are welcome to post comments/suggestions.
Jen
Galaxy team
On 7/2/12 11:17 AM, Lindsey Kelly wrote:
I am trying to do RNAseq analysis on Paired end data from the Hiseq2000.
I have about 50 files for each sample (25 forward and 25 reverse - although
each sample has a different number of files).
I
I am trying to do RNAseq analysis on Paired end data from the Hiseq2000. I
have about 50 files for each sample (25 forward and 25 reverse - although
each sample has a different number of files).
I think that I need to:
-convert them into FASTQ sanger format using the FASTSQ groomer tool
-check
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