Hi all,
what is the difference between using "NGS:mapping---Map with
Bowtie for Illumina" and "NGS: RNA analysis-Tophat for
Illumina" when mapping reads against a reference/custom genome?
thanks,
ib
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The Galaxy User list should
Dear all,
I ran Cuffdiff with 3 groups: A, B, C each with 2, 5 and 1 replicates
respectively.
When looking at the transcripts dif.exp.testing, I have only sample A
and B and redpective values.
What happened to sample C?
Thanks for any help.
ib
_
Sorry, I did not read carefully. All three samples are listed, just
down in the column I found the other sample.
ib
On Sat, Aug 11, 2012 at 7:41 PM, i b wrote:
> Dear all,
> I ran Cuffdiff with 3 groups: A, B, C each with 2, 5 and 1 replicates
> respectively.
> When looking at the transcripts d
I'd like to start an open discussion on the topic of parallelization for
NGS data. I noticed that Galaxy recently came out with a cloud-based
interface using Amazon EC3. I've been trying to learn more about how these
NGS analysis algorithms (for alignment, assemly, etc.) are actually
implemented in
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