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