Study

ER HER2 PR breast Cancer genome sequencing

Study ID Alternative Stable ID Type
EGAS00001000197 Cancer Genomics

Study Description

Agilent whole exome hybridisation capture will be performed on genomic DNA derived from X triple negative breast cancers and matched normal DNA from the same patients. Three lanes of Illumina GA sequencing will be performed on the resulting X exome libraries and mapped to build 37 of the human reference genome to facilitate the identification of novel cancer genes.

Study Datasets 2 datasets.

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
EGAD00001000088
ER-, HER2-, PR- breast Cancer genome sequencing
Illumina Genome Analyzer II 6
EGAD00001000133
The landscape of cancer genes and mutational processes in breast cancer
Illumina Genome Analyzer II,Illumina HiSeq 2000 199

Who archives the data?

There are no publications available