Phenomics and the interpretation of personal genomes

Slavé Petrovski; David B Goldstein

doi:10.1126/scitranslmed.3010272

Phenomics and the interpretation of personal genomes

Sci Transl Med. 2014 Sep 17;6(254):254fs35. doi: 10.1126/scitranslmed.3010272.

Authors

Slavé Petrovski¹, David B Goldstein²

Affiliations

¹ Center for Human Genome Variation, Duke University School of Medicine, Durham, NC, 27708, USA. Department of Medicine, The University of Melbourne, Austin Health and Royal Melbourne Hospital, Melbourne, Victoria 3050, Australia. slave.petrovski@duke.edu d.goldstein@duke.edu.
² Center for Human Genome Variation, Duke University School of Medicine, Durham, NC, 27708, USA. slave.petrovski@duke.edu d.goldstein@duke.edu.

PMID: 25232173
DOI: 10.1126/scitranslmed.3010272

Abstract

In contemporary genomics research, phenotype-driven bioinformatics approaches hint at the potential of establishing a framework for quantifying phenotypic similarities among patients (Zemojtel et al., issue 252).

MeSH terms

Genome, Human*
Humans
Phenotype
Precision Medicine*