Germline WES of serrated polyposis syndrome
The serrated polyposis syndrome (SPS) is a disease with a mainly unknown inherited genetic basis characterized by the presence of multiple and/or large serrated polyps in the colon and a higher associated risk for colorectal cancer (CRC). The objective of the present study was to identify new SPS/CRC germline predisposition genes by using whole-exome sequencing in two affected SPS patients from the same family.
- Type: Exome Sequencing
- Archiver: European Genome-Phenome Archive (EGA)
Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data
| Dataset ID | Description | Technology | Samples |
|---|---|---|---|
| EGAD50000001126 | Illumina HiSeq 2000 | 2 |
| Publications | Citations |
|---|---|
|
Germline and Somatic Whole-Exome Sequencing Identifies New Candidate Genes Involved in Familial Predisposition to Serrated Polyposis Syndrome.
Cancers (Basel) 13: 2021 929 |
20 |
|
Germline pathogenic variants in HIC1 DNA binding domains are associated with familial serrated polyposis syndrome.
Int J Cancer 157: 2025 1154-1167 |
1 |
