I used bwasw to align my Illumina reads to a reference genome. Then I use Samtool to pileup to an output.
In the output, it only shows hetero or homo on the SNP base. But I also want to see thea ctual sequences of aligned fragments, queried reads and aligned genome fragments.
How do I do it?
In the output, it only shows hetero or homo on the SNP base. But I also want to see thea ctual sequences of aligned fragments, queried reads and aligned genome fragments.
How do I do it?
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