| Literature DB >> 31138589 |
Catherine B Meador1, Geoffrey R Oxnard2,3.
Abstract
Precision cancer medicine requires effective genotyping of every patient's tumor to optimally design treatment plans. Despite its imperfect sensitivity, the rapidity and convenience of cell-free DNA sequencing makes it an essential complement to tumor genotyping, which, when used appropriately, can aid the pursuit of effective genotyping for all patients.See related article by Leighl et al., p. 4691. ©2019 American Association for Cancer Research.Entities:
Mesh:
Year: 2019 PMID: 31138589 PMCID: PMC6679798 DOI: 10.1158/1078-0432.CCR-19-1233
Source DB: PubMed Journal: Clin Cancer Res ISSN: 1078-0432 Impact factor: 12.531