📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites. (2017)

First Author: Long T

Attributed to: A systems based approach to integrating genetic and longitudinal omics data to support diagnosis and prediction of common chronic disease funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/ng.3809

PubMed Identifier: 28263315

Publication URI: http://europepmc.org/abstract/MED/28263315

Type: Journal Article/Review

Volume: 49

Parent Publication: Nature genetics

Issue: 4

ISSN: 1061-4036