variant calling based on ab1 file from Sanger sequencing
Hi all,
We have use Sanger to verify the variants that are discovered by NGS platform.
Since there are lots of such issues, it is hard for us to look for these variants manually one by one.
Is there any tool that can automatically generate the variant calling results based on ab1 file only?
PS, I've tried novoSNP, but it does not work after loading ref and runs.
Thanks.
Junfeng
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Hello J.F.Jiang!
Questions similar to yours can already be found at:
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Cheers!
PS: Please see other answers on this site - other people clearly have got novoSNP running.