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Incorporating interaction networks into the determination of functionally related hit genes in genomic experiments with Markov random fields

MOTIVATION: Incorporating gene interaction data into the identification of ‘hit’ genes in genomic experiments is a well-established approach leveraging the ‘guilt by association’ assumption to obtain a network based hit list of functionally related genes. We aim to develop a method to allow for mult...

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Autores principales: Robinson, Sean, Nevalainen, Jaakko, Pinna, Guillaume, Campalans, Anna, Radicella, J Pablo, Guyon, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870666/
https://www.ncbi.nlm.nih.gov/pubmed/28881978
http://dx.doi.org/10.1093/bioinformatics/btx244
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author Robinson, Sean
Nevalainen, Jaakko
Pinna, Guillaume
Campalans, Anna
Radicella, J Pablo
Guyon, Laurent
author_facet Robinson, Sean
Nevalainen, Jaakko
Pinna, Guillaume
Campalans, Anna
Radicella, J Pablo
Guyon, Laurent
author_sort Robinson, Sean
collection PubMed
description MOTIVATION: Incorporating gene interaction data into the identification of ‘hit’ genes in genomic experiments is a well-established approach leveraging the ‘guilt by association’ assumption to obtain a network based hit list of functionally related genes. We aim to develop a method to allow for multivariate gene scores and multiple hit labels in order to extend the analysis of genomic screening data within such an approach. RESULTS: We propose a Markov random field-based method to achieve our aim and show that the particular advantages of our method compared with those currently used lead to new insights in previously analysed data as well as for our own motivating data. Our method additionally achieves the best performance in an independent simulation experiment. The real data applications we consider comprise of a survival analysis and differential expression experiment and a cell-based RNA interference functional screen. AVAILABILITY AND IMPLEMENTATION: We provide all of the data and code related to the results in the paper. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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spelling pubmed-58706662018-04-05 Incorporating interaction networks into the determination of functionally related hit genes in genomic experiments with Markov random fields Robinson, Sean Nevalainen, Jaakko Pinna, Guillaume Campalans, Anna Radicella, J Pablo Guyon, Laurent Bioinformatics Ismb/Eccb 2017: The 25th Annual Conference Intelligent Systems for Molecular Biology Held Jointly with the 16th Annual European Conference on Computational Biology, Prague, Czech Republic, July 21–25, 2017 MOTIVATION: Incorporating gene interaction data into the identification of ‘hit’ genes in genomic experiments is a well-established approach leveraging the ‘guilt by association’ assumption to obtain a network based hit list of functionally related genes. We aim to develop a method to allow for multivariate gene scores and multiple hit labels in order to extend the analysis of genomic screening data within such an approach. RESULTS: We propose a Markov random field-based method to achieve our aim and show that the particular advantages of our method compared with those currently used lead to new insights in previously analysed data as well as for our own motivating data. Our method additionally achieves the best performance in an independent simulation experiment. The real data applications we consider comprise of a survival analysis and differential expression experiment and a cell-based RNA interference functional screen. AVAILABILITY AND IMPLEMENTATION: We provide all of the data and code related to the results in the paper. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2017-07-15 2017-07-12 /pmc/articles/PMC5870666/ /pubmed/28881978 http://dx.doi.org/10.1093/bioinformatics/btx244 Text en © The Author 2017. 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 Ismb/Eccb 2017: The 25th Annual Conference Intelligent Systems for Molecular Biology Held Jointly with the 16th Annual European Conference on Computational Biology, Prague, Czech Republic, July 21–25, 2017
Robinson, Sean
Nevalainen, Jaakko
Pinna, Guillaume
Campalans, Anna
Radicella, J Pablo
Guyon, Laurent
Incorporating interaction networks into the determination of functionally related hit genes in genomic experiments with Markov random fields
title Incorporating interaction networks into the determination of functionally related hit genes in genomic experiments with Markov random fields
title_full Incorporating interaction networks into the determination of functionally related hit genes in genomic experiments with Markov random fields
title_fullStr Incorporating interaction networks into the determination of functionally related hit genes in genomic experiments with Markov random fields
title_full_unstemmed Incorporating interaction networks into the determination of functionally related hit genes in genomic experiments with Markov random fields
title_short Incorporating interaction networks into the determination of functionally related hit genes in genomic experiments with Markov random fields
title_sort incorporating interaction networks into the determination of functionally related hit genes in genomic experiments with markov random fields
topic Ismb/Eccb 2017: The 25th Annual Conference Intelligent Systems for Molecular Biology Held Jointly with the 16th Annual European Conference on Computational Biology, Prague, Czech Republic, July 21–25, 2017
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870666/
https://www.ncbi.nlm.nih.gov/pubmed/28881978
http://dx.doi.org/10.1093/bioinformatics/btx244
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