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Old 08-27-2014, 06:18 PM   #1
stormin
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Location: US

Join Date: Aug 2014
Posts: 23
Default Illumina HiSeq2500 data

I am trying to determine the method used to generate my RNAseq data. On the Illumina website, the read length are either 1*36bp or 2*50bp. My fastq reads are non-strand-specific and non-paired sequences of 50bp each. I'm not sure how to interpret this...
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