
Abstract 1183: Targeted sequencing of cell-free DNA data enables comprehensive profiling of tumor copy number landscape from blood
Author(s) -
Cátálin Bárbácioru,
Eric A. Collisson,
Darya Chudova,
Justin I. Odegaard,
Richard B. Lanman,
AmirAli Talasaz
Publication year - 2018
Publication title -
cancer research
Language(s) - English
Resource type - Conference proceedings
eISSN - 1538-7445
pISSN - 0008-5472
DOI - 10.1158/1538-7445.am2018-1183
Subject(s) - copy number variation , biology , loss of heterozygosity , copy number analysis , computational biology , concordance , deep sequencing , germline , dna sequencing , somatic cell , genome , genetics , exome sequencing , genomics , single cell sequencing , fluorescence in situ hybridization , allele , gene , chromosome , mutation