Use of whole-genome sequencing to diagnose a cryptic fusion oncogene.
Welch JS, Westervelt P, Ding L, Larson DE, Klco JM, Kulkarni S, Wallis J, Chen K, Payton JE, Fulton RS, Veizer J, Schmidt H, Vickery TL, Heath S, Watson MA, Tomasson MH, Link DC, Graubert TA, DiPersio JF, Mardis ER, Ley TJ, Wilson RK
Department of Medicine, Washington University, St Louis, Missouri, USA.
Published 20 April 2011 in JAMA, 305(15): 1577-84.
Full-text of this article is available online (may require subscription).
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[Abstract] [Full-text]
Use of whole-genome sequencing to diagnose a cryptic fusion oncogene. JAMA, 305(15): 1577-84.
[Abstract] [Full-text]
Identification of a novel TP53 cancer susceptibility mutation through whole-genome sequencing of a patient with therapy-related AML. JAMA, 305(15): 1568-76.
[Abstract] [Full-text]
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