rMFilter: acceleration of long read-based structure variation calling by chimeric read filtering

Bioinformatics. 2017 Sep 1;33(17):2750-2752. doi: 10.1093/bioinformatics/btx279.

Abstract

Motivation: Long read sequencing technologies provide new opportunities to investigate genome structural variations (SVs) more accurately. However, the state-of-the-art SV calling pipelines are computational intensive and the applications of long reads are restricted.

Results: We propose a local region match-based filter (rMFilter) to efficiently nail down chimeric noisy long reads based on short token matches within local genomic regions. rMFilter is able to substantially accelerate long read-based SV calling pipelines without loss of effectiveness. It can be easily integrated into current long read-based pipelines to facilitate SV studies.

Availability and implementation: The C ++ source code of rMFilter is available at https://github.com/hitbc/rMFilter .

Contact: [email protected].

Supplementary information: Supplementary data are available at Bioinformatics online.

MeSH terms

  • Genome, Human
  • Genomic Structural Variation*
  • Genomics / methods*
  • Humans
  • Sequence Analysis, DNA / methods*
  • Software*