These are Illumina reads

-S.

On Tue, Mar 29, 2011 at 11:37 AM, Anton Nekrutenko <anton@bx.psu.edu> wrote:

Are these illumina or solid reads?

Tx,

anton

On Mar 29, 2011, at 11:29 AM, Surya Saha wrote:

> Hi,
>
> I have two fastq files with the forward(/1) and reverse(/2) paired reads. The reads are not in same order in either file, some pairs are absent/missing and the files are 8 GB each with abt 30 mill reads each.
>
> I am trying to pull out all the paired reads for which both fwd and rev exist. Can I use a combination of fastq tools in Galaxy to do this?
>
> Thanks!
>

> -Surya ___________________________________________________________
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Anton Nekrutenko
http://nekrut.bx.psu.edu
http://usegalaxy.org