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Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks

BACKGROUND: Genome-wide Association Studies (GWAS) aims to uncover the link between genomic variation and phenotype. They have been actively applied in cancer biology to investigate associations between variations and cancer phenotypes, such as susceptibility to certain types of cancer and predispos...

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Autores principales: Kim, Minsu, Huffman, Jennifer E., Justice, Amy, Goethert, Ian, Agasthya, Greeshma, Danciu, Ioana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258200/
https://www.ncbi.nlm.nih.gov/pubmed/35794577
http://dx.doi.org/10.1186/s12920-022-01298-6
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author Kim, Minsu
Huffman, Jennifer E.
Justice, Amy
Goethert, Ian
Agasthya, Greeshma
Danciu, Ioana
author_facet Kim, Minsu
Huffman, Jennifer E.
Justice, Amy
Goethert, Ian
Agasthya, Greeshma
Danciu, Ioana
author_sort Kim, Minsu
collection PubMed
description BACKGROUND: Genome-wide Association Studies (GWAS) aims to uncover the link between genomic variation and phenotype. They have been actively applied in cancer biology to investigate associations between variations and cancer phenotypes, such as susceptibility to certain types of cancer and predisposed responsiveness to specific treatments. Since GWAS primarily focuses on finding associations between individual genomic variations and cancer phenotypes, there are limitations in understanding the mechanisms by which cancer phenotypes are cooperatively affected by more than one genomic variation. RESULTS: This paper proposes a network representation learning approach to learn associations among genomic variations using a prostate cancer cohort. The learned associations are encoded into representations that can be used to identify functional modules of genomic variations within genes associated with early- and late-onset prostate cancer. The proposed method was applied to a prostate cancer cohort provided by the Veterans Administration’s Million Veteran Program to identify candidates for functional modules associated with early-onset prostate cancer. The cohort included 33,159 prostate cancer patients, 3181 early-onset patients, and 29,978 late-onset patients. The reproducibility of the proposed approach clearly showed that the proposed approach can improve the model performance in terms of robustness. CONCLUSIONS: To our knowledge, this is the first attempt to use a network representation learning approach to learn associations among genomic variations within genes. Associations learned in this way can lead to an understanding of the underlying mechanisms of how genomic variations cooperatively affect each cancer phenotype. This method can reveal unknown knowledge in the field of cancer biology and can be utilized to design more advanced cancer-targeted therapies.
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spelling pubmed-92582002022-07-07 Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks Kim, Minsu Huffman, Jennifer E. Justice, Amy Goethert, Ian Agasthya, Greeshma Danciu, Ioana BMC Med Genomics Research BACKGROUND: Genome-wide Association Studies (GWAS) aims to uncover the link between genomic variation and phenotype. They have been actively applied in cancer biology to investigate associations between variations and cancer phenotypes, such as susceptibility to certain types of cancer and predisposed responsiveness to specific treatments. Since GWAS primarily focuses on finding associations between individual genomic variations and cancer phenotypes, there are limitations in understanding the mechanisms by which cancer phenotypes are cooperatively affected by more than one genomic variation. RESULTS: This paper proposes a network representation learning approach to learn associations among genomic variations using a prostate cancer cohort. The learned associations are encoded into representations that can be used to identify functional modules of genomic variations within genes associated with early- and late-onset prostate cancer. The proposed method was applied to a prostate cancer cohort provided by the Veterans Administration’s Million Veteran Program to identify candidates for functional modules associated with early-onset prostate cancer. The cohort included 33,159 prostate cancer patients, 3181 early-onset patients, and 29,978 late-onset patients. The reproducibility of the proposed approach clearly showed that the proposed approach can improve the model performance in terms of robustness. CONCLUSIONS: To our knowledge, this is the first attempt to use a network representation learning approach to learn associations among genomic variations within genes. Associations learned in this way can lead to an understanding of the underlying mechanisms of how genomic variations cooperatively affect each cancer phenotype. This method can reveal unknown knowledge in the field of cancer biology and can be utilized to design more advanced cancer-targeted therapies. BioMed Central 2022-07-06 /pmc/articles/PMC9258200/ /pubmed/35794577 http://dx.doi.org/10.1186/s12920-022-01298-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Kim, Minsu
Huffman, Jennifer E.
Justice, Amy
Goethert, Ian
Agasthya, Greeshma
Danciu, Ioana
Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks
title Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks
title_full Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks
title_fullStr Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks
title_full_unstemmed Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks
title_short Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks
title_sort identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258200/
https://www.ncbi.nlm.nih.gov/pubmed/35794577
http://dx.doi.org/10.1186/s12920-022-01298-6
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