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Old 09-04-2014, 05:37 AM   #2
Devon Ryan
Location: Freiburg, Germany

Join Date: Jul 2011
Posts: 3,480

Dealing with large numbers of fastq or BAM files would take a while, so I'd just look at 1000 genomes and TCGA datasets. You should be able to just look for the variant that way without needing to do SNP calling or alignment.
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