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Integrative eQTL-weighted hierarchical Cox models for SNP-set based time-to-event association studies
BACKGROUND: Integrating functional annotations into SNP-set association studies has been proven a powerful analysis strategy. Statistical methods for such integration have been developed for continuous and binary phenotypes; however, the SNP-set integrative approaches for time-to-event or survival o...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502405/ https://www.ncbi.nlm.nih.gov/pubmed/34627275 http://dx.doi.org/10.1186/s12967-021-03090-z |
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author | Lu, Haojie Wei, Yongyue Jiang, Zhou Zhang, Jinhui Wang, Ting Huang, Shuiping Zeng, Ping |
author_facet | Lu, Haojie Wei, Yongyue Jiang, Zhou Zhang, Jinhui Wang, Ting Huang, Shuiping Zeng, Ping |
author_sort | Lu, Haojie |
collection | PubMed |
description | BACKGROUND: Integrating functional annotations into SNP-set association studies has been proven a powerful analysis strategy. Statistical methods for such integration have been developed for continuous and binary phenotypes; however, the SNP-set integrative approaches for time-to-event or survival outcomes are lacking. METHODS: We here propose IEHC, an integrative eQTL (expression quantitative trait loci) hierarchical Cox regression, for SNP-set based survival association analysis by modeling effect sizes of genetic variants as a function of eQTL via a hierarchical manner. Three p-values combination tests are developed to examine the joint effects of eQTL and genetic variants after a novel decorrelated modification of statistics for the two components. An omnibus test (IEHC-ACAT) is further adapted to aggregate the strengths of all available tests. RESULTS: Simulations demonstrated that the IEHC joint tests were more powerful if both eQTL and genetic variants contributed to association signal, while IEHC-ACAT was robust and often outperformed other approaches across various simulation scenarios. When applying IEHC to ten TCGA cancers by incorporating eQTL from relevant tissues of GTEx, we revealed that substantial correlations existed between the two types of effect sizes of genetic variants from TCGA and GTEx, and identified 21 (9 unique) cancer-associated genes which would otherwise be missed by approaches not incorporating eQTL. CONCLUSION: IEHC represents a flexible, robust, and powerful approach to integrate functional omics information to enhance the power of identifying association signals for the survival risk of complex human cancers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-021-03090-z. |
format | Online Article Text |
id | pubmed-8502405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-85024052021-10-20 Integrative eQTL-weighted hierarchical Cox models for SNP-set based time-to-event association studies Lu, Haojie Wei, Yongyue Jiang, Zhou Zhang, Jinhui Wang, Ting Huang, Shuiping Zeng, Ping J Transl Med Research BACKGROUND: Integrating functional annotations into SNP-set association studies has been proven a powerful analysis strategy. Statistical methods for such integration have been developed for continuous and binary phenotypes; however, the SNP-set integrative approaches for time-to-event or survival outcomes are lacking. METHODS: We here propose IEHC, an integrative eQTL (expression quantitative trait loci) hierarchical Cox regression, for SNP-set based survival association analysis by modeling effect sizes of genetic variants as a function of eQTL via a hierarchical manner. Three p-values combination tests are developed to examine the joint effects of eQTL and genetic variants after a novel decorrelated modification of statistics for the two components. An omnibus test (IEHC-ACAT) is further adapted to aggregate the strengths of all available tests. RESULTS: Simulations demonstrated that the IEHC joint tests were more powerful if both eQTL and genetic variants contributed to association signal, while IEHC-ACAT was robust and often outperformed other approaches across various simulation scenarios. When applying IEHC to ten TCGA cancers by incorporating eQTL from relevant tissues of GTEx, we revealed that substantial correlations existed between the two types of effect sizes of genetic variants from TCGA and GTEx, and identified 21 (9 unique) cancer-associated genes which would otherwise be missed by approaches not incorporating eQTL. CONCLUSION: IEHC represents a flexible, robust, and powerful approach to integrate functional omics information to enhance the power of identifying association signals for the survival risk of complex human cancers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12967-021-03090-z. BioMed Central 2021-10-09 /pmc/articles/PMC8502405/ /pubmed/34627275 http://dx.doi.org/10.1186/s12967-021-03090-z Text en © The Author(s) 2021 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 Lu, Haojie Wei, Yongyue Jiang, Zhou Zhang, Jinhui Wang, Ting Huang, Shuiping Zeng, Ping Integrative eQTL-weighted hierarchical Cox models for SNP-set based time-to-event association studies |
title | Integrative eQTL-weighted hierarchical Cox models for SNP-set based time-to-event association studies |
title_full | Integrative eQTL-weighted hierarchical Cox models for SNP-set based time-to-event association studies |
title_fullStr | Integrative eQTL-weighted hierarchical Cox models for SNP-set based time-to-event association studies |
title_full_unstemmed | Integrative eQTL-weighted hierarchical Cox models for SNP-set based time-to-event association studies |
title_short | Integrative eQTL-weighted hierarchical Cox models for SNP-set based time-to-event association studies |
title_sort | integrative eqtl-weighted hierarchical cox models for snp-set based time-to-event association studies |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502405/ https://www.ncbi.nlm.nih.gov/pubmed/34627275 http://dx.doi.org/10.1186/s12967-021-03090-z |
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