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[Seqan-dev] Rabema and RazerS3

<-- thread -->
<-- date -->
  • From: Uwe Appelt <uappelt@clcbio.com>
  • To: seqan-dev@lists.fu-berlin.de
  • Date: Tue, 28 Aug 2012 09:31:05 +0200
  • Reply-to: SeqAn Development <seqan-dev@lists.fu-berlin.de>
  • Subject: [Seqan-dev] Rabema and RazerS3

Hi @All.

Liking Rabema, I appreciated the release of RazerS3 and the updates to the Rabema-manual (on http://www.seqan.de/projects/rabema/manual/).

Q1) So to produce a golden standard we would execute the following command (as given in step 1A):

razers3 -v -of sam -rr 100 -i 92 -m 1000000 -ds -o gold_pre.sam genome.fa reads.fq

This is however imprecisely updated, because the "-ds" option does seem to exist in razers3 ("razers3: illegal option --ds"). I assume, I can just omit the "-ds"?

Q2) In step 1b, postprocessing of the razers3-sam output is described, does that still apply?

Q3) Just a minor thing: in step (1A) you use an identity value of 92%, while you describe 6% to be the corresponding error rate in step (2). That's just a typo, I guess?!

Thanks in advance,
Uwe




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    • Re: [Seqan-dev] Rabema and RazerS3
      • From: "Holtgrewe, Manuel" <manuel.holtgrewe@fu-berlin.de>
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