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A strategy for extracting and analyzing large-scale quantitative epistatic interaction data

Recently, approaches have been developed for high-throughput identification of synthetic sick/lethal gene pairs. However, these are only a specific example of the broader phenomenon of epistasis, wherein the presence of one mutation modulates the phenotype of another. We present analysis techniques...

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Detalles Bibliográficos
Autores principales: Collins, Sean R, Schuldiner, Maya, Krogan, Nevan J, Weissman, Jonathan S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1779568/
https://www.ncbi.nlm.nih.gov/pubmed/16859555
http://dx.doi.org/10.1186/gb-2006-7-7-r63
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author Collins, Sean R
Schuldiner, Maya
Krogan, Nevan J
Weissman, Jonathan S
author_facet Collins, Sean R
Schuldiner, Maya
Krogan, Nevan J
Weissman, Jonathan S
author_sort Collins, Sean R
collection PubMed
description Recently, approaches have been developed for high-throughput identification of synthetic sick/lethal gene pairs. However, these are only a specific example of the broader phenomenon of epistasis, wherein the presence of one mutation modulates the phenotype of another. We present analysis techniques for generating high-confidence quantitative epistasis scores from measurements made using synthetic genetic array and epistatic miniarray profile (E-MAP) technology, as well as several tools for higher-level analysis of the resulting data that are greatly enhanced by the quantitative score and detection of alleviating interactions.
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spelling pubmed-17795682007-01-19 A strategy for extracting and analyzing large-scale quantitative epistatic interaction data Collins, Sean R Schuldiner, Maya Krogan, Nevan J Weissman, Jonathan S Genome Biol Method Recently, approaches have been developed for high-throughput identification of synthetic sick/lethal gene pairs. However, these are only a specific example of the broader phenomenon of epistasis, wherein the presence of one mutation modulates the phenotype of another. We present analysis techniques for generating high-confidence quantitative epistasis scores from measurements made using synthetic genetic array and epistatic miniarray profile (E-MAP) technology, as well as several tools for higher-level analysis of the resulting data that are greatly enhanced by the quantitative score and detection of alleviating interactions. BioMed Central 2006 2006-07-21 /pmc/articles/PMC1779568/ /pubmed/16859555 http://dx.doi.org/10.1186/gb-2006-7-7-r63 Text en Copyright © 2006 Collins et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Method
Collins, Sean R
Schuldiner, Maya
Krogan, Nevan J
Weissman, Jonathan S
A strategy for extracting and analyzing large-scale quantitative epistatic interaction data
title A strategy for extracting and analyzing large-scale quantitative epistatic interaction data
title_full A strategy for extracting and analyzing large-scale quantitative epistatic interaction data
title_fullStr A strategy for extracting and analyzing large-scale quantitative epistatic interaction data
title_full_unstemmed A strategy for extracting and analyzing large-scale quantitative epistatic interaction data
title_short A strategy for extracting and analyzing large-scale quantitative epistatic interaction data
title_sort strategy for extracting and analyzing large-scale quantitative epistatic interaction data
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1779568/
https://www.ncbi.nlm.nih.gov/pubmed/16859555
http://dx.doi.org/10.1186/gb-2006-7-7-r63
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