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Pheno2Geno - High-throughput generation of genetic markers and maps from molecular phenotypes for crosses between inbred strains
BACKGROUND: Genetic markers and maps are instrumental in quantitative trait locus (QTL) mapping in segregating populations. The resolution of QTL localization depends on the number of informative recombinations in the population and how well they are tagged by markers. Larger populations and denser...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339742/ https://www.ncbi.nlm.nih.gov/pubmed/25886992 http://dx.doi.org/10.1186/s12859-015-0475-6 |
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author | Zych, Konrad Li, Yang van der Velde, Joeri K Joosen, Ronny VL Ligterink, Wilco Jansen, Ritsert C Arends, Danny |
author_facet | Zych, Konrad Li, Yang van der Velde, Joeri K Joosen, Ronny VL Ligterink, Wilco Jansen, Ritsert C Arends, Danny |
author_sort | Zych, Konrad |
collection | PubMed |
description | BACKGROUND: Genetic markers and maps are instrumental in quantitative trait locus (QTL) mapping in segregating populations. The resolution of QTL localization depends on the number of informative recombinations in the population and how well they are tagged by markers. Larger populations and denser marker maps are better for detecting and locating QTLs. Marker maps that are initially too sparse can be saturated or derived de novo from high-throughput omics data, (e.g. gene expression, protein or metabolite abundance). If these molecular phenotypes are affected by genetic variation due to a major QTL they will show a clear multimodal distribution. Using this information, phenotypes can be converted into genetic markers. RESULTS: The Pheno2Geno tool uses mixture modeling to select phenotypes and transform them into genetic markers suitable for construction and/or saturation of a genetic map. Pheno2Geno excludes candidate genetic markers that show evidence for multiple possibly epistatically interacting QTL and/or interaction with the environment, in order to provide a set of robust markers for follow-up QTL mapping. We demonstrate the use of Pheno2Geno on gene expression data of 370,000 probes in 148 A. thaliana recombinant inbred lines. Pheno2Geno is able to saturate the existing genetic map, decreasing the average distance between markers from 7.1 cM to 0.89 cM, close to the theoretical limit of 0.68 cM (with 148 individuals we expect a recombination every 100/148=0.68 cM); this pinpointed almost all of the informative recombinations in the population. CONCLUSION: The Pheno2Geno package makes use of genome-wide molecular profiling and provides a tool for high-throughput de novo map construction and saturation of existing genetic maps. Processing of the showcase dataset takes less than 30 minutes on an average desktop PC. Pheno2Geno improves QTL mapping results at no additional laboratory cost and with minimum computational effort. Its results are formatted for direct use in R/qtl, the leading R package for QTL studies. Pheno2Geno is freely available on CRAN under “GNU GPL v3”. The Pheno2Geno package as well as the tutorial can also be found at: http://pheno2geno.nl. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-015-0475-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4339742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43397422015-02-26 Pheno2Geno - High-throughput generation of genetic markers and maps from molecular phenotypes for crosses between inbred strains Zych, Konrad Li, Yang van der Velde, Joeri K Joosen, Ronny VL Ligterink, Wilco Jansen, Ritsert C Arends, Danny BMC Bioinformatics Software BACKGROUND: Genetic markers and maps are instrumental in quantitative trait locus (QTL) mapping in segregating populations. The resolution of QTL localization depends on the number of informative recombinations in the population and how well they are tagged by markers. Larger populations and denser marker maps are better for detecting and locating QTLs. Marker maps that are initially too sparse can be saturated or derived de novo from high-throughput omics data, (e.g. gene expression, protein or metabolite abundance). If these molecular phenotypes are affected by genetic variation due to a major QTL they will show a clear multimodal distribution. Using this information, phenotypes can be converted into genetic markers. RESULTS: The Pheno2Geno tool uses mixture modeling to select phenotypes and transform them into genetic markers suitable for construction and/or saturation of a genetic map. Pheno2Geno excludes candidate genetic markers that show evidence for multiple possibly epistatically interacting QTL and/or interaction with the environment, in order to provide a set of robust markers for follow-up QTL mapping. We demonstrate the use of Pheno2Geno on gene expression data of 370,000 probes in 148 A. thaliana recombinant inbred lines. Pheno2Geno is able to saturate the existing genetic map, decreasing the average distance between markers from 7.1 cM to 0.89 cM, close to the theoretical limit of 0.68 cM (with 148 individuals we expect a recombination every 100/148=0.68 cM); this pinpointed almost all of the informative recombinations in the population. CONCLUSION: The Pheno2Geno package makes use of genome-wide molecular profiling and provides a tool for high-throughput de novo map construction and saturation of existing genetic maps. Processing of the showcase dataset takes less than 30 minutes on an average desktop PC. Pheno2Geno improves QTL mapping results at no additional laboratory cost and with minimum computational effort. Its results are formatted for direct use in R/qtl, the leading R package for QTL studies. Pheno2Geno is freely available on CRAN under “GNU GPL v3”. The Pheno2Geno package as well as the tutorial can also be found at: http://pheno2geno.nl. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-015-0475-6) contains supplementary material, which is available to authorized users. BioMed Central 2015-02-19 /pmc/articles/PMC4339742/ /pubmed/25886992 http://dx.doi.org/10.1186/s12859-015-0475-6 Text en © Zych et al.; licensee BioMed Central. 2015 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 use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Software Zych, Konrad Li, Yang van der Velde, Joeri K Joosen, Ronny VL Ligterink, Wilco Jansen, Ritsert C Arends, Danny Pheno2Geno - High-throughput generation of genetic markers and maps from molecular phenotypes for crosses between inbred strains |
title | Pheno2Geno - High-throughput generation of genetic markers and maps from molecular phenotypes for crosses between inbred strains |
title_full | Pheno2Geno - High-throughput generation of genetic markers and maps from molecular phenotypes for crosses between inbred strains |
title_fullStr | Pheno2Geno - High-throughput generation of genetic markers and maps from molecular phenotypes for crosses between inbred strains |
title_full_unstemmed | Pheno2Geno - High-throughput generation of genetic markers and maps from molecular phenotypes for crosses between inbred strains |
title_short | Pheno2Geno - High-throughput generation of genetic markers and maps from molecular phenotypes for crosses between inbred strains |
title_sort | pheno2geno - high-throughput generation of genetic markers and maps from molecular phenotypes for crosses between inbred strains |
topic | Software |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4339742/ https://www.ncbi.nlm.nih.gov/pubmed/25886992 http://dx.doi.org/10.1186/s12859-015-0475-6 |
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