I am very new to bioinformatics, so I would be really grateful for some help!
I have been using HTSeq Count v0.5.3 and I am bit confused about how the stranded options work. I have used both -s no and -s yes and for a few genes the number in the stranded set are higher than in the non-stranded set (and I haven't changed anything else). Looking in the genome browser, I think this is because in -s yes mode those reads for which the mate maps to a different gene or maps ambiguously are counted, whereas -s no ignores these. My data is stranded, so I want to use the stranded mode, but if that means that I am including reads where the mates map improperly, am I better off excluding these from the data before I run HTSeq Count?
Also, HTSeq Count does not appear to be counting singletons. Is there a way to change that?
I have been using HTSeq Count v0.5.3 and I am bit confused about how the stranded options work. I have used both -s no and -s yes and for a few genes the number in the stranded set are higher than in the non-stranded set (and I haven't changed anything else). Looking in the genome browser, I think this is because in -s yes mode those reads for which the mate maps to a different gene or maps ambiguously are counted, whereas -s no ignores these. My data is stranded, so I want to use the stranded mode, but if that means that I am including reads where the mates map improperly, am I better off excluding these from the data before I run HTSeq Count?
Also, HTSeq Count does not appear to be counting singletons. Is there a way to change that?
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