ictor
From: Jeremy Goecks [jeremy.goe...@emory.edu]
Sent: Thursday, February 09, 2012 4:00 AM
To: Li, Jilong (MU-Student)
Cc: galaxy-user@lists.bx.psu.edu
Subject: Re: [galaxy-user] How to get reads counts from cufflins?
Victor,
I got the normalized values (FPKM)
Hi all,
I got the normalized values (FPKM) from cufflinks. And I want to get relative
reads counts. How can I do that?
Another question: how does cufflinks handle isoform genes while calculating the
reads counts? Or what papers can help me understand this?
Thank you very much!
Victor
Hi all,
I used TopHat to map RNA-Seq reads to genomes. In the output (.sam) file, the
value of some mapping quality (the 5th column) is 255. What does it mean? And I
found these reads which have mapping quality 255 mapped to unique place.
Thanks!
Victor
Hi,
I want to use cufflinks handle the results of Tophat. Cufflinks uses FPKM to
normalize the expression data. I think FPKM is for pair-end reads. right? My
reads are single-end. Is it right if I use FPKM?
Thank you very much!
Victor
___
From: Jennifer Jackson [j...@bx.psu.edu]
Sent: Thursday, October 27, 2011 11:23 PM
To: Li, Jilong (MU-Student)
Cc: galaxy-u...@bx.psu.edu
Subject: Re: [galaxy-user] how to transfer gene id into protein id
Hello,
If the reference genome is in UCSC and has a RefSeq track, then you can
extract a
Hi,
I have some refseq gene id, like NM_*.
How can I transfer these gene id into protein id, like NP_?
Thank you very much!
Victor
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The Galaxy User list should be used for the discussion of
Galaxy analysis and other features on
Hi,
When I installed galaxy, one error message appeared, which said that
ImportError: No module named distutils.util
Fetch failed.
Could you tell me how to solve this problem?
Thank you very much!
___
The Galaxy User list should be used for
Hi,
When I installed galaxy, one error message appeared, which said that
ImportError: No module named distutils.util
Fetch failed.
Could you tell me how to solve this problem?
Thank you very much!
___
The Galaxy User list should be used for
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