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A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization
BACKGROUND: Autism spectrum disorder (ASD) is a group of complex neurodevelopment disorders with a strong genetic basis. Large scale sequencing studies have identified over one hundred ASD risk genes. Nevertheless, the vast majority of ASD risk genes remain to be discovered, as it is estimated that...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034518/ https://www.ncbi.nlm.nih.gov/pubmed/35459094 http://dx.doi.org/10.1186/s12859-022-04616-y |
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author | Ji, Ying Chen, Rui Wang, Quan Wei, Qiang Tao, Ran Li, Bingshan |
author_facet | Ji, Ying Chen, Rui Wang, Quan Wei, Qiang Tao, Ran Li, Bingshan |
author_sort | Ji, Ying |
collection | PubMed |
description | BACKGROUND: Autism spectrum disorder (ASD) is a group of complex neurodevelopment disorders with a strong genetic basis. Large scale sequencing studies have identified over one hundred ASD risk genes. Nevertheless, the vast majority of ASD risk genes remain to be discovered, as it is estimated that more than 1000 genes are likely to be involved in ASD risk. Prioritization of risk genes is an effective strategy to increase the power of identifying novel risk genes in genetics studies of ASD. As ASD risk genes are likely to exhibit distinct properties from multiple angles, we reason that integrating multiple levels of genomic data is a powerful approach to pinpoint genuine ASD risk genes. RESULTS: We present BNScore, a Bayesian model selection framework to probabilistically prioritize ASD risk genes through explicitly integrating evidence from sequencing-identified ASD genes, biological annotations, and gene functional network. We demonstrate the validity of our approach and its improved performance over existing methods by examining the resulting top candidate ASD risk genes against sets of high-confidence benchmark genes and large-scale ASD genome-wide association studies. We assess the tissue-, cell type- and development stage-specific expression properties of top prioritized genes, and find strong expression specificity in brain tissues, striatal medium spiny neurons, and fetal developmental stages. CONCLUSIONS: In summary, we show that by integrating sequencing findings, functional annotation profiles, and gene-gene functional network, our proposed BNScore provides competitive performance compared to current state-of-the-art methods in prioritizing ASD genes. Our method offers a general and flexible strategy to risk gene prioritization that can potentially be applied to other complex traits as well. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-022-04616-y. |
format | Online Article Text |
id | pubmed-9034518 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-90345182022-04-24 A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization Ji, Ying Chen, Rui Wang, Quan Wei, Qiang Tao, Ran Li, Bingshan BMC Bioinformatics Research BACKGROUND: Autism spectrum disorder (ASD) is a group of complex neurodevelopment disorders with a strong genetic basis. Large scale sequencing studies have identified over one hundred ASD risk genes. Nevertheless, the vast majority of ASD risk genes remain to be discovered, as it is estimated that more than 1000 genes are likely to be involved in ASD risk. Prioritization of risk genes is an effective strategy to increase the power of identifying novel risk genes in genetics studies of ASD. As ASD risk genes are likely to exhibit distinct properties from multiple angles, we reason that integrating multiple levels of genomic data is a powerful approach to pinpoint genuine ASD risk genes. RESULTS: We present BNScore, a Bayesian model selection framework to probabilistically prioritize ASD risk genes through explicitly integrating evidence from sequencing-identified ASD genes, biological annotations, and gene functional network. We demonstrate the validity of our approach and its improved performance over existing methods by examining the resulting top candidate ASD risk genes against sets of high-confidence benchmark genes and large-scale ASD genome-wide association studies. We assess the tissue-, cell type- and development stage-specific expression properties of top prioritized genes, and find strong expression specificity in brain tissues, striatal medium spiny neurons, and fetal developmental stages. CONCLUSIONS: In summary, we show that by integrating sequencing findings, functional annotation profiles, and gene-gene functional network, our proposed BNScore provides competitive performance compared to current state-of-the-art methods in prioritizing ASD genes. Our method offers a general and flexible strategy to risk gene prioritization that can potentially be applied to other complex traits as well. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-022-04616-y. BioMed Central 2022-04-22 /pmc/articles/PMC9034518/ /pubmed/35459094 http://dx.doi.org/10.1186/s12859-022-04616-y 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 Ji, Ying Chen, Rui Wang, Quan Wei, Qiang Tao, Ran Li, Bingshan A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization |
title | A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization |
title_full | A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization |
title_fullStr | A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization |
title_full_unstemmed | A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization |
title_short | A Bayesian framework to integrate multi-level genome-scale data for Autism risk gene prioritization |
title_sort | bayesian framework to integrate multi-level genome-scale data for autism risk gene prioritization |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9034518/ https://www.ncbi.nlm.nih.gov/pubmed/35459094 http://dx.doi.org/10.1186/s12859-022-04616-y |
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