[Seqan-dev] SNP and Indel location

From: Anantharamanan R <ananthr@ncbs.res.in>
To: seqan-dev@lists.fu-berlin.de
Date: Fri, 13 Apr 2012 15:51:59 +0530
Reply-to: SeqAn Development <seqan-dev@lists.fu-berlin.de>
Subject: [Seqan-dev] SNP and Indel location

Dear All,

I am simulating illumina reads with -hs, -hi (default rate 0.001). I want to know where exactly these variants are introduced (Location) into my genome during simulation. It would be really great if somebody help me to trace this.

Regards
Ananth

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- Re: [Seqan-dev] SNP and Indel location
  - From: "Holtgrewe, Manuel" <manuel.holtgrewe@fu-berlin.de>

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