Open AccessClinical Interpretation and Implications of Whole-Genome Sequencing
Author(s) -
Frederick E. Dewey,
Megan E. Grove,
Cuiping Pan,
Benjamin A. Goldstein,
Jonathan A. Bernstein,
Hassan Chaı̈b,
Jason D. Merker,
Rachel L. Goldfeder,
Gregory M. Enns,
Sean P. David,
Neda Pakdaman,
Kelly E. Ormond,
Colleen Caleshu,
Kerry Kingham,
Teri E. Klein,
Michelle WhirlCarrillo,
Kenneth Sakamoto,
Matthew T. Wheeler,
Atul J. Butte,
James M. Ford,
Linda M. Boxer,
John P. A. Ioannidis,
Alan C. Yeung,
Russ B. Altman,
Themistocles L. Assimes,
M Snyder,
Euan A. Ashley,
Thomas Quertermous
Publication year - 2014
Publication title -
jama
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.688
H-Index - 680
eISSN - 1538-3598
pISSN - 0098-7484
DOI - 10.1001/jama.2014.1717
Subject(s) - concordance , medicine , pharmacogenomics , genetic testing , whole genome sequencing , disease , medical genetics , genetics , single nucleotide polymorphism , bioinformatics , genotype , genome , gene , biology , pharmacology
Whole-genome sequencing (WGS) is increasingly applied in clinical medicine and is expected to uncover clinically significant findings regardless of sequencing indication.
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