On Tue, May 24, 2011 at 12:40 AM, Aaron Jex wrote:
> Hi,
>
> Can’t seem to find an answer to this on your wiki site and it’s not in the
> tutorial. I would like to filter my 454 reads for high quality regions,
> rename the resulting sequence fragments AND relink the new reads (fragments)
> to the
Hello all,
The 2011 Galaxy Community Conference starts in about 10 hours with the sold
out Introduction to Galaxy session, and then gets fully rolling Wednesday
morning with the main meeting. See the schedule (
http://galaxy.psu.edu/gcc2011/Programme.html) for full details.
If you want to follow
Aaron,
Please do check for contaminants our experience with service providers and
QCI can write a book probably :(. The FastQC suite is a good place to start
(also a galaxy wrapper is available for that). Even for 454 (not having fixed
base positions and fixed lengths) it's quite informa
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