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HomozygosityMapper2012—bridging the gap between homozygosity mapping and deep sequencing

Homozygosity mapping is a common method to map recessive traits in consanguineous families. To facilitate these analyses, we have developed HomozygosityMapper, a web-based approach to homozygosity mapping. HomozygosityMapper allows researchers to directly upload the genotype files produced by the ma...

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Detalles Bibliográficos
Autores principales: Seelow, Dominik, Schuelke, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394249/
https://www.ncbi.nlm.nih.gov/pubmed/22669902
http://dx.doi.org/10.1093/nar/gks487
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author Seelow, Dominik
Schuelke, Markus
author_facet Seelow, Dominik
Schuelke, Markus
author_sort Seelow, Dominik
collection PubMed
description Homozygosity mapping is a common method to map recessive traits in consanguineous families. To facilitate these analyses, we have developed HomozygosityMapper, a web-based approach to homozygosity mapping. HomozygosityMapper allows researchers to directly upload the genotype files produced by the major genotyping platforms as well as deep sequencing data. It detects stretches of homozygosity shared by the affected individuals and displays them graphically. Users can interactively inspect the underlying genotypes, manually refine these regions and eventually submit them to our candidate gene search engine GeneDistiller to identify the most promising candidate genes. Here, we present the new version of HomozygosityMapper. The most striking new feature is the support of Next Generation Sequencing *.vcf files as input. Upon users’ requests, we have implemented the analysis of common experimental rodents as well as of important farm animals. Furthermore, we have extended the options for single families and loss of heterozygosity studies. Another new feature is the export of *.bed files for targeted enrichment of the potential disease regions for deep sequencing strategies. HomozygosityMapper also generates files for conventional linkage analyses which are already restricted to the possible disease regions, hence superseding CPU-intensive genome-wide analyses. HomozygosityMapper is freely available at http://www.homozygositymapper.org/.
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spelling pubmed-33942492012-07-30 HomozygosityMapper2012—bridging the gap between homozygosity mapping and deep sequencing Seelow, Dominik Schuelke, Markus Nucleic Acids Res Articles Homozygosity mapping is a common method to map recessive traits in consanguineous families. To facilitate these analyses, we have developed HomozygosityMapper, a web-based approach to homozygosity mapping. HomozygosityMapper allows researchers to directly upload the genotype files produced by the major genotyping platforms as well as deep sequencing data. It detects stretches of homozygosity shared by the affected individuals and displays them graphically. Users can interactively inspect the underlying genotypes, manually refine these regions and eventually submit them to our candidate gene search engine GeneDistiller to identify the most promising candidate genes. Here, we present the new version of HomozygosityMapper. The most striking new feature is the support of Next Generation Sequencing *.vcf files as input. Upon users’ requests, we have implemented the analysis of common experimental rodents as well as of important farm animals. Furthermore, we have extended the options for single families and loss of heterozygosity studies. Another new feature is the export of *.bed files for targeted enrichment of the potential disease regions for deep sequencing strategies. HomozygosityMapper also generates files for conventional linkage analyses which are already restricted to the possible disease regions, hence superseding CPU-intensive genome-wide analyses. HomozygosityMapper is freely available at http://www.homozygositymapper.org/. Oxford University Press 2012-07 2012-06-04 /pmc/articles/PMC3394249/ /pubmed/22669902 http://dx.doi.org/10.1093/nar/gks487 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Seelow, Dominik
Schuelke, Markus
HomozygosityMapper2012—bridging the gap between homozygosity mapping and deep sequencing
title HomozygosityMapper2012—bridging the gap between homozygosity mapping and deep sequencing
title_full HomozygosityMapper2012—bridging the gap between homozygosity mapping and deep sequencing
title_fullStr HomozygosityMapper2012—bridging the gap between homozygosity mapping and deep sequencing
title_full_unstemmed HomozygosityMapper2012—bridging the gap between homozygosity mapping and deep sequencing
title_short HomozygosityMapper2012—bridging the gap between homozygosity mapping and deep sequencing
title_sort homozygositymapper2012—bridging the gap between homozygosity mapping and deep sequencing
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3394249/
https://www.ncbi.nlm.nih.gov/pubmed/22669902
http://dx.doi.org/10.1093/nar/gks487
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