Mutation detection for cancer screening and fetal analysis

摘要

Problem to be solved: to provide a new technique for the non invasive implementation of extensive screening, detection, or evaluation for cancer.Problem to be solved: to provide an accurate detection of somatic mutations in a plasma patient (or other samples containing anoxic DNA) that are being screened for cancer patients and cancers. Detection of these molecular markers is useful for screening, detection, monitoring, management and prognostic diagnosis of cancer patients.No selection