Breast_Cancer_Exome_Sequencing
Agilent whole exome hybridisation capture will be performed on genomic DNA derived from 100 breast cancers of all subtypes and matched normal DNA from the same patients. Three lanes of Illumina GA sequencing will be performed on the resulting 200 exome libraries and mapped to build 37 of the human reference genome to facilitate the identification of novel cancer genes.
- Type: Cancer Genomics
- Archiver: European Genome-Phenome Archive (EGA)
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 |
---|---|---|---|
EGAD00001000110 | Illumina Genome Analyzer II Illumina HiSeq 2000 | 179 | |
EGAD00001000133 | Illumina Genome Analyzer II Illumina HiSeq 2000 | 199 | |
EGAD00001000637 | Illumina Genome Analyzer II Illumina HiSeq 2000 | 4 | |
EGAD00001002697 | Illumina HiSeq 2000 | 9 |
Publications | Citations |
---|---|
Genomic Evolution of Breast Cancer Metastasis and Relapse.
Cancer Cell 32: 2017 169-184.e7 |
363 |