GenomeWarp: an alignment-based variant coordinate transformation.
basic_science · Level V
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- Record sourced from PubMed, PMID 30916319.
- Also identified by DOI 10.1093/bioinformatics/btz218 and PMC identifier 6821237.
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Abstract
Reference genomes are refined to reflect error corrections and other improvements. While this process improves novel data generation and analysis, incorporating data analyzed on an older reference genome assembly requires transforming the coordinates and representations of the data to the new assembly. Multiple tools exist to perform this transformation for coordinate-only data types, but none supports accurate transformation of genome-wide short variation. Here we present GenomeWarp, a tool for efficiently transforming variants between genome assemblies. GenomeWarp transforms regions and short variants in a conservative manner to minimize false positive and negative variants in the target genome, and converts over 99% of regions and short variants from a representative human genome. GenomeWarp is written in Java. All source code and the user manual are freely available at https://github.com/verilylifesciences/genomewarp. Supplementary data are available at Bioinformatics online.
Medical subject headings
- Genomics
- Software