作者: M. McCarthy
DOI: 10.1136/BMJ.H2036
关键词:
摘要: Clinicians who rely on genomic analysis of only a patient’s tumor tissue to guide cancer therapy could be misled by the presence harmless mutations that are also present in normal germline cells and unrelated cancer, study published Science Translational Medicine has found.1 Increasingly, it become standard practice perform sequencing identify cancer-causing responsible for development growth. Of particular interest clinicians “actionable genes” whose can help …