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