[mira_talk] Re: paired_end
- From: Bastien Chevreux <bach@xxxxxxxxxxxx>
- To: mira_talk@xxxxxxxxxxxxx
- Date: Tue, 14 Apr 2009 23:36:56 +0200
On Tuesday 14 April 2009 Lionel Guy wrote:
> On 14 Apr 2009, at 16:08 , Jan Paces wrote:
> > Unfortunately it looks like it
> > is not possible to download .sff files from NCBI trace archive
> > anymore,
> > they are offering only fasta or fastq
It's not anymore? Oh hell, that would be a shame. Need to check that.
> I think there are some other utilities in the third-party tools of
> mira, although I don't know how they work. AFAIK, I have split my
> reads, using .r and .f suffixes. The xml file then resembles:
Yep, that's what it looks like. Ideally suited if you have multiple library
sizes.
If you happen to have only *one* library size per sequencing technology, you
can still use -GE:tismin and -GE:tismax.
E.g. to set up library size of 10k+/-3k for Sanger and 3k+/-1k for 454:
mira ... --job=...,sanger,454
-GE:tismin=7000:tismax=13000
-454_SETTINGS
-GE:tismin=2000:tismax=4000
Regards,
Bastien
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