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Use of whole-genome sequencing to diagnose a cryptic fusion oncogene.

Authors
  • Welch, John S
  • Westervelt, Peter
  • Ding, Li
  • Larson, David E
  • Klco, Jeffery M
  • Kulkarni, Shashikant
  • Wallis, John
  • Chen, Ken
  • Payton, Jacqueline E
  • Fulton, Robert S
  • Veizer, Joelle
  • Schmidt, Heather
  • Vickery, Tammi L
  • Heath, Sharon
  • Watson, Mark A
  • Tomasson, Michael H
  • Link, Daniel C
  • Graubert, Timothy A
  • DiPersio, John F
  • Mardis, Elaine R
  • And 2 more
Type
Published Article
Journal
JAMA
Publisher
American Medical Association
Publication Date
Apr 20, 2011
Volume
305
Issue
15
Pages
1577–1584
Identifiers
DOI: 10.1001/jama.2011.497
PMID: 21505136
Source
Medline
License
Unknown

Abstract

Whole-genome sequencing can identify cytogenetically invisible oncogenes in a clinically relevant time frame.

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