Hi Vasu,

Thanks for your response.  I realize tophat and bowtie are different.  But
my question was concerning what seemed to me to be divergent results from
mapping with tophat and bwa (which I also realize are different).  bwa
seemed to map around 4x the reads that tophat mapped using the same
reference.  Should this not come as a surprise?

Austin

On Wed, Apr 27, 2011 at 2:30 PM, vasu punj <pu...@yahoo.com> wrote:

> Though Tophat calls in Bowtie but they are different mapping tools. Details
> can be found in mannual of Tophat. For RNA-seq one may be stick with Tophat.
>
> Vasu
>
> --- On *Wed, 4/27/11, Austin Paul <austi...@usc.edu>* wrote:
>
>
> From: Austin Paul <austi...@usc.edu>
> Subject: [galaxy-user] mapping with tophat vs. bwa
> To: galaxy-user@lists.bx.psu.edu
> Date: Wednesday, April 27, 2011, 4:20 PM
>
>
> Hello,
>
> I am getting what seems to me to be strange results using two different
> mapping tools in Galaxy.  I am mapping illumina RNA-seq data and with
> tophat, while setting # alignments to 1, I get around 15-20% reads mapping.
> And when I use bwa, I am getting around 75% reads mapping.  My reference is
> a collection of ESTs so the strength of tophat being a spliced read mapper
> is probably not being utilized, but I am surprised by the difference in the
> number of reads mapping between the two.  Any thoughts?
>
> Austin
>
> -----Inline Attachment Follows-----
>
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