Thank you for your reply I have human rna sequence( paired ) so from where I get this gff file for this and then what the command I have to follow
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htseq-count -f bam -r name -i gene_id -s no -t exon /Users/abc/sorted.bam > count.txt
usage: htseq-count [options] alignment_file gff_file htseq-count: error: the following arguments are required: featuresfilename
not getting what's wrong in my code help me
You give the software no gff. How is it supposed to assign reads to genes without one?
Thank you for your reply I have human rna sequence( paired ) so from where I get this gff file for this and then what the command I have to follow
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