Hi Shakuntala,

One of our engineers also had this to say:

You might want to consider if blat is the appropriate mapping tool for
short reads.  It may work if their reads are long enough, but I
believe the short read community has better aligners for this type of
work.

Vanessa Kirkup Swing
UCSC Genome Bioinformatics Group

On Thu, Jul 21, 2011 at 3:57 PM, Vanessa Kirkup Swing
<[email protected]> wrote:
> Hi Shakuntala,
>
> Please see this BLAT help section:
>
> http://genome.ucsc.edu/goldenPath/help/hgTracksHelp.html#BLATAlign
>
> You will likely want to run BLAT from the command line since it sounds
> like you have your own reference sequence you want to compare to.
>
> Here is more information on the command line version of BLAT:
>
> http://genome.ucsc.edu/goldenPath/help/blatSpec.html
>
> I hope this clarifies things for you. If you have further questions,
> please contact the mailing list.
>
> Vanessa Kirkup Swing
> UCSC Genome Bioinformatics Group
>
>
> ---------- Forwarded message ----------
> From: Fathepure, Shakuntala <[email protected]>
> Date: Wed, Jul 20, 2011 at 7:25 PM
> Subject: [Genome] BLAT
> To: "[email protected]" <[email protected]>
> Cc: "[email protected]" <[email protected]>
>
>
>
> I am trying to use BLAT to blast short reads(FASTQ) from the NCBI, SRA
> with my custom reference sequence(fasta format) to check the hits and
> then design primers. I am bit confused how to use the program
> efficiently. I am planning to read the help to find solutiosn. I would
> really appreciate, if you can help me with the above situation.
>
> Thank you,
> Shakuntala Fathepure
> Postdoc
> Dept. of Botany
> Oklahoma State University
> Stillwater, OK 74078
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> Genome maillist  -  [email protected]
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>

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