Breast Cancer Exome Resequencing

Study ID Alternative Stable ID Type
EGAS00001000207 Cancer Genomics

Study Description

Agilent whole exome hybridisation capture was performed on genomic DNA derived from Chondrosarcoma 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.

Study Datasets 1 dataset.

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID Description Technology Samples
Breast Cancer Exome Resequencing
Illumina Genome Analyzer II 21

Who archives the data?

There are no publications available