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SMetABF:一种快速算法,用于包含大量研究的贝叶斯 GWAS 荟萃分析。

SMetABF: A rapid algorithm for Bayesian GWAS meta-analysis with a large number of studies included.

机构信息

Department of Bioinformatics and Biostatistics, School of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.

Department of Biostatistics, Nanjing Medical University School of Public Health, Nanjing, Jiangsu, China.

出版信息

PLoS Comput Biol. 2022 Mar 14;18(3):e1009948. doi: 10.1371/journal.pcbi.1009948. eCollection 2022 Mar.

DOI:10.1371/journal.pcbi.1009948
PMID:35286307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8947622/
Abstract

Bayesian methods are widely used in the GWAS meta-analysis. But the considerable consumption in both computing time and memory space poses great challenges for large-scale meta-analyses. In this research, we propose an algorithm named SMetABF to rapidly obtain the optimal ABF in the GWAS meta-analysis, where shotgun stochastic search (SSS) is introduced to improve the Bayesian GWAS meta-analysis framework, MetABF. Simulation studies confirm that SMetABF performs well in both speed and accuracy, compared to exhaustive methods and MCMC. SMetABF is applied to real GWAS datasets to find several essential loci related to Parkinson's disease (PD) and the results support the underlying relationship between PD and other autoimmune disorders. Developed as an R package and a web tool, SMetABF will become a useful tool to integrate different studies and identify more variants associated with complex traits.

摘要

贝叶斯方法广泛应用于 GWAS 荟萃分析。但是,在计算时间和内存空间方面的大量消耗给大规模荟萃分析带来了巨大的挑战。在这项研究中,我们提出了一种名为 SMetABF 的算法,用于在 GWAS 荟萃分析中快速获得最优 ABF,其中引入了散弹式随机搜索(SSS)来改进贝叶斯 GWAS 荟萃分析框架 MetABF。模拟研究证实,与穷举法和 MCMC 相比,SMetABF 在速度和准确性方面表现良好。SMetABF 应用于真实的 GWAS 数据集,以发现与帕金森病(PD)相关的几个重要基因座,结果支持 PD 与其他自身免疫性疾病之间的潜在关系。作为一个 R 包和一个网络工具开发,SMetABF 将成为整合不同研究和识别与复杂性状相关的更多变体的有用工具。

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本文引用的文献

1
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Nat Genet. 2021 Nov;53(11):1616-1621. doi: 10.1038/s41588-021-00954-4. Epub 2021 Nov 4.
2
Exome sequencing and analysis of 454,787 UK Biobank participants.外显子组测序和分析 454787 名英国生物银行参与者。
Nature. 2021 Nov;599(7886):628-634. doi: 10.1038/s41586-021-04103-z. Epub 2021 Oct 18.
3
A cross-population atlas of genetic associations for 220 human phenotypes.220 个人类表型的跨人群遗传关联图谱。
基于贝叶斯网络的孟德尔随机化用于变异优先级排序和表型因果推断。
Hum Genet. 2024 Oct;143(9-10):1081-1094. doi: 10.1007/s00439-024-02640-x. Epub 2024 Feb 21.
4
STS-BN: An efficient Bayesian network method for detecting causal SNPs.STS-BN:一种用于检测因果单核苷酸多态性的高效贝叶斯网络方法。
Front Genet. 2022 Sep 15;13:942464. doi: 10.3389/fgene.2022.942464. eCollection 2022.
Nat Genet. 2021 Oct;53(10):1415-1424. doi: 10.1038/s41588-021-00931-x. Epub 2021 Sep 30.
4
GESLM algorithm for detecting causal SNPs in GWAS with multiple phenotypes.用于检测具有多种表型的 GWAS 中因果 SNPs 的 GESLM 算法。
Brief Bioinform. 2021 Nov 5;22(6). doi: 10.1093/bib/bbab276.
5
Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank.利用英国生物银行研究抑郁症与自身免疫性疾病之间的多效性
Biol Psychiatry Glob Open Sci. 2021 Jun;1(1):48-58. doi: 10.1016/j.bpsgos.2021.03.002.
6
Imputation and Reanalysis of ExomeChip Data Identifies Novel, Conditional and Joint Genetic Effects on Parkinson's Disease Risk.外显子芯片数据的推断和重新分析确定了帕金森病风险的新的、条件性的和联合遗传效应。
Genes (Basel). 2021 May 4;12(5):689. doi: 10.3390/genes12050689.
7
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Neurol Genet. 2021 Jan 28;7(2):e557. doi: 10.1212/NXG.0000000000000557. eCollection 2021 Apr.
8
Common genetic associations between age-related diseases.与年龄相关疾病的常见遗传关联。
Nat Aging. 2021 Apr;1(4):400-412. doi: 10.1038/s43587-021-00051-5. Epub 2021 Apr 8.
9
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Nat Commun. 2021 Feb 19;12(1):1146. doi: 10.1038/s41467-021-21280-7.
10
Analysis in epithelial ovarian cancer identifies KANSL1 as a biomarker and target gene for immune response and HDAC inhibition.在卵巢上皮癌分析中,KANSL1 被鉴定为免疫反应和 HDAC 抑制的生物标志物和靶基因。
Gynecol Oncol. 2021 Feb;160(2):539-546. doi: 10.1016/j.ygyno.2020.11.008. Epub 2020 Nov 20.