Discovery and reporting of clinically-relevant germline variants in advanced cancer patients assessed using whole-exome sequencing Running title: Incidental germline variants uncovered during tumor whole-exome sequencing
نویسندگان
چکیده
Tuo Zhang, PhD, Alessandro Romanel, PhD, Kenneth W. Eng, BS, Hanna Rennert, PhD, Adrian Y. Tan, PhD, Yaohua Xue, BA, Joanna Cyrta, MD, Juan Miguel Mosquera, MD, PhD, Andrea Sboner, PhD, Ivan Iossifov ,PhD, Steven M. Lipkin, MD, PhD, Jenny Xiang, MD, Xiaojun Feng, BA, Peter Nelson, MD, Himisha Beltran, MD, Colin C. Pritchard, MD, PhD, Mark A. Rubin, MD, Francesca Demichelis, PhD, and Olivier Elemento, PhD
منابع مشابه
Development and Validation of Clinical Whole-Exome and Whole-Genome Sequencing for Detection of Germline Variants in Inherited Disease.
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