Entering edit mode
11.7 years ago
Honey
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200
I have a data from Hi-seq for a bacterial RNA-seq , however, it is an over kill, with any aligner it gives ma around >1GB data no mismatch. What may be the best strategy to analyze such data? I think if I take a fraction of the data that may be useful but I dont know how I can take fraction of aligned reads from Bam file? Any suggestion please?
Sorry, I don't understand the question. Can you clarify what you mean by "around >1GB data no mismatch"?
Agree with Mikael, please clarify.