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GenomeWarp: an alignment-based variant coordinate transformation
SUMMARY: 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 n...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821237/ https://www.ncbi.nlm.nih.gov/pubmed/30916319 http://dx.doi.org/10.1093/bioinformatics/btz218 |
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author | McLean, Cory Y Hwang, Yeongwoo Poplin, Ryan DePristo, Mark A |
author_facet | McLean, Cory Y Hwang, Yeongwoo Poplin, Ryan DePristo, Mark A |
author_sort | McLean, Cory Y |
collection | PubMed |
description | SUMMARY: 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. AVAILABILITY AND IMPLEMENTATION: GenomeWarp is written in Java. All source code and the user manual are freely available at https://github.com/verilylifesciences/genomewarp. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-6821237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-68212372019-11-04 GenomeWarp: an alignment-based variant coordinate transformation McLean, Cory Y Hwang, Yeongwoo Poplin, Ryan DePristo, Mark A Bioinformatics Applications Notes SUMMARY: 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. AVAILABILITY AND IMPLEMENTATION: GenomeWarp is written in Java. All source code and the user manual are freely available at https://github.com/verilylifesciences/genomewarp. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2019-11-01 2019-03-27 /pmc/articles/PMC6821237/ /pubmed/30916319 http://dx.doi.org/10.1093/bioinformatics/btz218 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Applications Notes McLean, Cory Y Hwang, Yeongwoo Poplin, Ryan DePristo, Mark A GenomeWarp: an alignment-based variant coordinate transformation |
title | GenomeWarp: an alignment-based variant coordinate transformation |
title_full | GenomeWarp: an alignment-based variant coordinate transformation |
title_fullStr | GenomeWarp: an alignment-based variant coordinate transformation |
title_full_unstemmed | GenomeWarp: an alignment-based variant coordinate transformation |
title_short | GenomeWarp: an alignment-based variant coordinate transformation |
title_sort | genomewarp: an alignment-based variant coordinate transformation |
topic | Applications Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6821237/ https://www.ncbi.nlm.nih.gov/pubmed/30916319 http://dx.doi.org/10.1093/bioinformatics/btz218 |
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