Utilization of NGS to Identify Mutations in cfDNA: Meet the NGS Experts Series Part 3
Pancreatic cancer is a uniquely lethal malignancy characterized by frequent mutations in KRAS, CDKN2A, SMAD4, TP53 and many others. We have shown that KRAS mutation can be detected in cell-free, circulating tumor DNA (ctDNA) isolated from the plasma in a subset of patients and is associated with poor prognosis. The ability to simultaneously detect multiple pancreatic cancer-specific mutations in ctDNA would open a new avenue for detection of clinically-relevant mutations. In this study, we performed ultra-deep sequencing of ctDNA from advanced pancreatic cancer patients prior to treatment with Gemcitabine and Erlotinib following target enrichment. Somatic, non-synonymous variants were identified in 29 different genes at allele frequencies typically less than 0.5%. Updated results of ultra-deep NGS analysis will be presented.
Видео Utilization of NGS to Identify Mutations in cfDNA: Meet the NGS Experts Series Part 3 канала QIAGEN
Видео Utilization of NGS to Identify Mutations in cfDNA: Meet the NGS Experts Series Part 3 канала QIAGEN
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