TMRC2 Comprehensive Data Analysis: 202106

sample_sheet <- glue::glue("sample_sheets/tmrc2_samples_20210620.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:

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.

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 TODO:

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

4 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.

4.1 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’

4.2 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.

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 = 8600) %>%
  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 8600 non-zero genes are:

## TMRC20002 TMRC20004 TMRC20006 TMRC20029 TMRC20008 
##  11681227    564812   6670348   1658096   6249790

## subset_expt(): There were 74, now there are 69 samples.

## semantic_expt_filter(): Removed 68 genes.

libsizes <- plot_libsize(lp_expt)
pp(file = "images/lp_expt_libsizes.png", image = libsizes$plot, width = 12, height = 9)

## I think samples 7,10 should be removed at minimum, probably also 9,11
nonzero <- plot_nonzero(lp_expt)
nonzero$plot

## Warning: ggrepel: 45 unlabeled data points (too many overlaps). Consider
## increasing max.overlaps

lp_box <- plot_boxplot(lp_expt)

## 5042 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

4.3 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’.

4.4 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_samples <- lp_expt %>%
  set_expt_batches(fact = sus_categorical)

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")

## Removing 144 low-count genes (8566 remaining).

## batch_counts: Before batch/surrogate estimation, 904 entries are x==0: 0%.

## batch_counts: Before batch/surrogate estimation, 3181 entries are 0<x<1: 1%.

## Setting 349 low elements to zero.

## transform_counts: Found 349 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: ggrepel: 1 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.

4.5 By Cure/Fail status

cf_expt <- set_expt_conditions(lp_expt, fact = "clinicalcategorical") %>%
  set_expt_batches(fact = sus_categorical)

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

## Removing 144 low-count genes (8566 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 144 low-count genes (8566 remaining).

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

## batch_counts: Before batch/surrogate estimation, 3869 entries are 0<x<1: 1%.

## Setting 185 low elements to zero.

## transform_counts: Found 185 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 144 low-count genes (8566 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 0.1111934 0.33404 8.018e-03 0.02413 0.47581 0.592902
## zymodemecategorical 0.0005176 0.74336 1.232e-01 0.42741 0.43642 0.062042
## pathogenstrain      0.7086904 0.55723 3.573e-05 0.10951 0.02648 0.340918
## passagenumber       0.2663969 0.00033 3.641e-02 0.15180 0.03254 0.000199

test$cor_heatmap

sus_expt <- set_expt_conditions(lp_expt, fact = "sus_category") %>%
  set_expt_batches(fact = "zymodemecategorical")

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

## Removing 144 low-count genes (8566 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 144 low-count genes (8566 remaining).

## batch_counts: Before batch/surrogate estimation, 904 entries are x==0: 0%.

## batch_counts: Before batch/surrogate estimation, 3181 entries are 0<x<1: 1%.

## Setting 217 low elements to zero.

## transform_counts: Found 217 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’.

5 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.

5.1 Differential expression

5.1.1 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 69, 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")))

5.1.2 Images of zymodeme DE

zy_table[["plots"]][["z23_vs_z22"]][["deseq_ma_plots"]][["plot"]]

5.2 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")))

5.3 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	annotgeneentrezid	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_p	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_000044900	LPAL13_000044900	actin-related protein 2, putative	protein coding	LPAL13_SCAF000645	507	1685	-			reverse	Not Assigned	1179.0	1178	28.790	0e+00	13.450	0.0000	9.1400	0.2589	3.9680	-4.1900	15.758	0.1218	8.1590	10.190	0.0000	0.0000	867.100	1.1860	24.290	0	117203.26	16.839	0.0000	1172.023	813.905	5.037e+05	327.867	1.0000	0e+00	1.0000	4.9820	55.270	0.0000	1.3800	1.5830	-4.3100	0.1182	2.588e-01	3.794e-126	2.374e-10	0.000e+00	1.028e-07	14.700	7.202e+00	4.899e-01	3.940e-02	4.657e-03
LPAL13_350020000	LPAL13_350020000	hypothetical protein, conserved	protein coding	LpaL13_35	484442	484858	-			reverse	35	417.0	416	17.500	0e+00	2.942	0.0493	-0.2957	0.6963	-4.5670	-4.1900	3.211	0.1218	-0.3763	-1.008	0.3224	0.4835	4.138	1.1860	14.750	0	294.37	8.201	0.0000	2.934	2.037	9.619e+01	1.618	1.0000	0e+00	1.0000	-2.9030	6.485	0.0109	-4.5860	-0.6233	-4.8550	0.5352	8.534e-01	2.079e-45	5.396e-02	0.000e+00	4.998e-01	5.380	5.332e+01	9.910e+00	1.820e-01	9.358e-02
LPAL13_190021900	LPAL13_190021900	hypothetical protein, conserved	protein coding	LpaL13_19	595931	597058	-			reverse	19	1128.0	1127	15.810	0e+00	1.768	0.2763	-0.5523	0.4411	-5.0370	-4.1900	3.376	0.1218	-0.8466	-2.215	0.0352	0.1021	4.940	1.4840	10.660	0	515.35	9.009	0.0000	5.144	3.572	4.312e+02	2.597	1.0000	0e+00	1.0000	-2.8270	2.303	0.1291	-4.7900	-1.1280	-4.6280	0.2634	5.553e-01	2.793e-23	2.761e-01	0.000e+00	1.424e-01	4.609	5.058e+01	1.097e+01	1.308e-01	1.735e-02
LPAL13_000035800	LPAL13_000035800	hypothetical protein	protein coding	LPAL13_SCAF000500	737	1006	-			reverse	Not Assigned	270.0	269	14.830	0e+00	14.040	0.0000	10.4400	0.3129	5.3280	-3.9500	15.105	0.4187	9.2790	11.580	0.0000	0.0000	2937.000	1.1750	12.620	0	29229.70	14.835	0.1385	4339.174	3013.358	1.388e+07	1210.588	0.0000	0e+00	0.0000	6.7360	79.660	0.0000	2.3090	1.4270	-4.4450	0.1583	3.145e-01	7.141e-33	3.808e-15	0.000e+00	1.011e-08	15.280	1.846e+01	1.209e+00	5.277e-02	8.353e-03
LPAL13_320026300	LPAL13_320026300	hypothetical protein, conserved	protein coding	LpaL13_32	754268	755485	-			reverse	32	1218.0	1217	14.070	0e+00	13.230	0.0000	9.9100	0.3245	4.7860	-4.0160	18.218	0.7007	8.8020	9.888	0.0000	0.0000	1581.000	1.1460	12.280	0	16393.43	14.001	0.1294	2285.921	1587.485	2.058e+06	618.456	0.0000	0e+00	0.0000	5.8450	71.220	0.0000	2.0570	1.3970	-4.4710	0.1671	3.261e-01	2.635e-31	1.367e-13	0.000e+00	5.579e-08	12.060	3.904e+00	3.237e-01	5.570e-02	9.307e-03
LPAL13_000051300	LPAL13_000051300	hypothetical protein, conserved	protein coding	LPAL13_SCAF000772	11	2344	+			forward	Not Assigned	2334.0	2333	8.967	0e+00	9.591	0.0000	3.8260	0.2711	0.2400	-3.9870	10.249	0.5655	4.2270	6.223	0.0000	0.0000	143.300	1.2930	6.937	0	1623.33	10.665	0.0951	170.535	118.456	6.846e+04	52.767	0.0000	0e+00	0.0000	2.4300	31.780	0.0000	-1.0670	1.5430	-4.3460	0.1275	3.418e-01	1.942e-09	1.628e-06	0.000e+00	3.848e-05	7.556	4.714e+00	6.239e-01	4.250e-02	5.419e-03
LPAL13_000053200	LPAL13_000053200	hypothetical protein	protein coding	LPAL13_SCAF000804	5037	5249	-			reverse	Not Assigned	213.0	212	8.808	0e+00	10.230	0.0000	5.8820	0.0404	1.0040	-4.1900	9.085	0.1218	5.1940	8.488	0.0000	0.0000	78.670	1.1190	7.873	0	12683.94	13.631	0.0000	126.829	88.076	7.967e+03	36.176	1.0000	0e+00	1.0000	1.5630	48.860	0.0000	-0.9051	2.7470	-2.9650	0.0077	4.049e-02	2.700e-12	1.331e-09	0.000e+00	9.009e-07	9.230	3.524e+00	3.818e-01	2.565e-03	1.974e-05
LPAL13_000040700	LPAL13_000040700	hypothetical protein, conserved	protein coding	LPAL13_SCAF000598	54	1067	+			forward	Not Assigned	1014.0	1013	6.621	0e+00	8.066	0.0000	2.9160	0.1304	-1.2440	-4.1900	6.505	0.1218	2.9470	5.658	0.0000	0.0002	21.230	1.1850	5.589	0	2601.37	11.345	0.0000	26.004	18.058	4.051e+02	7.843	1.0000	0e+00	1.0000	-0.1262	29.820	0.0000	-2.3940	2.0710	-3.8370	0.0422	1.303e-01	2.394e-06	3.756e-06	0.000e+00	1.737e-04	5.924	2.243e+00	3.786e-01	1.407e-02	5.936e-04
LPAL13_000017600	LPAL13_000017600	hypothetical protein, conserved	protein coding	LPAL13_SCAF000146	359	586	+			forward	Not Assigned	228.0	227	6.561	0e+00	6.541	0.0000	5.8580	0.0947	4.4470	-1.1880	4.357	2.8136	5.6350	8.593	0.0000	0.0000	641.800	0.6968	9.416	0	80.11	6.324	12.0678	967.579	675.617	3.961e+05	63.477	0.0000	1e+00	0.0000	4.5460	53.840	0.0000	2.3770	2.2720	-3.4020	0.0263	9.437e-02	9.787e-18	2.802e-10	9.782e-01	1.186e-06	7.024	5.957e+00	8.482e-01	8.770e-03	2.307e-04
LPAL13_300029400	LPAL13_300029400	hypothetical protein, conserved	protein coding	LpaL13_30	853953	854150	-			reverse	30	198.0	197	6.188	0e+00	6.104	0.0000	4.8200	0.0056	1.7310	-2.3560	1.486	1.8118	4.0860	8.631	0.0000	0.0000	90.410	0.7565	8.179	0	59.50	5.895	2.0963	125.321	87.669	9.233e+03	22.740	0.0000	1e+00	0.0000	1.7260	47.780	0.0000	0.0613	3.6880	-1.0330	0.0005	6.288e-03	4.385e-13	1.950e-09	9.220e-01	9.535e-06	5.956	9.318e-01	1.564e-01	1.510e-04	6.840e-08
LPAL13_080010600	LPAL13_080010600	hypothetical protein, conserved	protein coding	LpaL13_08	195555	195749	-			reverse	8	195.0	194	6.085	0e+00	7.559	0.0000	2.3050	0.0851	-1.8760	-4.1900	4.928	0.1218	2.3150	5.072	0.0000	0.0005	11.600	1.1850	5.135	0	1847.08	10.851	0.0000	18.461	12.820	4.800e+02	6.091	1.0000	0e+00	1.0000	-0.9235	25.500	0.0000	-3.1370	2.3350	-3.5650	0.0226	1.065e-01	2.046e-05	2.278e-05	0.000e+00	7.148e-04	5.036	4.676e+00	9.285e-01	7.517e-03	1.695e-04
LPAL13_000011700	LPAL13_000011700	hypothetical protein	protein coding	LPAL13_SCAF000076	101	364	-			reverse	Not Assigned	264.0	263	6.023	0e+00	7.515	0.0000	2.6230	0.0730	-1.3920	-4.1900	6.768	0.1218	2.7980	5.271	0.0000	0.0004	14.620	1.2020	5.009	0	2444.22	11.255	0.0000	24.432	16.967	4.690e+02	7.539	1.0000	0e+00	1.0000	-0.5872	24.350	0.0000	-2.9280	2.4220	-3.4300	0.0181	8.226e-02	3.391e-05	3.780e-05	0.000e+00	5.174e-04	4.986	1.302e+00	2.610e-01	6.037e-03	1.093e-04
LPAL13_040019400	LPAL13_040019400	hypothetical protein	protein coding	LpaL13_04	440768	441127	-			reverse	4	360.0	359	5.619	0e+00	5.475	0.0000	3.4630	0.0330	-0.4122	-3.4870	1.700	1.1787	3.0750	7.348	0.0000	0.0000	35.230	0.9680	5.804	0	48.41	5.597	0.6939	34.070	23.871	1.800e+03	8.712	0.0000	0e+00	0.0000	0.3962	28.430	0.0000	-1.6470	2.8520	-2.8270	0.0058	3.288e-02	8.378e-07	6.754e-06	0.000e+00	1.261e-05	4.858	5.010e-02	1.031e-02	1.921e-03	1.107e-05
LPAL13_350011800	LPAL13_350011800	hypothetical protein, conserved	protein coding	LpaL13_35	171009	171242	+			forward	35	234.0	233	5.114	0e+00	5.092	0.0000	4.2440	0.0085	2.8760	-0.8274	2.432	0.1624	3.7030	11.060	0.0000	0.0000	180.500	0.5840	8.757	0	31.92	4.997	9.4332	301.450	212.223	5.943e+04	24.041	0.0000	1e+00	0.0000	2.7130	52.890	0.0000	1.2340	3.4990	-0.9341	0.0008	8.501e-03	3.221e-15	3.187e-10	9.139e-01	7.140e-09	4.970	1.003e+00	2.017e-01	2.770e-04	2.301e-07
LPAL13_080010800	LPAL13_080010800	hypothetical protein	protein coding	LpaL13_08	199409	199792	-			reverse	8	384.0	383	5.103	1e-04	6.605	0.0000	1.6340	0.2740	-2.3530	-4.1900	4.142	0.1218	1.8380	4.371	0.0002	0.0020	10.840	1.0900	4.681	0	1048.70	10.034	0.0000	10.477	7.276	1.077e+02	3.577	1.0000	0e+00	1.0000	-0.8700	24.340	0.0000	-3.1120	1.5350	-4.3530	0.1294	3.452e-01	8.581e-05	3.781e-05	0.000e+00	2.099e-03	4.021	3.492e+00	8.685e-01	4.313e-02	5.581e-03
LPAL13_170014500	LPAL13_170014500	hypothetical protein, conserved	protein coding	LpaL13_17	361708	362040	+			forward	17	333.0	332	5.076	0e+00	4.987	0.0003	2.7700	0.0577	-0.6435	-3.1940	6.976	1.6024	2.5510	3.914	0.0004	0.0040	22.230	0.9987	5.082	0	43.02	5.427	1.0218	44.379	31.131	1.643e+03	10.334	0.0000	0e+00	0.0000	-0.2522	18.620	0.0000	-2.3990	2.5520	-3.1990	0.0130	5.776e-02	1.753e-05	3.458e-04	0.000e+00	5.619e-03	4.250	5.433e-03	1.278e-03	4.329e-03	5.600e-05
LPAL13_200050100	LPAL13_200050100	hypothetical protein	protein coding	LpaL13_20.1	1627529	1627717	+			forward	20.1	189.0	188	4.805	0e+00	4.777	0.0000	4.8970	0.0029	2.4590	-1.9470	1.007	2.4930	4.4060	8.528	0.0000	0.0000	121.100	0.6203	7.746	0	26.30	4.717	7.3797	194.359	137.226	2.167e+04	18.260	0.0000	1e+00	0.0000	2.1650	42.950	0.0000	0.8115	3.9780	-0.2381	0.0002	2.978e-03	6.748e-12	1.553e-08	9.782e-01	3.559e-05	5.158	3.490e+00	6.767e-01	5.737e-05	9.873e-09
LPAL13_000011800	LPAL13_000011800	hypothetical protein, conserved	protein coding	LPAL13_SCAF000076	446	640	-			reverse	Not Assigned	195.0	194	4.650	3e-04	5.124	0.0006	1.0280	0.4707	-2.5010	-3.9760	3.657	0.6133	1.4750	3.282	0.0024	0.0148	11.660	1.0740	4.330	0	56.34	5.816	0.1523	9.134	6.389	7.337e+01	2.950	0.9995	5e-04	0.9995	-0.8430	17.460	0.0000	-3.0630	1.0660	-4.6780	0.2901	4.710e-01	4.381e-04	5.725e-04	1.052e-02	1.691e-02	3.222	3.146e+00	9.765e-01	9.671e-02	2.805e-02
LPAL13_000014000	LPAL13_000014000	hypothetical protein	protein coding	LPAL13_SCAF000119	655	942	+			forward	Not Assigned	288.0	287	4.385	0e+00	4.368	0.0000	3.9720	0.0193	2.4360	-1.2160	1.511	2.0003	3.6520	7.419	0.0000	0.0000	131.400	0.5415	8.097	0	19.75	4.304	9.7344	192.485	136.645	1.297e+04	14.798	0.0000	1e+00	0.0000	2.2840	48.520	0.0000	1.1030	3.1230	-1.8390	0.0026	2.154e-02	7.791e-13	1.472e-09	9.782e-01	5.140e-05	4.454	1.205e+00	2.705e-01	8.787e-04	2.316e-06
LPAL13_000026500	LPAL13_000026500	hypothetical protein	protein coding	LPAL13_SCAF000301	144	494	-			reverse	Not Assigned	351.0	350	4.326	0e+00	4.262	0.0001	2.3650	0.2373	0.1451	-2.4630	5.401	2.0725	2.6080	4.101	0.0003	0.0031	46.180	0.8041	5.380	0	21.34	4.415	2.5893	55.452	39.299	1.544e+03	9.481	0.0000	0e+00	0.0000	0.9106	22.390	0.0000	-0.8720	1.6500	-4.2470	0.1035	2.971e-01	4.800e-06	8.635e-05	0.000e+00	3.664e-03	3.528	1.101e-01	3.122e-02	3.450e-02	3.571e-03

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

	gid	annotgeneproduct	annotgenetype	chromosome	start	end	strand	annotgeneentrezid	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_p	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	-5.322	0.0007	-5.223	0.0020	-5.983	0.0000	-3.7320	3.4740	10.6232	0.0632	-7.206	-10.980	0	0e+00	132.20	1.2910	-4.124	0.0000	0.1238	-3.013	311.93	38.621	122.131	2.245e+04	0.1327	0.0000	0.0000	0.0000	2.2630	14.420	0.0001	-1.1130	-5.851	5.7350	0e+00	2.516e-05	8.893e-04	1.987e-03	0.000e+00	2.663e-08	-5.509	0.000e+00	0.000e+00	6.127e-05	5.779e-09
LPAL13_000038400	LPAL13_000038400	expression-site associated gene (esag3), putative	protein coding	LPAL13_SCAF000573	101	1360	+			forward	Not Assigned	1260.0	1259	-2.799	0.0000	-2.809	0.0000	-3.316	0.0001	4.6320	8.2380	3.1190	0.0291	-3.606	-10.100	0	0e+00	3715.00	0.5536	-5.056	0.0000	0.1737	-2.526	8823.76	1532.426	3760.333	1.554e+07	0.1785	0.0000	0.0000	0.0000	7.0750	28.830	0.0000	5.8210	-5.237	4.7890	0e+00	1.258e-04	2.334e-05	5.627e-06	0.000e+00	7.122e-08	-2.958	9.900e-03	-3.347e-03	7.520e-07	7.760e-13
LPAL13_350063000	LPAL13_350063000	hypothetical protein	protein coding	LpaL13_35	1964328	1964543	-			reverse	35	216.0	215	-2.781	0.0000	-2.773	0.0000	-3.437	0.0000	-2.3210	1.2090	2.1742	0.2275	-3.530	-10.760	0	0e+00	21.51	0.4794	-5.801	0.0000	0.1384	-2.853	55.15	7.623	22.146	6.307e+02	0.1596	0.0000	1.0000	0.0000	-0.3596	32.400	0.0000	-1.4690	-6.951	8.4370	0e+00	2.404e-06	7.052e-07	1.210e-06	1.000e+00	7.140e-09	-3.001	1.424e-04	-4.744e-05	6.983e-09	2.915e-17
LPAL13_140019300	LPAL13_140019300	bt1 family, putative	protein coding	LpaL13_14	530784	531350	+			forward	14	567.0	566	-2.639	0.0000	-2.644	0.0000	-2.458	0.0000	4.6450	7.0660	0.4796	1.1129	-2.421	-6.978	0	2e-04	1878.00	0.3824	-6.901	0.0000	0.1702	-2.555	4611.26	784.782	1953.985	5.164e+06	0.1758	0.0000	1.0000	0.0000	6.0910	54.610	0.0000	5.3840	-6.676	10.3300	0e+00	3.699e-06	1.409e-09	2.374e-10	1.000e+00	1.516e-04	-2.635	1.954e-01	-7.417e-02	1.855e-09	1.029e-17
LPAL13_000012000	LPAL13_000012000	hypothetical protein	protein coding	LPAL13_SCAF000080	710	1159	-			reverse	Not Assigned	450.0	449	-2.602	0.0007	-2.610	0.0004	-3.114	0.0031	0.1005	3.9570	7.6499	0.1802	-3.856	-6.792	0	0e+00	210.50	0.6351	-4.097	0.0000	0.2237	-2.160	451.41	100.977	208.054	4.893e+04	0.2352	0.1870	0.8130	0.1870	2.9370	18.490	0.0000	1.3640	-3.956	0.6667	2e-04	3.089e-03	8.965e-04	3.655e-04	7.672e-01	1.860e-05	-2.741	3.114e-02	-1.136e-02	8.143e-05	8.259e-09
LPAL13_310039200	LPAL13_310039200	hypothetical protein	protein coding	LpaL13_31	1301745	1301972	-			reverse	31	228.0	227	-2.372	0.0000	-2.379	0.0000	-2.403	0.0000	1.2220	3.7790	1.3487	0.2180	-2.557	-9.416	0	0e+00	195.60	0.4028	-5.888	0.0000	0.2457	-2.025	396.35	97.357	188.716	3.434e+04	0.2570	0.4434	0.5566	0.4434	2.8330	37.170	0.0000	2.0290	-5.735	6.6830	0e+00	3.061e-05	6.831e-07	1.937e-07	6.151e-01	2.663e-08	-2.489	1.173e-01	-4.714e-02	8.503e-08	2.044e-14
LPAL13_000012100	LPAL13_000012100	hypothetical protein	protein coding	LPAL13_SCAF000080	1637	1894	-			reverse	Not Assigned	258.0	257	-2.248	0.0096	-2.249	0.0089	-3.387	0.0004	-2.2050	1.2020	6.3050	0.6808	-3.407	-6.079	0	0e+00	31.28	0.6975	-3.223	0.0013	0.2746	-1.865	66.02	18.121	32.755	1.805e+03	0.3056	0.0536	0.9464	0.0536	0.2198	10.740	0.0010	-1.4250	-4.811	2.5060	0e+00	3.761e-04	9.729e-03	8.888e-03	9.371e-01	4.288e-05	-2.655	4.154e-02	-1.565e-02	7.749e-04	4.519e-07
LPAL13_310031000	LPAL13_310031000	hypothetical protein, conserved	protein coding	LpaL13_31	1075172	1075459	-			reverse	31	288.0	287	-2.241	0.0000	-2.241	0.0000	-2.859	0.0000	-2.0160	1.0070	3.4877	0.5506	-3.023	-6.944	0	0e+00	26.73	0.4390	-5.104	0.0000	0.2698	-1.890	55.87	15.064	27.532	1.035e+03	0.2953	0.1254	0.8746	0.1254	0.0391	26.060	0.0000	-1.2030	-6.166	6.4050	0e+00	1.323e-05	1.587e-05	1.825e-05	9.127e-01	4.714e-06	-2.487	2.700e-03	-1.085e-03	2.354e-07	2.736e-14
LPAL13_340039600	LPAL13_340039600	hypothetical protein	protein coding	LpaL13_34	1247554	1247757	-			reverse	34	204.0	203	-2.208	0.0004	-2.215	0.0002	-2.697	0.0014	1.2470	4.2040	3.6334	0.0559	-2.958	-7.626	0	0e+00	225.10	0.5166	-4.275	0.0000	0.2254	-2.149	518.32	116.820	239.500	4.536e+04	0.2307	0.0000	1.0000	0.0000	3.0230	20.280	0.0000	1.9620	-4.284	1.6790	1e-04	1.406e-03	5.729e-04	1.808e-04	9.782e-01	4.567e-06	-2.359	1.405e-02	-5.958e-03	2.846e-05	7.653e-10
LPAL13_310035500	LPAL13_310035500	hypothetical protein	protein coding	LpaL13_31	1198439	1198957	-			reverse	31	519.0	518	-2.169	0.0265	-2.123	0.0227	-3.429	0.0000	-4.1830	-0.3803	4.1409	0.4809	-3.802	-8.310	0	0e+00	7.27	0.7714	-2.812	0.0049	0.2939	-1.767	18.43	5.409	9.386	3.219e+02	0.3480	0.0000	0.0000	0.0000	-1.9310	8.444	0.0037	-3.1810	-6.740	5.7090	0e+00	3.053e-06	3.767e-02	2.266e-02	0.000e+00	3.015e-07	-2.558	1.427e-01	-5.579e-02	2.864e-03	6.553e-06
LPAL13_310031300	LPAL13_310031300	hypothetical protein, conserved	protein coding	LpaL13_31	1084772	1085059	-			reverse	31	288.0	287	-1.983	0.0034	-1.986	0.0032	-3.070	0.0003	-1.0680	2.0860	3.9512	0.7614	-3.154	-6.616	0	0e+00	63.55	0.5516	-3.595	0.0003	0.2465	-2.020	130.45	32.149	62.186	5.901e+03	0.2667	0.0527	0.9473	0.0527	1.2070	13.220	0.0003	-0.2180	-4.845	3.0360	0e+00	3.404e-04	4.648e-03	3.217e-03	8.854e-01	9.612e-06	-2.320	2.907e-02	-1.253e-02	2.033e-04	2.923e-08
LPAL13_140019100	LPAL13_140019100	bt1 family, putative	protein coding	LpaL13_14	525164	525514	+			forward	14	351.0	350	-1.955	0.0000	-1.960	0.0000	-2.011	0.0000	3.9170	5.9980	0.3503	0.5491	-2.081	-8.231	0	0e+00	885.30	0.3037	-6.435	0.0000	0.2333	-2.100	1937.62	451.965	905.916	6.953e+05	0.2374	0.0000	1.0000	0.0000	5.0060	49.810	0.0000	4.5800	-7.140	12.2000	0e+00	1.185e-06	4.354e-08	9.680e-10	9.139e-01	2.321e-05	-1.977	6.493e-02	-3.284e-02	3.148e-10	1.946e-19
LPAL13_050005000	LPAL13_050005000	hypothetical protein	protein coding	LpaL13_05	3394	3612	-			reverse	5	219.0	218	-1.936	0.0085	-1.942	0.0054	-2.728	0.0003	0.1998	2.6770	2.0583	0.1721	-2.477	-7.913	0	0e+00	91.42	0.5913	-3.275	0.0011	0.2820	-1.826	177.99	50.188	89.238	6.186e+03	0.2912	0.0006	0.9994	0.0006	1.7220	11.960	0.0005	0.4951	-4.939	3.6870	0e+00	3.023e-04	1.047e-02	5.406e-03	9.782e-01	9.009e-07	-2.176	2.023e-02	-9.296e-03	5.357e-04	2.765e-07
LPAL13_000038500	LPAL13_000038500	hypothetical protein	protein coding	LPAL13_SCAF000575	39	251	+			forward	Not Assigned	213.0	212	-1.919	0.0126	-1.926	0.0190	-3.310	0.0001	-1.9280	1.4320	4.6678	0.6770	-3.360	-6.743	0	0e+00	32.43	0.6149	-3.122	0.0018	0.2833	-1.820	77.47	21.939	38.905	2.414e+03	0.3098	0.1589	0.8411	0.1589	0.2246	8.871	0.0029	-1.3010	-5.462	4.3980	0e+00	7.805e-05	1.249e-02	2.088e-02	8.530e-01	7.838e-06	-2.243	1.477e-01	-6.584e-02	1.566e-03	2.139e-06
LPAL13_340039700	LPAL13_340039700	snare domain containing protein, putative	protein coding	LpaL13_34	1248192	1248947	-			reverse	34	756.0	755	-1.757	0.0000	-1.764	0.0000	-1.884	0.0000	4.6120	6.6510	0.6865	0.0521	-2.038	-11.360	0	0e+00	1384.00	0.3134	-5.606	0.0000	0.2859	-1.806	2810.80	803.689	1416.973	1.132e+06	0.2899	0.0000	1.0000	0.0000	5.6510	36.560	0.0000	5.2460	-6.216	8.5080	0e+00	1.131e-05	1.689e-06	2.435e-07	9.788e-01	5.841e-09	-1.792	1.985e-02	-1.108e-02	1.949e-08	3.035e-16
LPAL13_170015400	LPAL13_170015400	hypothetical protein, conserved	protein coding	LpaL13_17	395975	396307	+			forward	17	333.0	332	-1.608	0.0000	-1.615	0.0000	-1.672	0.0001	1.2490	3.2680	0.9405	0.1360	-2.019	-9.032	0	0e+00	153.70	0.2829	-5.684	0.0000	0.3146	-1.669	270.09	84.958	141.528	1.297e+04	0.3199	0.0000	1.0000	0.0000	2.4770	33.070	0.0000	2.0470	-5.245	4.8990	0e+00	1.550e-04	1.689e-06	1.051e-06	9.782e-01	6.425e-08	-1.673	2.122e-02	-1.269e-02	5.724e-07	9.452e-13
LPAL13_350073400	LPAL13_350073400	hypothetical protein	protein coding	LpaL13_35	2342701	2342883	+			forward	35	183.0	182	-1.517	0.0077	-1.521	0.0079	-2.098	0.0006	-0.1050	1.8100	0.9225	0.8801	-1.915	-5.600	0	4e-04	48.25	0.4575	-3.315	0.0009	0.3090	-1.694	113.46	35.053	59.011	6.521e+03	0.3352	0.0008	0.9992	0.0008	0.7712	11.050	0.0009	-0.0586	-4.629	2.5210	0e+00	7.422e-04	1.092e-02	8.673e-03	9.782e-01	4.687e-04	-1.746	1.203e-02	-6.891e-03	6.072e-04	2.613e-07
LPAL13_350013200	LPAL13_350013200	hypothetical protein, conserved	protein coding	LpaL13_35	223837	224070	+			forward	35	234.0	233	-1.501	0.0055	-1.502	0.0083	-2.047	0.0003	-2.0500	-0.1507	1.3400	0.7031	-1.899	-5.540	0	2e-04	10.97	0.4373	-3.432	0.0006	0.3587	-1.479	24.88	8.918	13.796	2.950e+02	0.3917	0.7799	0.2201	0.7799	-1.1530	10.920	0.0010	-2.0910	-4.904	2.1990	0e+00	2.971e-04	6.838e-03	8.365e-03	2.576e-01	2.400e-04	-1.672	5.433e-03	-3.250e-03	5.189e-04	2.281e-07
LPAL13_140019200	LPAL13_140019200	inositol-3-phosphate synthase	protein coding	LpaL13_14	527711	529291	+		INO1	forward	14	1581.0	1580	-1.449	0.0000	-1.456	0.0000	-1.517	0.0000	8.8250	10.3900	0.1716	0.4791	-1.564	-6.967	0	2e-04	19470.00	0.2714	-5.341	0.0000	0.3510	-1.510	36839.50	12931.785	20236.920	1.798e+08	0.3541	0.0000	1.0000	0.0000	9.4650	44.890	0.0000	9.2430	-6.495	9.6440	0e+00	6.144e-06	4.912e-06	7.137e-09	1.000e+00	2.369e-04	-1.517	4.357e-03	-2.873e-03	3.475e-08	2.541e-15
LPAL13_320038700	LPAL13_320038700	hypothetical protein, conserved	protein coding	LpaL13_32	1175024	1175257	+			forward	32	234.0	233	-1.417	0.0000	-1.424	0.0000	-1.412	0.0000	2.5510	3.9570	0.4252	0.1118	-1.406	-8.528	0	0e+00	262.40	0.2333	-6.074	0.0000	0.4144	-1.271	436.05	180.701	258.724	2.162e+04	0.4183	0.0011	0.9989	0.0011	3.2550	39.100	0.0000	3.0070	-5.752	6.8070	0e+00	3.038e-05	2.830e-07	9.066e-08	9.220e-01	1.867e-07	-1.443	1.145e-02	-7.937e-03	7.848e-08	1.809e-14

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)

5.4 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))

5.4.1 A couple plots from the differential expression

5.4.1.1 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"]]

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

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

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

zy_go_up$pvalue_plots$bpp_plot_over

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

zy_go_down$pvalue_plots$bpp_plot_over

5.5 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 = -136, df = 8542, p-value <2e-16
## alternative hypothesis: true correlation is not equal to 0
## 95 percent confidence interval:
##  -0.8343 -0.8210
## sample estimates:
##     cor 
## -0.8278

5.6 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:

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.

5.6.1 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

5.7 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.

5.7.1 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

5.7.2 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

6 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)

6.1 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 69, now there are 65 samples.

new_snps <- sm(count_expt_snps(lp_snp, annot_column = "bcftable"))

## Error : 'preprocessing/TMRC20063/outputs/vcfutils_lpanamensis_v36/r1_trimmed_lpanamensis_v36_count.txt' does not exist in current working directory ('/mnt/cbcb/fs01_abelew/cbcb-lab/nelsayed/scratch/atb/rnaseq/lpanamensis_tmrc_2019').
## Error : 'preprocessing/TMRC20063/outputs/vcfutils_lpanamensis_v36/r1_trimmed_lpanamensis_v36_count.txt' does not exist in current working directory ('/mnt/cbcb/fs01_abelew/cbcb-lab/nelsayed/scratch/atb/rnaseq/lpanamensis_tmrc_2019').

## Error in Biobase::`sampleNames<-`(`*tmp*`, value = colnames(snp_exprs)): number of new names (64) should equal number of rows in AnnotatedDataFrame (65)

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

both_snps <- combine_expts(new_snps, old_snps)

## Error in combine_expts(new_snps, old_snps): object 'new_snps' not found

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

## Error in normalize_expt(both_snps, transform = "log2", convert = "cpm", : object 'both_snps' not found

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

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

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

6.2 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)

## Error in plot_heatmap(expt_data, expt_colors = expt_colors, expt_design = expt_design, : object 'both_norm' not found

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

## Error in pp(file = "images/raw_snp_disheat.png", image = old_new_variant_heatmap, : object 'old_new_variant_heatmap' not found

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")

## Error in get_snp_sets(both_snps, factor = "condition"): object 'both_snps' not found

both_expt <- combine_expts(lp_expt, old_expt)

snp_genes <- sm(snps_vs_genes(both_expt, snp_sets, expt_name_col = "chromosome"))

## Error in snps_vs_genes(both_expt, snp_sets, expt_name_col = "chromosome"): object 'snp_sets' not found

## 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")))

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

zymo_heat <- plot_sample_heatmap(snp_subset, row_label = rownames(exprs(snp_subset)))

## Error in plot_sample_heatmap(snp_subset, row_label = rownames(exprs(snp_subset))): object 'snp_subset' not found

zymo_heat

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

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

6.3 SNPS associated with clinical response in the TMRC samples

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

## Error in get_snp_sets(new_snps, factor = "clinicalresponse"): object 'new_snps' not found

density_vec <- clinical_sets[["density"]]

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

chromosome_idx <- grep(pattern = "LpaL", x = names(density_vec))

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

density_df <- as.data.frame(density_vec[chromosome_idx])

## Error in h(simpleError(msg, call)): error in evaluating the argument 'x' in selecting a method for function 'as.data.frame': object 'density_vec' not found

density_df[["chr"]] <- rownames(density_df)

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

colnames(density_df) <- c("density_vec", "chr")

## Error in colnames(density_df) <- c("density_vec", "chr"): object 'density_df' not found

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))

## Error in ggplot(density_df, aes_string(x = "chr", y = "density_vec")): object 'density_df' not found

## clinical_written <- write_variants(new_snps)

6.3.1 Cross reference these variants by gene

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

## Error in snps_vs_genes(lp_expt, clinical_sets, expt_name_col = "chromosome"): object 'clinical_sets' not found

snp_density <- merge(as.data.frame(clinical_genes[["summary_by_gene"]]),
                     as.data.frame(fData(lp_expt)),
                     by = "row.names")

## Error in h(simpleError(msg, call)): error in evaluating the argument 'x' in selecting a method for function 'merge': error in evaluating the argument 'x' in selecting a method for function 'as.data.frame': object 'clinical_genes' not found

snp_density <- snp_density[, c(1, 2, 4, 15)]

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

colnames(snp_density) <- c("name", "snps", "product", "length")

## Error in colnames(snp_density) <- c("name", "snps", "product", "length"): object 'snp_density' not found

snp_density[["product"]] <- tolower(snp_density[["product"]])

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

snp_density[["length"]] <- as.numeric(snp_density[["length"]])

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

snp_density[["density"]] <- snp_density[["snps"]] / snp_density[["length"]]

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

snp_idx <- order(snp_density[["density"]], decreasing = TRUE)

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

snp_density <- snp_density[snp_idx, ]

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

removers <- c("amastin", "gp63", "leishmanolysin")
for (r in removers) {
  drop_idx <- grepl(pattern = r, x = snp_density[["product"]])
  snp_density <- snp_density[!drop_idx, ]
}

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

## Filter these for [A|a]mastin gp63 Leishmanolysin

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

## Error in snps_intersections(lp_expt, clinical_sets, chr_column = "chromosome"): object 'clinical_sets' not found

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

## Error in h(simpleError(msg, call)): error in evaluating the argument 'x' in selecting a method for function 'as.data.frame': object 'clinical_snps' not found

cure_snps <- as.data.frame(clinical_snps[["inters"]][["cure"]])

## Error in h(simpleError(msg, call)): error in evaluating the argument 'x' in selecting a method for function 'as.data.frame': object 'clinical_snps' not found

head(fail_ref_snps)

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

head(cure_snps)

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

annot <- fData(lp_expt)
clinical_interest <- as.data.frame(clinical_snps[["gene_summaries"]][["cure"]])

## Error in h(simpleError(msg, call)): error in evaluating the argument 'x' in selecting a method for function 'as.data.frame': object 'clinical_snps' not found

clinical_interest <- merge(clinical_interest,
                           as.data.frame(clinical_snps[["gene_summaries"]][["failure, reference strain"]]),
                           by = "row.names")

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

rownames(clinical_interest) <- clinical_interest[["Row.names"]]

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

clinical_interest[["Row.names"]] <- NULL

## Error in clinical_interest[["Row.names"]] <- NULL: object 'clinical_interest' not found

colnames(clinical_interest) <- c("cure_snps","fail_snps")

## Error in colnames(clinical_interest) <- c("cure_snps", "fail_snps"): object 'clinical_interest' not found

annot <- merge(annot, clinical_interest, by = "row.names")

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

rownames(annot) <- annot[["Row.names"]]
annot[["Row.names"]] <- NULL
fData(lp_expt$expressionset) <- annot

7 Zymodeme for new samples

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

7.1 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")

## Error in get_snp_sets(new_snps, factor = "phenotypiccharacteristics"): object 'new_snps' not found

summary(new_sets)

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

## 1000000: 2.2
## 0100000: 2.3

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

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

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

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

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

7.1.1 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
  }

  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")

## Error in sequential_variants(new_sets, conditions = "22"): object 'new_sets' not found

dim(zymo22_sequentials)

## Error in eval(expr, envir, enclos): object 'zymo22_sequentials' not found

## 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 = 1, maximum_separation = 3)

## Error in sequential_variants(new_sets, conditions = "23", minimum = 1, : object 'new_sets' not found

dim(zymo23_sequentials)

## Error in eval(expr, envir, enclos): object 'zymo23_sequentials' not found

## In contrast, there are lots (587) of interesting regions for 2.3!

7.2 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"))

## Error in snps_vs_genes(lp_expt, new_sets, expt_name_col = "chromosome"): object 'new_sets' not found

new_zymo_norm  <- normalize_expt(new_snps, filter = TRUE, convert = "cpm", norm = "quant", transform = TRUE)

## Error in normalize_expt(new_snps, filter = TRUE, convert = "cpm", norm = "quant", : object 'new_snps' not found

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

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

zymo_heat <- plot_disheat(new_zymo_norm)

## Error in plot_heatmap(expt_data, expt_colors = expt_colors, expt_design = expt_design, : object 'new_zymo_norm' not found

zymo_heat[["plot"]]

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

7.2.1 Annotated heatmap of variants

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

des <- both_norm[["design"]]

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

undef_idx <- is.na(des[["strain"]])

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

des[undef_idx, "strain"] <- "unknown"

## Error in des[undef_idx, "strain"] <- "unknown": object 'des' not found

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

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

zymo_missing_idx <- is.na(des[["phenotypiccharacteristics"]])

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

des[["phenotypiccharacteristics"]] <- as.character(des[["phenotypiccharacteristics"]])

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

des[["clinicalcategorical"]] <- as.character(des[["clinicalcategorical"]])

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

des[zymo_missing_idx, "phenotypiccharacteristics"] <- "unknown"

## Error in des[zymo_missing_idx, "phenotypiccharacteristics"] <- "unknown": object 'des' not found

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

## Error in h(simpleError(msg, call)): error in evaluating the argument 'x' in selecting a method for function 'as.data.frame': object 'des' not found

unknown_clinical <- is.na(col_data[["clinicalcategorical"]])

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

row_data <- as.data.frame(des[, c("strain")])

## Error in h(simpleError(msg, call)): error in evaluating the argument 'x' in selecting a method for function 'as.data.frame': object 'des' not found

colnames(col_data) <- c("zymodeme", "outcome")

## Error in colnames(col_data) <- c("zymodeme", "outcome"): object 'col_data' not found

col_data[unknown_clinical, "outcome"] <- "undefined"

## Error in col_data[unknown_clinical, "outcome"] <- "undefined": object 'col_data' not found

colnames(row_data) <- c("strain")

## Error in colnames(row_data) <- c("strain"): object 'row_data' not found

myannot <- list(
  "Col" = list("data" = col_data),
  "Row" = list("data" = row_data))

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

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)

## Error in annHeatmap2(correlations, dendrogram = mydendro, annotation = myannot, : object 'correlations' not found

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

## Error in pp(file = "images/dendro_heatmap.png", image = map1, height = 20, : object 'map1' not found

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

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

## subset_expt(): There were 69, now there are 34 samples.

pheno <- subset_expt(pheno, subset="!is.na(pData(pheno)[['bcftable']])")

## subset_expt(): There were 34, now there are 31 samples.

pheno_snps <- sm(count_expt_snps(pheno, annot_column = "bcftable"))

## Error : 'preprocessing/TMRC20063/outputs/vcfutils_lpanamensis_v36/r1_trimmed_lpanamensis_v36_count.txt' does not exist in current working directory ('/mnt/cbcb/fs01_abelew/cbcb-lab/nelsayed/scratch/atb/rnaseq/lpanamensis_tmrc_2019').
## Error : 'preprocessing/TMRC20063/outputs/vcfutils_lpanamensis_v36/r1_trimmed_lpanamensis_v36_count.txt' does not exist in current working directory ('/mnt/cbcb/fs01_abelew/cbcb-lab/nelsayed/scratch/atb/rnaseq/lpanamensis_tmrc_2019').

## Error in Biobase::`sampleNames<-`(`*tmp*`, value = colnames(snp_exprs)): number of new names (30) should equal number of rows in AnnotatedDataFrame (31)

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

CMplot(new_tbl, bin.size = 100000)

## Error in is.data.frame(x): object 'new_tbl' 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=1e5,
       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

7.3 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

## 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 f80b9b77ce0f5b0c13e9172e5cf51a94eaadaa9e

## This is hpgltools commit: Mon Jun 28 14:14:28 2021 -0400: f80b9b77ce0f5b0c13e9172e5cf51a94eaadaa9e

## Saving to tmrc2_02sample_estimation_v202106.rda.xz

tmp <- loadme(filename = savefile)