MetaSV: an accurate and integrative structural-variant caller for next generation sequencing.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 25861968.
- Also identified by DOI 10.1093/bioinformatics/btv204 and PMC identifier 4528635.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Structural variations (SVs) are large genomic rearrangements that vary significantly in size, making them challenging to detect with the relatively short reads from next-generation sequencing (NGS). Different SV detection methods have been developed; however, each is limited to specific kinds of SVs with varying accuracy and resolution. Previous works have attempted to combine different methods, but they still suffer from poor accuracy particularly for insertions. We propose MetaSV, an integrated SV caller which leverages multiple orthogonal SV signals for high accuracy and resolution. MetaSV proceeds by merging SVs from multiple tools for all types of SVs. It also analyzes soft-clipped reads from alignment to detect insertions accurately since existing tools underestimate insertion SVs. Local assembly in combination with dynamic programming is used to improve breakpoint resolution. Paired-end and coverage information is used to predict SV genotypes. Using simulation and experimental data, we demonstrate the effectiveness of MetaSV across various SV types and sizes. Code in Python is at http://bioinform.github.io/metasv/. rd@bina.com Supplementary data are available at Bioinformatics online.
Medical subject headings
- Genetic Variation
- High-Throughput Nucleotide Sequencing
- Software