I am using Galaxy main site to analyse MiSeq data of pooled samples.
Essentially the run produces 3 fastq files consisting of R1, R2 read files and
a separate index file. They are in the format below.
R1: @M00132:6:0-A0JG4:1:1:18014:1842 1:N:0:0
]
Verzonden: maandag 27 februari 2012 19:45
To: 'galaxy-u...@bx.psu.edu'
Onderwerp: [galaxy-user] demultiplex Miseq data with separate index file.
I am using Galaxy main site to analyse MiSeq data of pooled samples.
Essentially the run produces 3 fastq files consisting of R1, R2 read files
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