Group-based Variant Calling

[PMID: 26395405] [BMC Bioinformatics]

Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies

437 whole human genomes sequenced to ~35× coverage. Group calling leverages reads obtained from more than a single individual’s genome in order to make more confident claims about the presence of a variant allele in any single genome. Gordon supercomputer cluster @ San Diego Supercomputer Center.


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