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SVIM-asm: structural variant detection from haploid and diploid genome assemblies
MOTIVATION: With the availability of new sequencing technologies, the generation of haplotype-resolved genome assemblies up to chromosome scale has become feasible. These assemblies capture the complete genetic information of both parental haplotypes, increase structural variant (SV) calling sensiti...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016491/ https://www.ncbi.nlm.nih.gov/pubmed/33346817 http://dx.doi.org/10.1093/bioinformatics/btaa1034 |
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author | Heller, David Vingron, Martin |
author_facet | Heller, David Vingron, Martin |
author_sort | Heller, David |
collection | PubMed |
description | MOTIVATION: With the availability of new sequencing technologies, the generation of haplotype-resolved genome assemblies up to chromosome scale has become feasible. These assemblies capture the complete genetic information of both parental haplotypes, increase structural variant (SV) calling sensitivity and enable direct genotyping and phasing of SVs. Yet, existing SV callers are designed for haploid genome assemblies only, do not support genotyping or detect only a limited set of SV classes. RESULTS: We introduce our method SVIM-asm for the detection and genotyping of six common classes of SVs from haploid and diploid genome assemblies. Compared against the only other existing SV caller for diploid assemblies, DipCall, SVIM-asm detects more SV classes and reached higher F1 scores for the detection of insertions and deletions on two recently published assemblies of the HG002 individual. AVAILABILITY AND IMPLEMENTATION: SVIM-asm has been implemented in Python and can be easily installed via bioconda. Its source code is available at github.com/eldariont/svim-asm. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-8016491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-80164912021-04-07 SVIM-asm: structural variant detection from haploid and diploid genome assemblies Heller, David Vingron, Martin Bioinformatics Applications Notes MOTIVATION: With the availability of new sequencing technologies, the generation of haplotype-resolved genome assemblies up to chromosome scale has become feasible. These assemblies capture the complete genetic information of both parental haplotypes, increase structural variant (SV) calling sensitivity and enable direct genotyping and phasing of SVs. Yet, existing SV callers are designed for haploid genome assemblies only, do not support genotyping or detect only a limited set of SV classes. RESULTS: We introduce our method SVIM-asm for the detection and genotyping of six common classes of SVs from haploid and diploid genome assemblies. Compared against the only other existing SV caller for diploid assemblies, DipCall, SVIM-asm detects more SV classes and reached higher F1 scores for the detection of insertions and deletions on two recently published assemblies of the HG002 individual. AVAILABILITY AND IMPLEMENTATION: SVIM-asm has been implemented in Python and can be easily installed via bioconda. Its source code is available at github.com/eldariont/svim-asm. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2020-12-21 /pmc/articles/PMC8016491/ /pubmed/33346817 http://dx.doi.org/10.1093/bioinformatics/btaa1034 Text en © The Author(s) 2020. 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 Heller, David Vingron, Martin SVIM-asm: structural variant detection from haploid and diploid genome assemblies |
title | SVIM-asm: structural variant detection from haploid and diploid genome assemblies |
title_full | SVIM-asm: structural variant detection from haploid and diploid genome assemblies |
title_fullStr | SVIM-asm: structural variant detection from haploid and diploid genome assemblies |
title_full_unstemmed | SVIM-asm: structural variant detection from haploid and diploid genome assemblies |
title_short | SVIM-asm: structural variant detection from haploid and diploid genome assemblies |
title_sort | svim-asm: structural variant detection from haploid and diploid genome assemblies |
topic | Applications Notes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016491/ https://www.ncbi.nlm.nih.gov/pubmed/33346817 http://dx.doi.org/10.1093/bioinformatics/btaa1034 |
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