = "cpm", transform = "log2",
                         filter = TRUE, batch = "svaseq")
clinical_nb_pca <- plot_pca(clinical_nb, plot_title = "PCA of parasite expression values",
                            plot_labels = FALSE)
pp(file = "images/clinical_nb_pca_sus_shape.png", image = clinical_nb_pca$plot)

clinical_nb_tsne <- plot_tsne(clinical_nb, plot_title = "TSNE of parasite expression values")
clinical_nb_tsne$plot

corheat <- plot_corheat(clinical_norm, plot_title = "Correlation heatmap of parasite
                 expression values
")
corheat$plot

plot_sm(clinical_norm)$plot
```

## By Cure/Fail status

```{r cf_status}
cf_colors <- list(
    "cure" = "#006f00",
    "fail" = "#9dffa0",
    "unknown" = "#cbcbcb",
    "notapplicable" = "#000000")
cf_expt <- set_expt_conditions(lp_expt, fact = "clinicalcategorical") %>%
  set_expt_batches(fact = sus_categorical) %>%
  set_expt_colors(cf_colors)

cf_norm <- normalize_expt(cf_expt, convert = "cpm", transform = "log2",
                          norm = "quant", filter = TRUE)
start_cf <- plot_pca(cf_norm, plot_title = "PCA of parasite expression values",
                     plot_labels = FALSE)
pp(file = "images/cf_sus_shape.png", image = start_cf$plot)

cf_nb <- normalize_expt(cf_expt, convert = "cpm", transform = "log2",
                        norm = "quant", filter = TRUE, batch = "svaseq")
cf_nb_pca <- plot_pca(cf_nb, plot_title = "PCA of parasite expression values",
                      plot_labels = FALSE)
pp(file = "images/cf_sus_share_nb.png", image = cf_nb_pca$plot)

cf_norm <- normalize_expt(cf_expt, transform = "log2", convert = "cpm",
                          filter = TRUE, norm = "quant")

test <- pca_information(cf_norm,
                        expt_factors = c("clinicalcategorical", "zymodemecategorical",
                                         "pathogenstrain", "passagenumber"),
                        num_components = 6, plot_pcas = TRUE)
test$anova_p
test$cor_heatmap
```

```{r susceptibility_pca}
sus_colors <- list(
    "resistant" = "#8563a7",
    "sensitive" = "#8d0000",
    "ambiguous" = "#cbcbcb",
    "unknown" = "#000000")
sus_expt <- set_expt_conditions(lp_expt, fact = "sus_category") %>%
  set_expt_batches(fact = "zymodemecategorical")

test <- set_expt_colors(sus_expt, sus_colors)


sus_norm <- normalize_expt(sus_expt, transform = "log2", convert = "cpm",
                           norm = "quant", filter = TRUE)
sus_pca <- plot_pca(sus_norm, plot_title = "PCA of parasite expression values",
                    plot_labels = FALSE)
pp(file = "images/sus_norm_pca.png", image = sus_pca[["plot"]])

sus_nb <- normalize_expt(sus_expt, transform = "log2", convert = "cpm",
                         batch = "svaseq", filter = TRUE)
sus_nb_pca <- plot_pca(sus_nb, plot_title = "PCA of parasite expression values",
                       plot_labels = FALSE)
pp(file = "images/sus_nb_pca.png", image = sus_nb_pca[["plot"]])
```

At this time, we do not have very many samples, so the set of metrics/plots is
fairly limited.  There is really only one factor in the metadata which we can
use for performing differential expression analyses, the 'zymodeme'.

# Zymodeme analyses

The following sections perform a series of analyses which seek to elucidate
differences between the zymodemes 2.2 and 2.3 either through differential
expression or variant profiles.

## Differential expression

### With respect to zymodeme attribution

TODO: Do this with and without sva and compare the results.

```{r zymo_de, fig.show = "hide"}
zy_expt <- subset_expt(lp_expt, subset = "condition=='z2.2'|condition=='z2.3'")
zy_norm <- normalize_expt(zy_expt, filter = TRUE, convert = "cpm", norm = "quant")
zy_de_nobatch <- sm(all_pairwise(zy_expt, filter = TRUE, model_batch = "svaseq"))
zy_de <- sm(all_pairwise(zy_expt, filter = TRUE, model_batch = "svaseq"))
zy_table <- sm(combine_de_tables(zy_de, excel = glue::glue("excel/zy_tables-v{ver}.xlsx")))
zy_sig <- sm(extract_significant_genes(zy_table, excel = glue::glue("excel/zy_sig-v{ver}.xlsx")))
```

### Images of zymodeme DE

```{r zymod_de_pictures}
pp(file = "images/zymo_ma.png", image = zy_table[["plots"]][["z23_vs_z22"]][["deseq_ma_plots"]][["plot"]])
```

## With respect to cure/failure

In contrast, we can search for genes which are differentially
expressed with respect to cure/failure status.

```{r curefail_de, fig.show = "hide"}
cf_de <- sm(all_pairwise(cf_expt, filter = TRUE, model_batch = "svaseq"))
cf_table <- sm(combine_de_tables(cf_de, excel = glue::glue("excel/cf_tables-v{ver}.xlsx")))
cf_sig <- sm(extract_significant_genes(cf_table, excel = glue::glue("excel/cf_sig-v{ver}.xlsx")))
```

## With respect to susceptibility

Finally, we can use our category of susceptibility and look for genes
which change from sensitive to resistant.  Keep in mind, though, that
for the moment we have a lot of ambiguous and unknown strains.

```{r curefail_de, fig.show = "hide"}
sus_de <- sm(all_pairwise(sus_expt, filter = TRUE, model_batch = "svaseq"))
sus_table <- sm(combine_de_tables(sus_de, excel = glue::glue("excel/sus_tables-v{ver}.xlsx")))
sus_sig <- sm(extract_significant_genes(sus_table, excel = glue::glue("excel/sus_sig-v{ver}.xlsx")))
```

```{r zymod_de_pictures}
knitr::kable(head(sus_sig$deseq$ups$sensitive_vs_resistant, n = 20))

knitr::kable(head(sus_sig$deseq$downs$sensitive_vs_resistant, n = 20))

sus_ma <- sus_table[["plots"]][["sensitive_vs_resistant"]][["deseq_ma_plots"]][["plot"]]
pp(file = "images/sus_ma.png", image = sus_ma)

## test <- ggplt(sus_ma)
```

## Ontology searches

Now let us look for ontology categories which are increased in the 2.3
samples followed by the 2.2 samples.

```{r go, sig.show = "hide"}
## Gene categories more represented in the 2.3 group.
zy_go_up <- sm(simple_goseq(sig_genes = zy_sig[["deseq"]][["ups"]][[1]],
                            go_db = lp_go, length_db = lp_lengths))

## Gene categories more represented in the 2.2 group.
zy_go_down <- sm(simple_goseq(sig_genes = zy_sig[["deseq"]][["downs"]][[1]],
                              go_db = lp_go, length_db = lp_lengths))
```

### A couple plots from the differential expression

#### Number of genes in agreement among DE methods, 2.3 more than 2.2

In the function 'combined_de_tables()' above, one of the tasks
performed is to look at the agreement among DESeq2, limma, and edgeR.
The following show a couple of these for the set of genes observed
with a fold-change >= |2| and adjusted p-value <= 0.05.

```{r de_plots}
zy_table[["venns"]][[1]][["p_lfc1"]][["up_noweight"]]
```

#### Number of genes in agreement among DE methods, 2.2 more than 2.3

```{r de_plots}
zy_table[["venns"]][[1]][["p_lfc1"]][["down_noweight"]]
```

#### goseq ontology plots of groups of genes, 2.3 more than 2.2

```{r goseq_up}
zy_go_up$pvalue_plots$bpp_plot_over
```

#### goseq ontology plots of groups of genes, 2.2 more than 2.3

```{r goseq_down}
zy_go_down$pvalue_plots$bpp_plot_over
```

## Look for agreement between sensitivity and zymodemes

Remind myself, the data structures are (zy|sus)_(de|table|sig).

```{r sensitive_vs_zymo}
zy_df <- zy_table[["data"]][["z23_vs_z22"]]
sus_df <- sus_table[["data"]][["sensitive_vs_resistant"]]

both_df <- merge(zy_df, sus_df, by = "row.names")
plot_df <- both_df[, c("deseq_logfc.x", "deseq_logfc.y")]
rownames(plot_df) <- both_df[["Row.names"]]
colnames(plot_df) <- c("z23_vs_z22", "sensitive_vs_resistant")

compare <- plot_linear_scatter(plot_df)
pp(file = "images/compare_sus_zy.png", image = compare$scatter)
compare$cor
```

## Zymodeme enzyme gene IDs

Najib read me an email listing off the gene names associated with the zymodeme
classification.  I took those names and cross referenced them against the
Leishmania panamensis gene annotations and found the following:

They are:

1. ALAT: LPAL13_120010900 -- alanine aminotransferase
2. ASAT: LPAL13_340013000 -- aspartate aminotransferase
3. G6PD: LPAL13_000054100 -- glucase-6-phosphate 1-dehydrogenase
4. NH: LPAL13_14006100, LPAL13_180018500 -- inosine-guanine nucleoside hydrolase
5. MPI: LPAL13_320022300 (maybe) -- mannose phosphate isomerase (I chose phosphomannose isomerase)

Given these 6 gene IDs (NH has two gene IDs associated with it), I can do some
looking for specific differences among the various samples.

### Expression levels of zymodeme genes

The following creates a colorspace (red to green) heatmap showing the observed
expression of these genes in every sample.

```{r zymodemes}
my_genes <- c("LPAL13_120010900", "LPAL13_340013000", "LPAL13_000054100",
              "LPAL13_140006100", "LPAL13_180018500", "LPAL13_320022300",
              "other")
my_names <- c("ALAT", "ASAT", "G6PD", "NHv1", "NHv2", "MPI", "other")

zymo_expt <- exclude_genes_expt(zy_norm, ids = my_genes, method = "keep")
zymo_heatmap <- plot_sample_heatmap(zymo_expt, row_label = my_names)
zymo_heatmap
```

## Empirically observed Zymodeme genes from differential expression analysis

In contrast, the following plots take the set of genes which are shared among
all differential expression methods (|lfc| >= 1.0 and adjp <= 0.05) and use them
to make categories of genes which are increased in 2.3 or 2.2.

```{r zymodeme_genes_empirical}
shared_zymo <- intersect_significant(zy_table)
up_shared <- shared_zymo[["ups"]][[1]][["data"]][["all"]]
rownames(up_shared)
upshared_expt <- exclude_genes_expt(zy_norm, ids = rownames(up_shared), method = "keep")
```

We can plot a quick heatmap to get a sense of the differences observed
between the genes which are different between the two zymodemes.

### Heatmap of zymodeme gene expression increased in 2.3 vs. 2.2

```{r zymoempup}
high_23_heatmap <- plot_sample_heatmap(upshared_expt, row_label = rownames(up_shared))
high_23_heatmap
```

### Heatmap of zymodeme gene expression increased in 2.2 vs. 2.3

```{r zymoemdown}
down_shared <- shared_zymo[["downs"]][[1]][["data"]][["all"]]
downshared_expt <- exclude_genes_expt(zy_norm, ids = rownames(down_shared), method = "keep")
high_22_heatmap <- plot_sample_heatmap(downshared_expt, row_label = rownames(down_shared))
high_22_heatmap
```

# SNP profiles

Now I will combine our previous samples and our new samples in the
hopes of finding variant positions which help elucidate currently
unknown aspects of either group via their clustering to known samples
from the other group. In other words, we do not know the zymodeme
annotations for the old samples nor the strain identities (or the
shortcut 'chronic vs. self-healing') for the new samples. I hope to
make educated guesses given the variant profiles. There are some
differences in how the previous and current data sets were analyzed
(though I have since redone the old samples so it should be trivial to
remove those differences now).

I added our 2016 data to a specific TMRC2 sample sheet,
dated 20191203.  Thus I will load the data here.  That previous data
was mapped using tophat, so I will also need to make some changes to
the gene names to accomodate the two mappings.

```{r oldnew_variants}
old_expt <- sm(create_expt("sample_sheets/tmrc2_samples_20191203.xlsx",
                           file_column = "tophat2file"))

tt <- lp_expt[["expressionset"]]
rownames(tt) <- gsub(pattern = "^exon_", replacement = "", x = rownames(tt))
rownames(tt) <- gsub(pattern = "\\.E1$", replacement = "", x = rownames(tt))
lp_expt$expressionset <- tt

tt <- old_expt$expressionset
rownames(tt) <- gsub(pattern = "^exon_", replacement = "", x = rownames(tt))
rownames(tt) <- gsub(pattern = "\\.1$", replacement = "", x = rownames(tt))
old_expt$expressionset <- tt
rm(tt)
```

## Create the SNP expressionset

One other important caveat, we have a group of new samples which have
not yet run through the variant search pipeline, so I need to remove
them from consideration.  Though it looks like they finished overnight...

```{r count_expt_old_new}
## The next line drops the samples which are missing the SNP pipeline.
lp_snp <- subset_expt(lp_expt, subset="!is.na(pData(lp_expt)[['bcftable']])")
new_snps <- sm(count_expt_snps(lp_snp, annot_column = "bcftable"))
old_snps <- sm(count_expt_snps(old_expt, annot_column = "bcftable", snp_column = 2))

both_snps <- combine_expts(new_snps, old_snps)
both_norm <- sm(normalize_expt(both_snps, transform = "log2", convert = "cpm", filter = TRUE))

## strains <- both_norm[["design"]][["strain"]]
both_strain <- set_expt_conditions(both_norm, fact = "strain")
```

The data structure 'both_norm' now contains our 2016 data along with
the newer data collected since 2019.

## Plot of SNP profiles for zymodemes

The following plot shows the SNP profiles of all samples (old and new) where the
colors at the top show either the 2.2 strains (orange), 2.3 strains (green), the
previous samples (purple), or the various lab strains (pink etc).

```{r plotting_variants}
old_new_variant_heatmap <- plot_disheat(both_norm)
pp(file = "images/raw_snp_disheat.png", image = old_new_variant_heatmap,
   height = 12, width = 12)
```

The function get_snp_sets() takes the provided metadata factor (in
this case 'condition') and looks for variants which are exclusive to
each element in it.  In this case, this is looking for differences
between 2.2 and 2.3, as well as the set shared among them.

```{r get_snp_sets1}
snp_sets <- get_snp_sets(both_snps, factor = "condition")
both_expt <- combine_expts(lp_expt, old_expt)

snp_genes <- sm(snps_vs_genes(both_expt, snp_sets, expt_name_col = "chromosome"))
## I think we have some metrics here we can plot...
snp_subset <- sm(snp_subset_genes(
  both_expt, both_snps,
  genes = c("LPAL13_120010900", "LPAL13_340013000", "LPAL13_000054100",
            "LPAL13_140006100", "LPAL13_180018500", "LPAL13_320022300")))
zymo_heat <- plot_sample_heatmap(snp_subset, row_label = rownames(exprs(snp_subset)))
zymo_heat
```

Didn't I create a set of densities by chromosome?
Oh I think they come in from get_snp_sets()

## SNPS associated with clinical response in the TMRC samples

```{r snp_clinical}
clinical_sets <- get_snp_sets(new_snps, factor = "clinicalresponse")

density_vec <- clinical_sets[["density"]]
chromosome_idx <- grep(pattern = "LpaL", x = names(density_vec))
density_df <- as.data.frame(density_vec[chromosome_idx])
density_df[["chr"]] <- rownames(density_df)
colnames(density_df) <- c("density_vec", "chr")
ggplot(density_df, aes_string(x = "chr", y = "density_vec")) +
  ggplot2::geom_col() +
  ggplot2::theme(axis.text = ggplot2::element_text(size = 10, colour = "black"),
                 axis.text.x = ggplot2::element_text(angle = 90, vjust = 0.5))

## clinical_written <- write_variants(new_snps)
```

### Cross reference these variants by gene

```{r snp_classifications}
clinical_genes <- sm(snps_vs_genes(lp_expt, clinical_sets, expt_name_col = "chromosome"))

snp_density <- merge(as.data.frame(clinical_genes[["summary_by_gene"]]),
                     as.data.frame(fData(lp_expt)),
                     by = "row.names")
snp_density <- snp_density[, c(1, 2, 4, 15)]
colnames(snp_density) <- c("name", "snps", "product", "length")
snp_density[["product"]] <- tolower(snp_density[["product"]])
snp_density[["length"]] <- as.numeric(snp_density[["length"]])
snp_density[["density"]] <- snp_density[["snps"]] / snp_density[["length"]]
snp_idx <- order(snp_density[["density"]], decreasing = TRUE)
snp_density <- snp_density[snp_idx, ]

removers <- c("amastin", "gp63", "leishmanolysin")
for (r in removers) {
  drop_idx <- grepl(pattern = r, x = snp_density[["product"]])
  snp_density <- snp_density[!drop_idx, ]
}
## Filter these for [A|a]mastin gp63 Leishmanolysin
```


```{r snp_intersections}
clinical_snps <- snps_intersections(lp_expt, clinical_sets, chr_column = "chromosome")

fail_ref_snps <- as.data.frame(clinical_snps[["inters"]][["failure, reference strain"]])
cure_snps <- as.data.frame(clinical_snps[["inters"]][["cure"]])

head(fail_ref_snps)
head(cure_snps)

annot <- fData(lp_expt)
clinical_interest <- as.data.frame(clinical_snps[["gene_summaries"]][["cure"]])
clinical_interest <- merge(clinical_interest,
                           as.data.frame(clinical_snps[["gene_summaries"]][["failure, reference strain"]]),
                           by = "row.names")
rownames(clinical_interest) <- clinical_interest[["Row.names"]]
clinical_interest[["Row.names"]] <- NULL
colnames(clinical_interest) <- c("cure_snps","fail_snps")
annot <- merge(annot, clinical_interest, by = "row.names")
rownames(annot) <- annot[["Row.names"]]
annot[["Row.names"]] <- NULL
fData(lp_expt$expressionset) <- annot
```

# Zymodeme for new samples

The heatmap produced here should show the variants only for the zymodeme genes.

## Hunt for snp clusters

I am thinking that if we find clusters of locations which are variant, that
might provide some PCR testing possibilities.

```{r new_zymo}
new_sets <- get_snp_sets(new_snps, factor = "phenotypiccharacteristics")
summary(new_sets)
## 1000000: 2.2
## 0100000: 2.3

summary(new_sets[["intersections"]][["10000"]])
summary(new_sets[["intersections"]][["01000"]])
```

Thus we see that there are 511 variants associated with 2.2 and 49,790 associated with 2.3.

### A small function for searching for potential PCR primers

The following function uses the positional data to look for sequential
mismatches associated with zymodeme in the hopes that there will be
some regions which would provide good potential targets for a
PCR-based assay.

```{r sequential_search, eval=FALSE}
sequential_variants <- function(snp_sets, conditions = NULL, minimum = 3, maximum_separation = 3) {
  if (is.null(conditions)) {
    conditions <- 1
  }
  intersection_sets <- snp_sets[["intersections"]]
  intersection_names <- snp_sets[["set_names"]]
  chosen_intersection <- 1
  if (is.numeric(conditions)) {
    chosen_intersection <- conditions
  } else {
    intersection_idx <- intersection_names == conditions
    chosen_intersection <- names(intersection_names)[intersection_idx]
  }

  possible_positions <- intersection_sets[[chosen_intersection]]
  position_table <- data.frame(row.names = possible_positions)
  pat <- "^chr_(.+)_pos_(.+)_ref_.*$"
  position_table[["chr"]] <- gsub(pattern = pat, replacement = "\\1", x = rownames(position_table))
  position_table[["pos"]] <- as.numeric(gsub(pattern = pat, replacement = "\\2", x = rownames(position_table)))
  position_idx <- order(position_table[, "chr"], position_table[, "pos"])
  position_table <- position_table[position_idx, ]
  position_table[["dist"]] <- 0

  last_chr <- ""
  for (r in 1:nrow(position_table)) {
    this_chr <- position_table[r, "chr"]
    if (r == 1) {
      position_table[r, "dist"] <- position_table[r, "pos"]
      last_chr <- this_chr
      next
    }
    if (this_chr == last_chr) {
      position_table[r, "dist"] <- position_table[r, "pos"] - position_table[r - 1, "pos"]
    } else {
      position_table[r, "dist"] <- position_table[r, "pos"]
    }
    last_chr <- this_chr
  }

  ## Working interactively here.
  
  doubles <- position_table[["dist"]] == 1
  doubles <- position_table[doubles, ]
  write.csv(doubles, "doubles.csv")

  one_away <- position_table[["dist"]] == 2
  one_away <- position_table[one_away, ]
  write.csv(one_away, "one_away.csv")

  two_away <- position_table[["dist"]] == 3
  two_away <- position_table[two_away, ]
  write.csv(two_away, "two_away.csv")

  combined <- rbind(doubles, one_away)
  combined <- rbind(combined, two_away)
  position_idx <- order(combined[, "chr"], combined[, "pos"])
  combined <- combined[position_idx, ]
  
  this_chr <- ""
  for (r in 1:nrow(combined)) {
    this_chr <- combined[r, "chr"]
    if (r == 1) {
      combined[r, "dist_pair"] <- combined[r, "pos"]
      last_chr <- this_chr
      next
    }
    if (this_chr == last_chr) {
      combined[r, "dist_pair"] <- combined[r, "pos"] - combined[r - 1, "pos"]
    } else {
      combined[r, "dist_pair"] <- combined[r, "pos"]
    }
    last_chr <- this_chr
  }

  dist_pair_maximum <- 1000
  dist_pair_minimum <- 200
  dist_pair_idx <- combined[["dist_pair"]] <= dist_pair_maximum &
    combined[["dist_pair"]] >= dist_pair_minimum
  remaining <- combined[dist_pair_idx, ]
  no_weak_idx <- grepl(pattern="ref_(G|C)", x=rownames(remaining))
  remaining <- remaining[no_weak_idx, ]
  
  print(head(table(position_table[["dist"]])))
  sequentials <- position_table[["dist"]] <= maximum_separation
  message("There are ", sum(sequentials), " candidate regions.")

  ## The following can tell me how many runs of each length occurred, that is not quite what I want.
  ## Now use run length encoding to find the set of sequential sequentials!
  rle_result <- rle(sequentials)
  rle_values <- rle_result[["values"]]
  ## The following line is equivalent to just leaving values alone:
  ## true_values <- rle_result[["values"]] == TRUE
  rle_lengths <- rle_result[["lengths"]]
  true_sequentials <- rle_lengths[rle_values]
  rle_idx <- cumsum(rle_lengths)[which(rle_values)]

  position_table[["last_sequential"]] <- 0
  count <- 0
  for (r in rle_idx) {
    count <- count + 1
    position_table[r, "last_sequential"] <- true_sequentials[count]
  }
  message("The maximum sequential set is: ", max(position_table[["last_sequential"]]), ".")

  wanted_idx <- position_table[["last_sequential"]] >= minimum
  wanted <- position_table[wanted_idx, c("chr", "pos")]
  return(wanted)
}

zymo22_sequentials <- sequential_variants(new_sets, conditions = "22", minimum=1, maximum_separation=2)
dim(zymo22_sequentials)
## 7 candidate regions for zymodeme 2.2 -- thus I am betting that the reference strain is a 2.2
zymo23_sequentials <- sequential_variants(new_sets, conditions = "23",
                                          minimum = 2, maximum_separation = 2)
dim(zymo23_sequentials)
## In contrast, there are lots (587) of interesting regions for 2.3!
```

### Extract a promising region from the genome

The first 4 candidate regions from my set of remaining:
* Chr       Pos.   Distance
* LpaL13-15 238433 448
* LpaL13-18 142844 613
* LpaL13-29 830342 252
* LpaL13-33 1331507 843

Lets define a couple of terms:
* Third: Each of the 4 above positions.
* Second: Third - Distance
* End: Third + PrimerLen
* Start: Second - Primerlen

In each instance, these are the last positions, so we want to grab three things:

* The entire region from End -> Start, this way we can have a quick sanity check.
* Start -> Second.
* (Third -> End) <- Reverse complemented

```{r extract_bsgenome, eval=FALSE}
## * LpaL13-15 238433 448
first_candidate_chr <- genome[["LpaL13_15"]]
primer_length <- 22
amplicon_length <- 448
first_candidate_third <- 238433
first_candidate_second <- first_candidate_third - amplicon_length
first_candidate_start <- first_candidate_second - primer_length
first_candidate_end <- first_candidate_third + primer_length
first_candidate_region <- subseq(first_candidate_chr, first_candidate_start, first_candidate_end)
first_candidate_region
first_candidate_5p <- subseq(first_candidate_chr, first_candidate_start, first_candidate_second)
as.character(first_candidate_5p)
first_candidate_3p <- spgs::reverseComplement(subseq(first_candidate_chr, first_candidate_third, first_candidate_end))
first_candidate_3p


## * LpaL13-18 142844 613
second_candidate_chr <- genome[["LpaL13_18"]]
primer_length <- 22
amplicon_length <- 613
second_candidate_third <- 142844
second_candidate_second <- second_candidate_third - amplicon_length
second_candidate_start <- second_candidate_second - primer_length
second_candidate_end <- second_candidate_third + primer_length
second_candidate_region <- subseq(second_candidate_chr, second_candidate_start, second_candidate_end)
second_candidate_region
second_candidate_5p <- subseq(second_candidate_chr, second_candidate_start, second_candidate_second)
as.character(second_candidate_5p)
second_candidate_3p <- spgs::reverseComplement(subseq(second_candidate_chr, second_candidate_third, second_candidate_end))
second_candidate_3p


## * LpaL13-29 830342 252
third_candidate_chr <- genome[["LpaL13_29"]]
primer_length <- 22
amplicon_length <- 252
third_candidate_third <- 830342
third_candidate_second <- third_candidate_third - amplicon_length
third_candidate_start <- third_candidate_second - primer_length
third_candidate_end <- third_candidate_third + primer_length
third_candidate_region <- subseq(third_candidate_chr, third_candidate_start, third_candidate_end)
third_candidate_region
third_candidate_5p <- subseq(third_candidate_chr, third_candidate_start, third_candidate_second)
as.character(third_candidate_5p)
third_candidate_3p <- spgs::reverseComplement(subseq(third_candidate_chr, third_candidate_third, third_candidate_end))
third_candidate_3p
## You are a garbage polypyrimidine tract.
## Which is actually interesting if the mutations mess it up.


## * LpaL13-33 1331507 843
fourth_candidate_chr <- genome[["LpaL13_33"]]
primer_length <- 22
amplicon_length <- 843
fourth_candidate_third <- 1331507
fourth_candidate_second <- fourth_candidate_third - amplicon_length
fourth_candidate_start <- fourth_candidate_second - primer_length
fourth_candidate_end <- fourth_candidate_third + primer_length
fourth_candidate_region <- subseq(fourth_candidate_chr, fourth_candidate_start, fourth_candidate_end)
fourth_candidate_region
fourth_candidate_5p <- subseq(fourth_candidate_chr, fourth_candidate_start, fourth_candidate_second)
as.character(fourth_candidate_5p)
fourth_candidate_3p <- spgs::reverseComplement(subseq(fourth_candidate_chr, fourth_candidate_third, fourth_candidate_end))
fourth_candidate_3p
```

## Go hunting for Sanger sequencing regions

I made a fun little function which should find regions which have lots of variants
associated with a given experimental factor.

```{r sanger_fun, eval=FALSE}
pheno <- subset_expt(lp_expt, subset = "condition=='z2.2'|condition=='z2.3'")
pheno <- subset_expt(pheno, subset = "!is.na(pData(pheno)[['bcftable']])")
pheno_snps <- sm(count_expt_snps(pheno, annot_column = "bcftable"))

fun_stuff <- snp_density_primers(pheno_snps,
                                 bsgenome="BSGenome.Leishmania.panamensis.MHOMCOL81L13.v53",
                                 gff="reference/TriTrypDB-53_LpanamensisMHOMCOL81L13.gff")
drop_scaffolds <- grepl(x = rownames(fun_stuff$favorites), pattern = "SCAF")
favorite_primer_regions <- fun_stuff[["favorites"]][!drop_scaffolds, ]
favorite_primer_regions[["bin"]] <- rownames(favorite_primer_regions)
library(dplyr)
favorite_primer_regions <- favorite_primer_regions %>%
  relocate(bin)
```

## Combine this table with 2.2/2.3 genes

Here is my note from our meeting:

Cross reference primers to DE genes of 2.2/2.3 and/or resistance/suscpetible,
add a column to the primer spreadsheet with the DE genes (in retrospect I am guessing
this actually means to put the logFC as a column.

One nice thing, I did a semantic removal on the lp_expt, so the set of logFC/pvalues
should not have any of the offending types; thus I should be able to automagically
get rid of them in the merge.

```{r xref_primers_deg}
logfc <- zy_table[["data"]][["z23_vs_z22"]]
logfc_columns <- logfc[, c("deseq_logfc", "deseq_adjp")]
colnames(logfc_columns) <- c("z23_logfc", "z23_adjp")
new_table <- merge(favorite_primer_regions, logfc_columns,
                   by.x = "closest_gene_before_id", by.y = "row.names")
sus <- sus_table[["data"]][["sensitive_vs_resistant"]]
sus_columns <- sus[, c("deseq_logfc", "deseq_adjp")]
colnames(sus_columns) <- c("sus_logfc", "sus_adjp")
new_table <- merge(new_table, sus_columns,
                   by.x = "closest_gene_before_id", by.y = "row.names") %>%
  relocate(bin)
written <- write_xlsx(data=new_table,
                      excel="excel/favorite_primers_xref_zy_sus.
```


## Make a heatmap describing the clustering of variants

We can cross reference the variants against the zymodeme status and
plot a heatmap of the results and hopefully see how they separate.

```{r zymo_heatmaps}
snp_genes <- sm(snps_vs_genes(lp_expt, new_sets, expt_name_col = "chromosome"))
new_zymo_norm <- normalize_expt(new_snps, filter = TRUE, convert = "cpm", norm = "quant", transform = TRUE)
new_zymo_norm <- set_expt_conditions(new_zymo_norm, fact = "phenotypiccharacteristics")

zymo_heat <- plot_disheat(new_zymo_norm)
zymo_heat[["plot"]]
```

### Annotated heatmap of variants

Now let us try to make a heatmap which includes some of the annotation data.

```{r zymo_heat_panel_genes}
des <- both_norm[["design"]]
undef_idx <- is.na(des[["strain"]])
des[undef_idx, "strain"] <- "unknown"

##hmcols <- colorRampPalette(c("yellow","black","darkblue"))(256)
correlations <- hpgl_cor(exprs(both_norm))

zymo_missing_idx <- is.na(des[["phenotypiccharacteristics"]])
des[["phenotypiccharacteristics"]] <- as.character(des[["phenotypiccharacteristics"]])
des[["clinicalcategorical"]] <- as.character(des[["clinicalcategorical"]])
des[zymo_missing_idx, "phenotypiccharacteristics"] <- "unknown"
mydendro <- list(
  "clustfun" = hclust,
  "lwd" = 2.0)
col_data <- as.data.frame(des[, c("phenotypiccharacteristics", "clinicalcategorical")])

unknown_clinical <- is.na(col_data[["clinicalcategorical"]])
row_data <- as.data.frame(des[, c("strain")])
colnames(col_data) <- c("zymodeme", "outcome")
col_data[unknown_clinical, "outcome"] <- "undefined"

colnames(row_data) <- c("strain")
myannot <- list(
  "Col" = list("data" = col_data),
  "Row" = list("data" = row_data))
myclust <- list("cuth" = 1.0,
                "col" = BrewerClusterCol)
mylabs <- list(
  "Row" = list("nrow" = 4),
  "Col" = list("nrow" = 4))
hmcols <- colorRampPalette(c("darkblue", "beige"))(240)
map1 <- annHeatmap2(
  correlations,
  dendrogram = mydendro,
  annotation = myannot,
  cluster = myclust,
  labels = mylabs,
  ## The following controls if the picture is symmetric
  scale = "none",
  col = hmcols)
pp(file = "images/dendro_heatmap.png", image = map1, height = 20, width = 20)
```

Print the larger heatmap so that all the labels appear.  Keep in mind
that as we get more samples, this image needs to continue getting
bigger.

![big heatmap](images/dendro_heatmap.png)


```{r theresa_idea}

xref_prop <- table(pheno_snps[["conditions"]])
pheno_snps$conditions
idx_tbl <- exprs(pheno_snps) > 5
new_tbl <- data.frame(row.names = rownames(exprs(pheno_snps)))
for (n in names(xref_prop)) {
  new_tbl[[n]] <- 0
  idx_cols <- which(pheno_snps[["conditions"]] == n)
  prop_col <- rowSums(idx_tbl[, idx_cols]) / xref_prop[n]
  new_tbl[n] <- prop_col
}
keepers <- grepl(x = rownames(new_tbl), pattern = "LpaL13")
new_tbl <- new_tbl[keepers, ]
new_tbl[["strong22"]] <- 1.001 - new_tbl[["z2.2"]]
new_tbl[["strong23"]] <- 1.001 - new_tbl[["z2.3"]]
s22_na <- new_tbl[["strong22"]] > 1
new_tbl[s22_na, "strong22"] <- 1
s23_na <- new_tbl[["strong23"]] > 1
new_tbl[s23_na, "strong23"] <- 1

new_tbl[["SNP"]] <- rownames(new_tbl)
new_tbl[["Chromosome"]] <- gsub(x = new_tbl[["SNP"]], pattern = "chr_(.*)_pos_.*", replacement = "\\1")
new_tbl[["Position"]] <- gsub(x = new_tbl[["SNP"]], pattern = ".*_pos_(\\d+)_.*", replacement = "\\1")
new_tbl <- new_tbl[, c("SNP", "Chromosome", "Position", "strong22", "strong23")]


library(CMplot)
simplify <- new_tbl
simplify[["strong22"]] <- NULL


CMplot(simplify, bin.size = 100000)

CMplot(new_tbl, plot.type="m", multracks=TRUE, threshold = c(0.01, 0.05),
       threshold.lwd=c(1,1), threshold.col=c("black","grey"),
       amplify=TRUE, bin.size=10000,
       chr.den.col=c("darkgreen", "yellow", "red"),
       signal.col=c("red", "green", "blue"),
       signal.cex=1, file="jpg", memo="", dpi=300, file.output=TRUE, verbose=TRUE)
```

![SNP Density](SNP-Density.ratio.jpg)
![Circular Manhattan](Circular-Manhattan.ratio.jpg)
![Rectangular Manhattan](Rectangular-Manhattan.ratio.jpg)
![QQ](QQplot.ratio.jpg)

## Try out MatrixEQTL

This tool looks a little opaque, but provides sample data with things
that make sense to me and should be pretty easy to recapitulate in our
data.

1.  covariates.txt: Columns are samples, rows are things from pData -- the
    most likely ones of interest for our data would be zymodeme,
    sensitivity
2.  geneloc.txt: columns are 'geneid', 'chr', 'left', 'right'.  I
    guess I can assume left and right are start/stop; in which case
    this is trivially acquirable from fData.
3.  ge.txt: This appears to be a log(rpkm/cpm) table with rows as genes and
    columns as samples
4.  snpsloc.txt: columns are 'snpid', 'chr', 'pos'
5.  snps.txt: columns are samples, rows are the ids from snsploc,
    values a 0,1,2.  I assume 0 is identical and 1..12 are the various
    A->TGC T->AGC C->AGT G->ACT

```{r matrixeqtl, eval=FALSE}
## For this, let us use the 'new_snps' data structure.
## Caveat here: these need to be coerced to numbers.
my_covariates <- pData(new_snps)[, c("phenotypiccharacteristics", "clinicalcategorical")]
for (col in colnames(my_covariates)) {
  my_covariates[[col]] <- as.numeric(as.factor(my_covariates[[col]]))
}
my_covariates <- t(my_covariates)

my_geneloc <- fData(lp_expt)[, c("gid", "chromosome", "start", "end")]
colnames(my_geneloc) <- c("geneid", "chr", "left", "right")

my_ge <- exprs(normalize_expt(lp_expt, transform = "log2", filter = TRUE, convert = "cpm"))
used_samples <- tolower(colnames(my_ge)) %in% colnames(exprs(new_snps))
my_ge <- my_ge[, used_samples]

my_snpsloc <- data.frame(rownames = rownames(exprs(new_snps)))
## Oh, caveat here: Because of the way I stored the data,
## I could have duplicate rows which presumably will make matrixEQTL sad
my_snpsloc[["chr"]] <- gsub(pattern = "^chr_(.+)_pos(.+)_ref_.*$", replacement = "\\1",
                            x = rownames(my_snpsloc))
my_snpsloc[["pos"]] <- gsub(pattern = "^chr_(.+)_pos(.+)_ref_.*$", replacement = "\\2",
                            x = rownames(my_snpsloc))
test <- duplicated(my_snpsloc)
## Each duplicated row would be another variant at that position;
## so in theory we would do a rle to number them I am guessing
## However, I do not have different variants so I think I can ignore this for the moment
## but will need to make my matrix either 0 or 1.
if (sum(test) > 0) {
  message("There are: ", sum(duplicated), " duplicated entries.")
  keep_idx <- ! test
  my_snpsloc <- my_snpsloc[keep_idx, ]
}

my_snps <- exprs(new_snps)
one_idx <- my_snps > 0
my_snps[one_idx] <- 1

## Ok, at this point I think I have all the pieces which this method wants...
## Oh, no I guess not; it actually wants the data as a set of filenames...
library(MatrixEQTL)
write.table(my_snps, "eqtl/snps.tsv", na = "NA", col.names = TRUE, row.names = TRUE, sep = "\t", quote = TRUE)
## readr::write_tsv(my_snps, "eqtl/snps.tsv", )
write.table(my_snpsloc, "eqtl/snpsloc.tsv", na = "NA", col.names = TRUE, row.names = TRUE, sep = "\t", quote = TRUE)
## readr::write_tsv(my_snpsloc, "eqtl/snpsloc.tsv")
write.table(as.data.frame(my_ge), "eqtl/ge.tsv", na = "NA", col.names = TRUE, row.names = TRUE, sep = "\t", quote = TRUE)
## readr::write_tsv(as.data.frame(my_ge), "eqtl/ge.tsv")
write.table(as.data.frame(my_geneloc), "eqtl/geneloc.tsv", na = "NA", col.names = TRUE, row.names = TRUE, sep = "\t", quote = TRUE)
## readr::write_tsv(as.data.frame(my_geneloc), "eqtl/geneloc.tsv")
write.table(as.data.frame(my_covariates), "eqtl/covariates.tsv", na = "NA", col.names = TRUE, row.names = TRUE, sep = "\t", quote = TRUE)
## readr::write_tsv(as.data.frame(my_covariates), "eqtl/covariates.tsv")

useModel = modelLINEAR # modelANOVA, modelLINEAR, or modelLINEAR_CROSS

# Genotype file name
SNP_file_name = "eqtl/snps.tsv"
snps_location_file_name = "eqtl/snpsloc.tsv"
expression_file_name = "eqtl/ge.tsv"
gene_location_file_name = "eqtl/geneloc.tsv"
covariates_file_name = "eqtl/covariates.tsv"
# Output file name
output_file_name_cis = tempfile()
output_file_name_tra = tempfile()
# Only associations significant at this level will be saved
pvOutputThreshold_cis = 0.1
pvOutputThreshold_tra = 0.1
# Error covariance matrix
# Set to numeric() for identity.
errorCovariance = numeric()
# errorCovariance = read.table("Sample_Data/errorCovariance.txt");
# Distance for local gene-SNP pairs
cisDist = 1e6
## Load genotype data
snps = SlicedData$new()
snps$fileDelimiter = "\t"      # the TAB character
snps$fileOmitCharacters = "NA" # denote missing values;
snps$fileSkipRows = 1          # one row of column labels
snps$fileSkipColumns = 1       # one column of row labels
snps$fileSliceSize = 2000      # read file in slices of 2,000 rows
snps$LoadFile(SNP_file_name)
## Load gene expression data
gene = SlicedData$new()
gene$fileDelimiter = "\t"      # the TAB character
gene$fileOmitCharacters = "NA" # denote missing values;
gene$fileSkipRows = 1          # one row of column labels
gene$fileSkipColumns = 1       # one column of row labels
gene$fileSliceSize = 2000      # read file in slices of 2,000 rows
gene$LoadFile(expression_file_name)
## Load covariates
cvrt = SlicedData$new()
cvrt$fileDelimiter = "\t"      # the TAB character
cvrt$fileOmitCharacters = "NA" # denote missing values;
cvrt$fileSkipRows = 1          # one row of column labels
cvrt$fileSkipColumns = 1       # one column of row labels
if(length(covariates_file_name) > 0) {
  cvrt$LoadFile(covariates_file_name)
}
## Run the analysis
snpspos = read.table(snps_location_file_name, header = TRUE, stringsAsFactors = FALSE)
genepos = read.table(gene_location_file_name, header = TRUE, stringsAsFactors = FALSE)

me = Matrix_eQTL_main(
    snps = snps,
    gene = gene,
    cvrt = cvrt,
    output_file_name = output_file_name_tra,
    pvOutputThreshold = pvOutputThreshold_tra,
    useModel = useModel,
    errorCovariance = errorCovariance,
    verbose = TRUE,
    output_file_name.cis = output_file_name_cis,
    pvOutputThreshold.cis = pvOutputThreshold_cis,
    snpspos = snpspos,
    genepos = genepos,
    cisDist = cisDist,
    pvalue.hist = "qqplot",
    min.pv.by.genesnp = FALSE,
    noFDRsaveMemory = FALSE);
```



```{r saveme}
if (!isTRUE(get0("skip_load"))) {
  pander::pander(sessionInfo())
  message(paste0("This is hpgltools commit: ", get_git_commit()))
  message(paste0("Saving to ", savefile))
  tmp <- sm(saveme(filename = savefile))
}
```

```{r loadme_after, eval = FALSE}
tmp <- loadme(filename = savefile)
```


TMRC2 Comprehensive Data Analysis: 202108

atb abelew@gmail.com

2021-08-23