MSV: a modular structural variant caller that reveals nested and complex rearrangements by unifying breakends inferred directly from reads

Genome Biol. 2023 Jul 17;24(1):170. doi: 10.1186/s13059-023-03009-5.

Abstract

Structural variant (SV) calling belongs to the standard tools of modern bioinformatics for identifying and describing alterations in genomes. Initially, this work presents several complex genomic rearrangements that reveal conceptual ambiguities inherent to the representation via basic SV. We contextualize these ambiguities theoretically as well as practically and propose a graph-based approach for resolving them. For various yeast genomes, we practically compute adjacency matrices of our graph model and demonstrate that they provide highly accurate descriptions of one genome in terms of another. An open-source prototype implementation of our approach is available under the MIT license at https://github.com/ITBE-Lab/MA .

Keywords: Alignment; Ambiguity; Complex SV; MEMs; Nested SV; Pan-genomes; Seeds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Computational Biology
  • Genome
  • Genomics*
  • High-Throughput Nucleotide Sequencing
  • Sequence Analysis, DNA
  • Software*