rose_is...@yahoo.com ___
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Dear all,
I have a trouble with the Megablast program available in NGS Mapping
and I hope that you can help. Indeed, I think that there might be a
problem with the table given in output, and notably a shift between
the GI numbers and the parameters associated.
Here are the details:
I. First,
Hi,
I used the cufflinks to assemble my SAM file, but the results showed some
CUFF's status in not OK,it's FAIL, so that means these CUFF's corresponding
sequence could not used or else mean? Thanks a lot!
Reards
weimin zhao___
The
Hello Weimin,
The majority of issues user's encounter with RNA-seq tools is related to
the inputs, so troubleshooting format is the first step. Please see the
section Example: unexpected results with RNA-seq analysis tools here:
Hello all,
The January Events http://wiki.g2.bx.psu.edu/Events email is going out a
little early this month, mainly because of a *December 15 deadline for
the Galaxy
Developer Workshop in the Czech
Republichttp://evomics.org/workshops/galaxy-developer-workshop/
*.
There are Galaxy-related events
Hello,
Does anyone know how to get alignment stats from Bowtie on Galaxy? I
would like to know what percentage of total reads from my dataset is
aligned.
I know if you run Bowtie using the command line, it gives you the
report. However, I could not find percent alignment on Galaxy.
Thanks
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