Radboudumc Cancer Genomics DAC

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Dataset ID	Description	Technology	Samples
EGAD00001004534	Whole exome sequencing of 17 tumors from 12 different individuals with biallelic germline NTHL1 mutations from 9 different tissue types. Provided are 17 bam files which are mapped to human genome version GRCh37.	Illumina HiSeq 4000 NextSeq 500	17
EGAD50000000112	WES data of 17 tumors from 9 individuals that have biallelic germline CHEK2 pathogenic variants. Shallow whole genome sequencing files from 16 tumors samples from 9 individuals with germline biallleic pathogenic variants in CHEK2.	Illumina NovaSeq 6000	17
EGAD50000000113	Whole exome sequencing data from the tumors of individuals with constitutional mismatch repair deficiency. These are 16 tumors from the bigger study of 41 tumors in total (from 17 individuals in total).	Illumina NovaSeq 6000	16