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Rare germline variants in patients with personal and family history of colorectal cancer

A double primary colorectal cancer (CRC) in a familial setting signals a high risk of CRC. In order to find novel high/moderate penetrance CRC susceptibility genes, we performed whole-exome sequencing on germline blood samples of seven familial cases from Poland with a double primary CRC.

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Studies are experimental investigations of a particular phenomenon, e.g., case-control studies on a particular trait or cancer research projects reporting matching cancer normal genomes from patients.

Study ID Study Title Study Type
EGAS50000000606 Exome Sequencing

This table displays only public information pertaining to the files in the dataset. If you wish to access this dataset, please submit a request. If you already have access to these data files, please consult the download documentation.

ID File Type Size Quality Report
Located in
EGAF50000199964 bam 8.5 GB Report
EGAF50000199965 bam 8.6 GB Report
EGAF50000199966 bam 8.4 GB Report
EGAF50000199967 bam 8.8 GB Report
EGAF50000199968 bam 8.3 GB Report
EGAF50000199969 bam 8.6 GB Report
EGAF50000199970 bam 8.7 GB Report
7 Files (59.9 GB)