Description Usage Arguments Value
HTSeq-count output a tab-delimed count file, while the first column records
gene_id, and the second column records raw read count. read_htseq
merges multiple HTSeq-count output into one matrix. The count files could be
selected using Sys.glob
.
1 | read_htseq(files, labels = NULL, clean = TRUE)
|
files |
HTSeq-count output files |
labels |
sample labels used as colnames in count matrix |
clean |
clean meta-line (start with '__') or not |
a count matrix, with rows as genes and columns as samples
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