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.

Advertisements

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s