gDNA enrichment by a transposase-based technology for NGS analysis of the whole sequence of BRCA1, BRCA2, and 9 genes involved in DNA damage repair

J Vis Exp. 2014 Oct 6:(92):e51902. doi: 10.3791/51902.

Abstract

The widespread use of Next Generation Sequencing has opened up new avenues for cancer research and diagnosis. NGS will bring huge amounts of new data on cancer, and especially cancer genetics. Current knowledge and future discoveries will make it necessary to study a huge number of genes that could be involved in a genetic predisposition to cancer. In this regard, we developed a Nextera design to study 11 complete genes involved in DNA damage repair. This protocol was developed to safely study 11 genes (ATM, BARD1, BRCA1, BRCA2, BRIP1, CHEK2, PALB2, RAD50, RAD51C, RAD80, and TP53) from promoter to 3'-UTR in 24 patients simultaneously. This protocol, based on transposase technology and gDNA enrichment, gives a great advantage in terms of time for the genetic diagnosis thanks to sample multiplexing. This protocol can be safely used with blood gDNA.

Publication types

  • Research Support, Non-U.S. Gov't
  • Video-Audio Media

MeSH terms

  • Base Sequence
  • Breast Neoplasms / genetics*
  • DNA / chemistry
  • DNA / genetics*
  • DNA Damage / genetics*
  • DNA Repair / genetics*
  • Female
  • Genes, BRCA1*
  • Genes, BRCA2*
  • Genome, Human
  • Humans
  • Molecular Sequence Data
  • Sequence Analysis, DNA / methods*
  • Transposases / chemistry
  • Transposases / genetics*

Substances

  • DNA
  • Transposases