Analytical and Clinical Validation of a Digital Sequencing Panel for Quantitative, Highly Accurate Evaluation of Cell-Free Circulating Tumor DNA.

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Published in PLoS One on October 16, 2015

Authors

Richard B Lanman1, Stefanie A Mortimer2, Oliver A Zill2, Dragan Sebisanovic2, Rene Lopez2, Sibel Blau3, Eric A Collisson4, Stephen G Divers5, Dave S B Hoon6, E Scott Kopetz7, Jeeyun Lee8, Petros G Nikolinakos9, Arthur M Baca1, Bahram G Kermani2, Helmy Eltoukhy10, AmirAli Talasaz11

Author Affiliations

1: Department of Medical Affairs, Guardant Health, Inc., Redwood City, California, United States of America.
2: Department of Research and Bioinformatics, Guardant Health, Inc., Redwood City, California, United States of America.
3: Rainier Hematology Oncology, Northwest Medical Specialties, Puyallup, Washington, United States of America.
4: Department of Medicine, University of California San Francisco School of Medicine, San Francisco, California, United States of America.
5: Genesis Cancer Center, Hot Springs, Arkansas, United States of America.
6: Department of Molecular Oncology, John Wayne Cancer Institute at Saint John's Health Center, Santa Monica, California, United States of America.
7: Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
8: Department of Medicine, Division of Hematology-Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
9: Department of Hematology and Medical Oncology, University Cancer and Blood Center, Athens, Georgia, United States of America.
10: Administration, Guardant Health, Inc., Redwood City, California, United States of America.
11: Department of Research and Bioinformatics, Guardant Health, Inc., Redwood City, California, United States of America; Administration, Guardant Health, Inc., Redwood City, California, United States of America.

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