Personalized genomic analyses for cancer mutation discovery and interpretation.

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🔗 View Article (PMC 4442685)

Published in Sci Transl Med on April 15, 2015

Authors

Siân Jones1, Valsamo Anagnostou2, Karli Lytle1, Sonya Parpart-Li1, Monica Nesselbush1, David R Riley1, Manish Shukla1, Bryan Chesnick1, Maura Kadan1, Eniko Papp2, Kevin G Galens1, Derek Murphy1, Theresa Zhang1, Lisa Kann1, Mark Sausen1, Samuel V Angiuoli1, Luis A Diaz2, Victor E Velculescu3

Author Affiliations

1: Personal Genome Diagnostics, Baltimore, MD 21224, USA.
2: The Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.
3: The Sidney Kimmel Comprehensive Cancer Center, The Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA. velculescu@jhmi.edu.

Associated clinical trials:

MED-C Registry: Advanced Malignancy or Myelodysplasia, Tested by Standard Sequencing and Treated by Physician Choice (N1) | NCT02900248

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