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ExpansionHunter: a sequence-graph-based tool to analyze variation in short tandem repeat regions

SUMMARY: We describe a novel computational method for genotyping repeats using sequence graphs. This method addresses the long-standing need to accurately genotype medically important loci containing repeats adjacent to other variants or imperfect DNA repeats such as polyalanine repeats. Here we int...

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Autores principales: Dolzhenko, Egor, Deshpande, Viraj, Schlesinger, Felix, Krusche, Peter, Petrovski, Roman, Chen, Sai, Emig-Agius, Dorothea, Gross, Andrew, Narzisi, Giuseppe, Bowman, Brett, Scheffler, Konrad, van Vugt, Joke J F A, French, Courtney, Sanchis-Juan, Alba, Ibáñez, Kristina, Tucci, Arianna, Lajoie, Bryan R, Veldink, Jan H, Raymond, F Lucy, Taft, Ryan J, Bentley, David R, Eberle, Michael A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853681/
https://www.ncbi.nlm.nih.gov/pubmed/31134279
http://dx.doi.org/10.1093/bioinformatics/btz431
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author Dolzhenko, Egor
Deshpande, Viraj
Schlesinger, Felix
Krusche, Peter
Petrovski, Roman
Chen, Sai
Emig-Agius, Dorothea
Gross, Andrew
Narzisi, Giuseppe
Bowman, Brett
Scheffler, Konrad
van Vugt, Joke J F A
French, Courtney
Sanchis-Juan, Alba
Ibáñez, Kristina
Tucci, Arianna
Lajoie, Bryan R
Veldink, Jan H
Raymond, F Lucy
Taft, Ryan J
Bentley, David R
Eberle, Michael A
author_facet Dolzhenko, Egor
Deshpande, Viraj
Schlesinger, Felix
Krusche, Peter
Petrovski, Roman
Chen, Sai
Emig-Agius, Dorothea
Gross, Andrew
Narzisi, Giuseppe
Bowman, Brett
Scheffler, Konrad
van Vugt, Joke J F A
French, Courtney
Sanchis-Juan, Alba
Ibáñez, Kristina
Tucci, Arianna
Lajoie, Bryan R
Veldink, Jan H
Raymond, F Lucy
Taft, Ryan J
Bentley, David R
Eberle, Michael A
author_sort Dolzhenko, Egor
collection PubMed
description SUMMARY: We describe a novel computational method for genotyping repeats using sequence graphs. This method addresses the long-standing need to accurately genotype medically important loci containing repeats adjacent to other variants or imperfect DNA repeats such as polyalanine repeats. Here we introduce a new version of our repeat genotyping software, ExpansionHunter, that uses this method to perform targeted genotyping of a broad class of such loci. AVAILABILITY AND IMPLEMENTATION: ExpansionHunter is implemented in C++ and is available under the Apache License Version 2.0. The source code, documentation, and Linux/macOS binaries are available at https://github.com/Illumina/ExpansionHunter/. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-68536812019-11-19 ExpansionHunter: a sequence-graph-based tool to analyze variation in short tandem repeat regions Dolzhenko, Egor Deshpande, Viraj Schlesinger, Felix Krusche, Peter Petrovski, Roman Chen, Sai Emig-Agius, Dorothea Gross, Andrew Narzisi, Giuseppe Bowman, Brett Scheffler, Konrad van Vugt, Joke J F A French, Courtney Sanchis-Juan, Alba Ibáñez, Kristina Tucci, Arianna Lajoie, Bryan R Veldink, Jan H Raymond, F Lucy Taft, Ryan J Bentley, David R Eberle, Michael A Bioinformatics Applications Notes SUMMARY: We describe a novel computational method for genotyping repeats using sequence graphs. This method addresses the long-standing need to accurately genotype medically important loci containing repeats adjacent to other variants or imperfect DNA repeats such as polyalanine repeats. Here we introduce a new version of our repeat genotyping software, ExpansionHunter, that uses this method to perform targeted genotyping of a broad class of such loci. AVAILABILITY AND IMPLEMENTATION: ExpansionHunter is implemented in C++ and is available under the Apache License Version 2.0. The source code, documentation, and Linux/macOS binaries are available at https://github.com/Illumina/ExpansionHunter/. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2019-11-15 2019-05-27 /pmc/articles/PMC6853681/ /pubmed/31134279 http://dx.doi.org/10.1093/bioinformatics/btz431 Text en © The Author(s) 2019. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Applications Notes
Dolzhenko, Egor
Deshpande, Viraj
Schlesinger, Felix
Krusche, Peter
Petrovski, Roman
Chen, Sai
Emig-Agius, Dorothea
Gross, Andrew
Narzisi, Giuseppe
Bowman, Brett
Scheffler, Konrad
van Vugt, Joke J F A
French, Courtney
Sanchis-Juan, Alba
Ibáñez, Kristina
Tucci, Arianna
Lajoie, Bryan R
Veldink, Jan H
Raymond, F Lucy
Taft, Ryan J
Bentley, David R
Eberle, Michael A
ExpansionHunter: a sequence-graph-based tool to analyze variation in short tandem repeat regions
title ExpansionHunter: a sequence-graph-based tool to analyze variation in short tandem repeat regions
title_full ExpansionHunter: a sequence-graph-based tool to analyze variation in short tandem repeat regions
title_fullStr ExpansionHunter: a sequence-graph-based tool to analyze variation in short tandem repeat regions
title_full_unstemmed ExpansionHunter: a sequence-graph-based tool to analyze variation in short tandem repeat regions
title_short ExpansionHunter: a sequence-graph-based tool to analyze variation in short tandem repeat regions
title_sort expansionhunter: a sequence-graph-based tool to analyze variation in short tandem repeat regions
topic Applications Notes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6853681/
https://www.ncbi.nlm.nih.gov/pubmed/31134279
http://dx.doi.org/10.1093/bioinformatics/btz431
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