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. Click on one of the Study IDs below to find out more.

Study ID Study Title Study Type
EGAS00001000301 Other
ID File Type Size Located in Quality Control
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
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