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BASIS_RNAseq

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
EGAD00001001264 Illumina HiSeq 2000 223
EGAD00001001340 Illumina HiSeq 2000 -
EGAD00001001341 Illumina HiSeq 2000 -