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Breast_Cancer_Whole_Genome_Sequencing

We propose to definitively characterise the somatic genetics of ER+ve, HER2-ve 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.

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
EGAD00001000121 Illumina HiSeq 2000 6
EGAD00001001338 Illumina Genome Analyzer II Illumina HiSeq 2000 -