After alignment small RNA sequence to the reference genome using bowtie. I got SAM file, then how to calculate read counts? What's the criterion? Is there software to do this work?
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featureCounts (and htseq-count) count features based on the annotation file you provide. Provide locations of the smallRNA's you are interested in (GTF format) to get the counts you want.
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Originally posted by GenoMax View PostfeatureCounts (and htseq-count) count features based on the annotation file you provide. Provide locations of the smallRNA's you are interested in (GTF format) to get the counts you want.
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Originally posted by GenoMax View PostfeatureCounts (and htseq-count) count features based on the annotation file you provide. Provide locations of the smallRNA's you are interested in (GTF format) to get the counts you want.
I analysis small RNA of switchgrass. It has not GTF file of small RNA. The reference genome of switchgrass has not assemble completely yet. In this situation, is there any other software I can use to caculate read counts? Thank you very much.
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Sounds like you are doing your alignments against the genome (incomplete assembly)?
See if this site can help: http://smallrna.udel.edu/index.php
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