Integrating 400 million variants from 80,000 human samples with extensive annotations: towards a knowledge base to analyze disease cohorts. (2016)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1186/s12859-015-0865-9
PubMed Identifier: 26746786
Publication URI: http://europepmc.org/abstract/MED/26746786
Type: Journal Article/Review
Volume: 17
Parent Publication: BMC bioinformatics
ISSN: 1471-2105