Mercurial > repos > vipints > deseq_hts
view deseq-hts_1.0/src/difftest_deseq.R @ 2:8ac6832cb42c draft
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author | vipints |
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date | Wed, 27 Jun 2012 15:37:03 -0400 |
parents | 94a108763d9e |
children | e27b4f7811c2 |
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library( DESeq ) ### get arguments 1: INFILE, 2: OUTFILE 3:SIZE args <- commandArgs() INFILE<-args[4] OUTFILE<-args[5] INFILE_COUNTS=c(paste(INFILE, "_COUNTS.tab", sep="")) INFILE_CONDS=c(paste(INFILE, "_CONDITIONS.tab", sep="")) ### read count data from file countsTable <- read.delim( INFILE_COUNTS, header=TRUE, stringsAsFactors=TRUE ) condsTable <- read.delim( INFILE_CONDS, header=TRUE, stringsAsFactors=TRUE ) ### use gene IDs as row names rownames( countsTable ) <- countsTable$gene countsTable <- countsTable[ , -1 ] head( countsTable ) conds <- factor( condsTable[ , 2] ) #head( countsTable ) cds <- newCountDataSet( round(countsTable), conds ) #head( counts(cds) ) cds <- estimateSizeFactors( cds ) #sizeFactors( cds ) ### estimate variance function, use blind only, if no replicates are provided if (length(levels(conds)) < length(conds)) { cds <- estimateDispersions( cds ) } else { writeLines("\nYou did not enter any replicates! - The results may be less valuable without replicates!\n") cds <- estimateDispersions( cds, method='blind', sharingMode='fit-only') } experiments <- levels(conds) res<-c() table_col_names<-c() for (i in 1:(length(experiments)-1)) { for( j in (i+1):(length(experiments))) { print(c(i,j)) tempres <- nbinomTest(cds,experiments[i],experiments[j]) res = cbind(res,tempres[,7]) #res = cbind(res,tempres[,8]) table_col_names = cbind(table_col_names,paste('cond_', experiments[i], '_vs._cond_', experiments[j], sep='')) } } DiffTable<-res rownames(DiffTable)<-rownames(countsTable) colnames(DiffTable)<-table_col_names write.table(DiffTable, file = OUTFILE, quote = FALSE, sep ="\t", eol ="\n", na = "1.000", dec = ".", row.names = TRUE,col.names =TRUE)