Rapid Detection of Rare Deleterious Variants by Next Generation Sequencing with Optional Microarray SNP Genotype Data. (2015)

First Author: Watson CM
Attributed to:  Infrastructure for collaboration: Leeds MRC Medical Bioinformatics Centre funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/humu.22818

PubMed Identifier: 26037133

Publication URI: http://europepmc.org/abstract/MED/26037133

Type: Journal Article/Review

Volume: 36

Parent Publication: Human mutation

Issue: 9

ISSN: 1059-7794