Using Genome-Wide Linkage Analysis and Next Generation Sequencing Approaches to Identify the Genes Responsible for the Familial Colorectal Cancer Type X

Project: A - Government Institution › b - National Science and Technology Council

Project Details

StatusFinished
Effective start/end date8/1/17 → 7/31/18

Keywords

  • copy number variation (CNV)
  • familial CRC type X (FCCX)
  • genome-wide linkage analysis
  • hereditary non-polyposis colorectal cancer (HNPCC)
  • rare variant
  • whole exome sequencing (WES)

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