BreakTrans: uncovering the genomic architecture of gene fusions

Genome Biol. 2013 Aug 23;14(8):R87. doi: 10.1186/gb-2013-14-8-r87.

Abstract

Producing gene fusions through genomic structural rearrangements is a major mechanism for tumor evolution. Therefore, accurately detecting gene fusions and the originating rearrangements is of great importance for personalized cancer diagnosis and targeted therapy. We present a tool, BreakTrans, that systematically maps predicted gene fusions to structural rearrangements. Thus, BreakTrans not only validates both types of predictions, but also provides mechanistic interpretations. BreakTrans effectively validates known fusions and discovers novel events in a breast cancer cell line. Applying BreakTrans to 43 breast cancer samples in The Cancer Genome Atlas identifies 90 genomically validated gene fusions. BreakTrans is available at http://bioinformatics.mdanderson.org/main/BreakTrans.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Atlases as Topic
  • Breast Neoplasms / genetics*
  • Cell Line, Tumor
  • Chromosome Breakpoints*
  • Female
  • Gene Dosage
  • Genome, Human
  • Humans
  • Molecular Sequence Annotation
  • Oncogene Fusion*
  • Oncogene Proteins, Fusion / genetics*
  • Sensitivity and Specificity
  • Software*

Substances

  • Oncogene Proteins, Fusion