Triple Negative Breast Cancer Whole Genome Validations
|Study ID||Alternative Stable ID||Type|
Study Datasets 1 dataset.
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We propose to definitively characterise the somatic genetics of Triple negative breast cancer through generation of comprehensive catalogues of somatic mutations in 500 cases by high coverage genome sequencing coupled with integrated transcriptomic and methylation analyses. This study will use a bespoke bait set to pulldown regions of interest found in whole genome sequencing to validate mutations found.
|Illumina HiSeq 2000||46|