Description: The SK-BR-3 cell line is one of the most important models for HER2+ breast cancers, which affect one in five breast cancer patients. SK-BR-3 is known to be highly rearranged although much of the variation is in complex and repetitive regions that may be underreported. Addressing this, we sequenced SK-BR-3 using long-read single molecule sequencing from Pacific Biosciences, and develop one of the most detailed maps of structural variations (SVs) in a cancer genome available with nearly 20,000 variants present, most of which were missed by short read sequencing. Full-length IsoSeq transcriptome sequencing further revealed several novel gene fusions within the nested genomic variants.

Data type: raw sequence reads

Sample scope: Multispecies

Relevance: Medical

Last updated: 2018-06-15