Genome Sequencing of Familial Cholangiocarcinoma for the Identification of Germline Risk Alleles

In this study, sequencing data (WES, WGS, linked-read WGS) was used to identify candidate causal germline variants in a family with inherited cholangiocarcinoma. Candidate causal SNVs and indels were identified from the germline WES data of eight siblings (four affected, four unaffected), then somatic second hits were identified from matched tumor/normal pairs. Second hits were verified using haplotype information derived from linked-read WGS of the tumor data.

• Type: Parent-Offspring Trios
• Archiver: The database of Genotypes and Phenotypes (dbGaP)