Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications. (2014)

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ng.3036

PubMed Identifier: 25017105

Publication URI: http://europepmc.org/abstract/MED/25017105

Type: Journal Article/Review

Volume: 46

Parent Publication: Nature genetics

Issue: 8

ISSN: 1061-4036