“CLINICAL BINNING” of patient genomic variant data for the medical staff at UNC-Chapel Hill. “This assigns a clinical relevancy to every one of the variants, allowing clinicians and patients to determine the types of variants they care about. Once variants are binned, we have a web site that delivers the information on the individual to his or her physicians.” Processing just 30 genomes a week needs 200-300 terabytes of genomic data on the computer. ”
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