Mercurial > repos > iuc > ruvseq
comparison get_deseq_dataset.R @ 0:61dffb20b6f9 draft
planemo upload for repository https://github.com/galaxyproject/tools-iuc/tree/master/tools/ruvseq commit b95582cea8320d5488056a9576474f79cec53be8
author | iuc |
---|---|
date | Wed, 05 Sep 2018 15:54:16 -0400 |
parents | |
children | c24765926774 |
comparison
equal
deleted
inserted
replaced
-1:000000000000 | 0:61dffb20b6f9 |
---|---|
1 get_deseq_dataset <- function(sampleTable, header, designFormula, tximport, txtype, tx2gene) { | |
2 | |
3 dir <- "" | |
4 | |
5 if (!is.null(header)) { | |
6 hasHeader <- TRUE | |
7 } else { | |
8 hasHeader <- FALSE | |
9 } | |
10 | |
11 if (!is.null(tximport)) { | |
12 if (is.null(tx2gene)) stop("A transcript-to-gene map or a GTF file is required for tximport") | |
13 if (tolower(file_ext(opt$tx2gene)) == "gtf") { | |
14 gtfFile <-tx2gene | |
15 } else { | |
16 gtfFile <- NULL | |
17 tx2gene <- read.table(tx2gene, header=FALSE) | |
18 } | |
19 useTXI <- TRUE | |
20 } else { | |
21 useTXI <- FALSE | |
22 } | |
23 | |
24 if (!useTXI & hasHeader) { | |
25 countfiles <- lapply(as.character(sampleTable$filename), function(x){read.delim(x, row.names=1)}) | |
26 tbl <- do.call("cbind", countfiles) | |
27 colnames(tbl) <- rownames(sampleTable) # take sample ids from header | |
28 | |
29 # check for htseq report lines (from DESeqDataSetFromHTSeqCount function) | |
30 oldSpecialNames <- c("no_feature", "ambiguous", "too_low_aQual", | |
31 "not_aligned", "alignment_not_unique") | |
32 specialRows <- (substr(rownames(tbl), 1, 1) == "_") | rownames(tbl) %in% oldSpecialNames | |
33 tbl <- tbl[!specialRows, , drop = FALSE] | |
34 | |
35 dds <- DESeqDataSetFromMatrix(countData = tbl, | |
36 colData = subset(sampleTable, select=-(filename)), | |
37 design = designFormula) | |
38 } else if (!useTXI & !hasHeader) { | |
39 | |
40 # construct the object from HTSeq files | |
41 dds <- DESeqDataSetFromHTSeqCount(sampleTable = sampleTable, | |
42 directory = dir, | |
43 design = designFormula) | |
44 colnames(dds) <- row.names(sampleTable) | |
45 | |
46 } else { | |
47 # construct the object using tximport | |
48 # first need to make the tx2gene table | |
49 # this takes ~2-3 minutes using Bioconductor functions | |
50 if (!is.null(gtfFile)) { | |
51 suppressPackageStartupMessages({ | |
52 library("GenomicFeatures") | |
53 }) | |
54 txdb <- makeTxDbFromGFF(gtfFile, format="gtf") | |
55 k <- keys(txdb, keytype = "GENEID") | |
56 df <- select(txdb, keys = k, keytype = "GENEID", columns = "TXNAME") | |
57 tx2gene <- df[, 2:1] # tx ID, then gene ID | |
58 } | |
59 library("tximport") | |
60 txiFiles <- as.character(sampleTable$filename) | |
61 labs <- row.names(sampleTable) | |
62 names(txiFiles) <- labs | |
63 txi <- tximport(txiFiles, type=txtype, tx2gene=tx2gene) | |
64 dds <- DESeqDataSetFromTximport(txi, | |
65 subset(sampleTable, select=-c(filename)), | |
66 designFormula) | |
67 } | |
68 return(dds) | |
69 } |