21 Mar
2011
21 Mar
'11
3:57 p.m.
On Mon, Mar 21, 2011 at 1:42 PM, David K Crossman <dkcrossm@uab.edu> wrote:
Hello!
I am fairly new to using Galaxy and have a question about the FASTQ Groomer feature. I have 4 RNA-Seq raw data files that were just recently generated from Illumina’s NGS instruments.
Very recently? If they are already using Illumina's CASAVA v1.8 pipeline then the FASTQ files will already be in the Sanger FASTQ format: http://seqanswers.com/forums/showthread.php?t=8895 Peter