Cancer and germline exomes consisting of FASTQ reads from melanoma, lung and colon cancer samples
Cancer and germline exomes consisting of FASTQ reads from 6 individuals (4 melanoma, 1 lung and 1 colon cancer). Exome sequencing was performed on illumina with a depth of 100x to 200x. 2 Melanoma datasets contain reads from 2 different tumor regions 2 Melanoma datasets contain reads from 1 tumor region and from a tumor derived cell line 1 Melanoma dataset contains reads from 2 healthy tissues Colon and lung datasets contain both 1 matched germline-tumor pair
- 17 samples
- DAC: EGAC00001002246
- Technology: Illumina HiSeq 4000
CHUV DAC
It is required that users obtain authorization from the CHUV for accessing the controlled data. Any user requesting access to the controlled data must apply for authorization and sign a Data Transfer and Use Agreement, which is granted by the Data Access Committee (DAC). DACs review and approve or disapprove all requests from the research community for data access. Decisions to grant access are made based on whether the request conforms to program specific requirements or procedures. Any user accessing the above data must adhere to a Data Transfer and Use Agreement.
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 |
---|---|---|
EGAS00001005513 | 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.