Whole genome sequencing identifies rare genetic variants in familial pancreatic cancer patients

Ming Tan*, Klaus Brusgaard, Anne-Marie Gerdes, Martin Jakob Larsen, Michael Bau Mortensen, Sönke Detlefsen, Ove B Schaffalitzky de Muckadell, Maiken Thyregod Joergensen

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

116 Downloads (Pure)
Original languageEnglish
JournalAnnals of Human Genetics
Volume86
Issue number4
Pages (from-to)195-206
ISSN0003-4800
DOIs
Publication statusPublished - Jul 2022

Keywords

  • familial pancreatic cancers
  • pancreatic ductal adenocarcinoma
  • protein truncating variants
  • rare variants
  • whole genome sequencing
  • Genetic Predisposition to Disease
  • Carcinoma
  • Humans
  • Pancreatic Neoplasms/genetics
  • Whole Genome Sequencing

Cite this