Phasing for medical sequencing using rare variants and large haplotype reference panels. (2016)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/bioinformatics/btw065
PubMed Identifier: 27153703
Publication URI: http://europepmc.org/abstract/MED/27153703
Type: Journal Article/Review
Volume: 32
Parent Publication: Bioinformatics (Oxford, England)
Issue: 13
ISSN: 1367-4803