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Triple_Negative_Breast_Cancer_sequencing

We propose to definitively characterise the somatic genetics of triple-ve breast cancer through generation of comprehensive catalogues of somatic mutations in a number of 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
EGAD00001000063 Illumina Genome Analyzer II 6
EGAD00001000138 Illumina Genome Analyzer II Illumina HiSeq 2000 58
EGAD00001001335 Illumina Genome Analyzer II Illumina HiSeq 2000 28
EGAD00001001338 Illumina Genome Analyzer II Illumina HiSeq 2000 49
EGAD00001002237 Illumina Genome Analyzer II Illumina HiSeq 2000 59
Publications Citations
Pan-cancer landscape of homologous recombination deficiency.
Nat Commun 11: 2020 5584
190