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Deep whole genome sequencing identifies recurrent genomic alterations in commonly used breast cancer cell lines and patient-derived xenograft models.

Niantao DengAndre MinocheKate HarveyMeng LiJuliane WinklerAndrei GogaAlexander Swarbrick
Published in: Breast cancer research : BCR (2022)
Our WGS data provides a comprehensive genome sequencing resource of these models.
Keyphrases
  • genome wide
  • electronic health record
  • single cell
  • copy number
  • dna methylation
  • gene expression
  • young adults