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Mapping Challenging Mutations by Whole-Genome Sequencing
Whole-genome sequencing provides a rapid and powerful method for identifying mutations on a global scale, and has spurred a renewed enthusiasm for classical genetic screens in model organisms. The most commonly characterized category of mutation consists of monogenic, recessive traits, due to their...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Genetics Society of America
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4856081/ https://www.ncbi.nlm.nih.gov/pubmed/26945029 http://dx.doi.org/10.1534/g3.116.028316 |
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author | Smith, Harold E. Fabritius, Amy S. Jaramillo-Lambert, Aimee Golden, Andy |
author_facet | Smith, Harold E. Fabritius, Amy S. Jaramillo-Lambert, Aimee Golden, Andy |
author_sort | Smith, Harold E. |
collection | PubMed |
description | Whole-genome sequencing provides a rapid and powerful method for identifying mutations on a global scale, and has spurred a renewed enthusiasm for classical genetic screens in model organisms. The most commonly characterized category of mutation consists of monogenic, recessive traits, due to their genetic tractability. Therefore, most of the mapping methods for mutation identification by whole-genome sequencing are directed toward alleles that fulfill those criteria (i.e., single-gene, homozygous variants). However, such approaches are not entirely suitable for the characterization of a variety of more challenging mutations, such as dominant and semidominant alleles or multigenic traits. Therefore, we have developed strategies for the identification of those classes of mutations, using polymorphism mapping in Caenorhabditis elegans as our model for validation. We also report an alternative approach for mutation identification from traditional recombinant crosses, and a solution to the technical challenge of sequencing sterile or terminally arrested strains where population size is limiting. The methods described herein extend the applicability of whole-genome sequencing to a broader spectrum of mutations, including classes that are difficult to map by traditional means. |
format | Online Article Text |
id | pubmed-4856081 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Genetics Society of America |
record_format | MEDLINE/PubMed |
spelling | pubmed-48560812016-05-05 Mapping Challenging Mutations by Whole-Genome Sequencing Smith, Harold E. Fabritius, Amy S. Jaramillo-Lambert, Aimee Golden, Andy G3 (Bethesda) Investigations Whole-genome sequencing provides a rapid and powerful method for identifying mutations on a global scale, and has spurred a renewed enthusiasm for classical genetic screens in model organisms. The most commonly characterized category of mutation consists of monogenic, recessive traits, due to their genetic tractability. Therefore, most of the mapping methods for mutation identification by whole-genome sequencing are directed toward alleles that fulfill those criteria (i.e., single-gene, homozygous variants). However, such approaches are not entirely suitable for the characterization of a variety of more challenging mutations, such as dominant and semidominant alleles or multigenic traits. Therefore, we have developed strategies for the identification of those classes of mutations, using polymorphism mapping in Caenorhabditis elegans as our model for validation. We also report an alternative approach for mutation identification from traditional recombinant crosses, and a solution to the technical challenge of sequencing sterile or terminally arrested strains where population size is limiting. The methods described herein extend the applicability of whole-genome sequencing to a broader spectrum of mutations, including classes that are difficult to map by traditional means. Genetics Society of America 2016-03-04 /pmc/articles/PMC4856081/ /pubmed/26945029 http://dx.doi.org/10.1534/g3.116.028316 Text en Copyright © 2016 Smith et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Investigations Smith, Harold E. Fabritius, Amy S. Jaramillo-Lambert, Aimee Golden, Andy Mapping Challenging Mutations by Whole-Genome Sequencing |
title | Mapping Challenging Mutations by Whole-Genome Sequencing |
title_full | Mapping Challenging Mutations by Whole-Genome Sequencing |
title_fullStr | Mapping Challenging Mutations by Whole-Genome Sequencing |
title_full_unstemmed | Mapping Challenging Mutations by Whole-Genome Sequencing |
title_short | Mapping Challenging Mutations by Whole-Genome Sequencing |
title_sort | mapping challenging mutations by whole-genome sequencing |
topic | Investigations |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4856081/ https://www.ncbi.nlm.nih.gov/pubmed/26945029 http://dx.doi.org/10.1534/g3.116.028316 |
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