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parse the htseq output as a tibble with columns (feature, sample). This code is copied from the National Cancer Institute GenomicDataCommons

Usage

readHTSeqFile(htseq_filename, samplename = "sample")

Arguments

htseq_filename

filepath to htseq output

samplename

in the legacy pipeline, the fastqFileName with .fastq.gz replaced with _read_count.tsv

Value

a dataframe with columns feature, 'sample'