htseqCount | R Documentation |
compiles read count hits
htseqCount(df, promNames = c("rRNA", "Mt_rRNA", "protein_coding",
"__no_feature", " __ambiguous", "__too_low_aQual", "__not_aligned",
"__alignment_not_unique"))
df |
data.frame that results from htseq-count |
promNames |
vector of features names of interest |
data.frame of feature, proportion of reads mapping to this feature
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