Authors
Chaohui Li, Siavash Raeisi Dehkordi, Daniel Muliaditan, Ramanuj DasGupta, Jens Luebeck, Kaiyuan Zhu, Vineet Bafna
Published in
Bioinformatics (Oxford, England). Volume 42. Issue Supplement_1. Jul 01, 2026.
Abstract
Focal oncogene amplification is a key driver of tumor progression. Remarkably, the increased pathology depends on the context-whether the amplification is extrachromosomal (ecDNA) or intrachromosomal. EcDNA amplifications promote heterogeneity, therapy resistance, and poor prognosis. Focal intrachromosomal amplifications often arise through breakage-fusion-bridge (BFB) cycles, which produce highly rearranged but stable chromosomes. Distinguishing BFB from ecDNA remains challenging due to overlapping genomic signatures. To address this, we present BFBArchitect, a computational method leveraging long-read Oxford Nanopore data to identify BFB sequences consistent with both copy number and structural variations.
We provide a novel combinatorial characterization of BFB, which naturally leads to an integer linear programming (ILP) optimization. The ILP optimization generates a BFB sequence that best explains experimentally observed copy numbers and foldback structural variants. We implement this idea in a tool called BFBArchitect, which achieves near-perfect accuracy in distinguishing BFB from non-BFB structures in extensive simulations as well as on 18 validated tumor samples. Moreover, it generates sequence-level BFB reconstructions that provide mechanistic insights into BFB formation, including repair mechanisms with template switching and other structural variants, and recapture of telomere for stabilization.
BFBArchitect is available at https://github.com/AmpliconSuite/BFBArchitect.
PMID:
42412795
Bibliographic data and abstract were imported from PubMed on 08 Jul 2026.
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