Description Usage Arguments Value Backward compatibility Author(s) References
Calls the htseq-count executable to count input reads on features.
1 2 3 4 | ## Default S3 method:
htseqCount(pathnameS, gff, orderedBy=c("none", "position", "name"),
sortByName=c("always", "auto"), optionsVec=c(`-s` = "no", `-a` = "10"), ...,
pathnameD=NULL, command="htseq-count", verbose=FALSE)
|
pathnameS |
An input BAM or SAM file containing aligned reads. |
gff |
The gene feature file, in GFF/GTF format. |
orderedBy |
A |
sortByName |
A |
optionsVec |
A named |
... |
(Not used) |
pathnameD |
(optional) destination file to save htseq-count output. |
command |
A |
verbose |
See |
Returns what systemHTSeqCount
() returns.
htseq-count
(< 0.6.0) requires (i) a SAM file as input
that (ii) is sorted by name. However, this method will take care of
that internally, iff needed. That is, it will created a temporary SAM
file that is sorted by query name before passing it to htseq-count
.
Taku Tokuyasu, Henrik Bengtsson
[1] S Anders, TP Pyl, W Huber,
HTSeq - A Python framework to work with high-throughput sequencing data.
bioRxiv 2014. doi: 10.1101/002824.
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