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Cancer Genome Project Exome Sequencing

Agilent whole exome hybridisation capture was performed on genomic DNA derived from cancer and matched normal DNA from the same patients. Next Generation sequencing performed on the resulting exome libraries and mapped to build 37 of the human reference genome to facilitate the identification of novel cancer genes. Now we aim to re find and validate the findings of those exome libraries using bespoke pulldown methods and sequencing the products.

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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
EGAS00001000301 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
EGAF00000133249 bam 5.3 GB
EGAF00000133250 bam 7.6 GB
EGAF00000133251 bam 7.9 GB
EGAF00000133252 bam 7.8 GB
EGAF00000133253 bam 7.9 GB
EGAF00000133254 bam 4.4 GB
EGAF00000149941 bam 5.3 GB
EGAF00000149942 bam 3.2 GB
EGAF00000149943 bam 4.4 GB
EGAF00000149944 bam 9.5 GB
EGAF00000149945 bam 5.5 GB
EGAF00000149946 bam 5.1 GB
12 Files (74.1 GB)