Platform: Hiseq 2000
Data: RNA-Seq
Alignment: TopHat
I want to get regions covered by reads from the tophat-aligned result (accepted_hits.bam).
Is there any way for doing that?
Data: RNA-Seq
Alignment: TopHat
I want to get regions covered by reads from the tophat-aligned result (accepted_hits.bam).
Is there any way for doing that?
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