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Three large nuclear families in which a single child per family was diagnosed with cancer

We collected saliva samples from three nuclear families having 4, 5, and 7 children, respectively. One child in each nfamily had been diagnosed with a pediatric tumor, and neither parent had been diagnosed with cancer. Diagnoses included Wilms tumor, low-grade astrocytoma, and Burkitt’s lymphoma, respectively. We used whole-genome sequencing to profile normal cells from each family member and a linked-read technology.

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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
EGAS00001005321 Other

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 Located in
EGAF00005302343 bam 79.9 GB
EGAF00005302344 bam 75.3 GB
EGAF00005302345 bam 78.9 GB
EGAF00005302346 bam 91.5 GB
EGAF00005302347 bam 92.5 GB
EGAF00005302348 bam 83.0 GB
EGAF00005302349 bam 98.5 GB
EGAF00005302350 bam 96.3 GB
EGAF00005302351 bam 96.6 GB
EGAF00005302352 bam 94.9 GB
EGAF00005302353 bam 94.9 GB
EGAF00005302354 bam 97.4 GB
EGAF00005302355 bam 101.4 GB
EGAF00005302356 bam 102.6 GB
EGAF00005302357 bam 100.5 GB
EGAF00005302358 bam 102.8 GB
EGAF00005302359 bam 101.6 GB
EGAF00005302360 bam 101.7 GB
EGAF00005302361 bam 100.1 GB
EGAF00005302362 bam 100.4 GB
EGAF00005302363 bam 100.4 GB
EGAF00005302364 bam 99.0 GB
22 Files (2.1 TB)