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Targeted Pulldown Validation of mutations found in whole genome sequencing

This experiment is to inform us of the validity of using pre-made library material to perform a bespoke pulldown experiment to validate the mutations found between the whole genome sequencing of the DNA from the same individuals cancer and normal material. This is to identify the valid and informative mutations in cancer genomes.

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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
EGAS00001000260 Cancer Genomics

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
EGAF00000660815 bam 362.4 MB
EGAF00000660816 bam 444.9 MB
EGAF00000660817 bam 341.5 MB
EGAF00000660818 bam 544.3 MB
4 Files (1.7 GB)