基于ld的深度学习用于WGS数据的阿尔茨海默病基因位点检测。

Taeho Jo, Paula Bice, Kwangsik Nho, Andrew J. Saykin, Alzheimer's Disease Sequencing Project
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引用次数: 0

摘要

基因组数据集的指数级增长需要先进的分析工具来有效地从大规模高通量测序数据中识别遗传位点。本研究提出了deep - block,这是一个多阶段深度学习框架,将生物学知识纳入其人工智能架构,以识别与阿尔茨海默病(AD)显著相关的遗传区域。该框架采用三阶段方法:(1)基于连锁不平衡(LD)模式的基因组分割,(2)利用稀疏注意机制选择相关LD块,以及(3)应用TabNet和Random Forest算法量化单核苷酸多态性(SNP)特征重要性,从而确定导致AD风险的遗传因素。方法:Deep-Block应用于来自阿尔茨海默病测序项目(ADSP)的大规模全基因组测序(WGS)数据集,包括7416名非西班牙裔白人(NHW)参与者(3150名认知正常的老年人(CN), 4266名AD)。结果:30,218个LD块被确定,然后根据它们与阿尔茨海默病的相关性进行排名。随后,Deep-Block在前1500个LD块中发现了新的snp,并确认了以前已知的变体,包括APOE rs429358和rs769449。跨13个脑区的表达数量性状位点(eQTL)分析为鉴定的变异提供了功能证据。将结果与欧洲阿尔茨海默病和痴呆症生物银行(EADB)和GWAS目录中已建立的ad相关基因座进行交叉验证。讨论:Deep-Block框架有效地处理大规模高通量测序数据,同时在降维过程中保留SNP相互作用,最大限度地减少偏差和信息损失。该框架的发现得到了跨大脑区域的组织特异性eQTL证据的支持,表明了已识别变体的功能相关性。此外,Deep-Block方法已经确定了已知和新的遗传变异,增强了我们对遗传结构的理解,并展示了其在大规模测序研究中的应用潜力。亮点:不断增长的基因组数据集需要先进的工具来识别测序中的遗传位点。采用一种新的人工智能框架Deep-Block对大规模ADSP WGS数据进行处理。Deep-Block发现了已知的和新的ad相关基因位点。rs429358 (APOE)是关键;rs11556505 (TOMM40)、rs34342646 (NECTIN2)具有显著性。人工智能框架利用生物学知识来加强对阿尔茨海默氏症基因位点的检测。
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LD-informed deep learning for Alzheimer's gene loci detection using WGS data

INTRODUCTION

The exponential growth of genomic datasets necessitates advanced analytical tools to effectively identify genetic loci from large-scale high throughput sequencing data. This study presents Deep-Block, a multi-stage deep learning framework that incorporates biological knowledge into its AI architecture to identify genetic regions as significantly associated with Alzheimer's disease (AD). The framework employs a three-stage approach: (1) genome segmentation based on linkage disequilibrium (LD) patterns, (2) selection of relevant LD blocks using sparse attention mechanisms, and (3) application of TabNet and Random Forest algorithms to quantify single nucleotide polymorphism (SNP) feature importance, thereby identifying genetic factors contributing to AD risk.

METHODS

The Deep-Block was applied to a large-scale whole genome sequencing (WGS) dataset from the Alzheimer's Disease Sequencing Project (ADSP), comprising 7416 non-Hispanic white (NHW) participants (3150 cognitively normal older adults (CN), 4266 AD).

RESULTS

30,218 LD blocks were identified and then ranked based on their relevance with Alzheimer's disease. Subsequently, the Deep-Block identified novel SNPs within the top 1500 LD blocks and confirmed previously known variants, including APOE rs429358 and rs769449. Expression Quantitative Trait Loci (eQTL) analysis across 13 brain regions provided functional evidence for the identified variants. The results were cross-validated against established AD-associated loci from the European Alzheimer's and Dementia Biobank (EADB) and the GWAS catalog.

DISCUSSION

The Deep-Block framework effectively processes large-scale high throughput sequencing data while preserving SNP interactions during dimensionality reduction, minimizing bias and information loss. The framework's findings are supported by tissue-specific eQTL evidence across brain regions, indicating the functional relevance of the identified variants. Additionally, the Deep-Block approach has identified both known and novel genetic variants, enhancing our understanding of the genetic architecture and demonstrating its potential for application in large-scale sequencing studies.

Highlights

  • Growing genomic datasets require advanced tools to identify genetic loci in sequencing.
  • Deep-Block, a novel AI framework, was used to process large-scale ADSP WGS data.
  • Deep-Block identified both known and novel AD-associated genetic loci.
  • rs429358 (APOE) was key; rs11556505 (TOMM40), rs34342646 (NECTIN2) were significant.
  • The AI framework uses biological knowledge to enhance detection of Alzheimer's loci.
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来源期刊
CiteScore
10.10
自引率
2.10%
发文量
134
审稿时长
10 weeks
期刊介绍: Alzheimer''s & Dementia: Translational Research & Clinical Interventions (TRCI) is a peer-reviewed, open access,journal from the Alzheimer''s Association®. The journal seeks to bridge the full scope of explorations between basic research on drug discovery and clinical studies, validating putative therapies for aging-related chronic brain conditions that affect cognition, motor functions, and other behavioral or clinical symptoms associated with all forms dementia and Alzheimer''s disease. The journal will publish findings from diverse domains of research and disciplines to accelerate the conversion of abstract facts into practical knowledge: specifically, to translate what is learned at the bench into bedside applications. The journal seeks to publish articles that go beyond a singular emphasis on either basic drug discovery research or clinical research. Rather, an important theme of articles will be the linkages between and among the various discrete steps in the complex continuum of therapy development. For rapid communication among a multidisciplinary research audience involving the range of therapeutic interventions, TRCI will consider only original contributions that include feature length research articles, systematic reviews, meta-analyses, brief reports, narrative reviews, commentaries, letters, perspectives, and research news that would advance wide range of interventions to ameliorate symptoms or alter the progression of chronic neurocognitive disorders such as dementia and Alzheimer''s disease. The journal will publish on topics related to medicine, geriatrics, neuroscience, neurophysiology, neurology, psychiatry, clinical psychology, bioinformatics, pharmaco-genetics, regulatory issues, health economics, pharmacoeconomics, and public health policy as these apply to preclinical and clinical research on therapeutics.
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