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A Novel Mathematical Approach to Define the Genes/SNPs Conferring Risk or Protection in Sporadic Amyotrophic Lateral Sclerosis Based on Auto Contractive Map Neural Networks and Graph Theory

机译:基于自动收缩图神经网络和图论的散发性肌萎缩性侧索硬化症风险/保护基因/ SNPs定义的新数学方法

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Background. Complex diseases like amyotrophic lateral sclerosis (ALS) implicate phenotypic and genetic heterogeneity. Therefore, multiple genetic traits may show differential association with the disease. The Auto Contractive Map (AutoCM), belonging to the Artificial Neural Network (ANN) architecture, “spatializes” the correlation among variables by constructing a suitable embedding space where a visually transparent and cognitively natural notion such as “closeness” among variables reflects accurately their associations.Results. In this pilot case-control study single nucleotide polymorphism (SNP) in several genes has been evaluated with a novel data mining approach based on an AutoCM. We have divided the ALS dataset into two dataset: Cases and Control dataset; we have applied to each one, independently, the AutoCM algorithm. Six genetic variants were identified which differently contributed to the complexity of the system: three of the above genes/SNPs represent protective factors, APOA4, NOS3, and LPL, since their contribution to the whole complexity resulted to be as high as 0.17. On the other hand ADRB3, LIPC, and MMP3, whose hub relevancies contribution resulted to be as high as 0.13, seem to represent susceptibility factors.Conclusion. The biological information available on these six polymorphisms is consistent with possible pathogenetic pathways related to ALS.
机译:背景。肌萎缩性侧索硬化症(ALS)等复杂疾病牵涉到表型和遗传异质性。因此,多种遗传性状可能显示出与疾病的不同关联。属于人工神经网络(ANN)架构的自动收缩图(AutoCM)通过构建合适的嵌入空间来“空间化”变量之间的相关性,在该嵌入空间中,变量之间的“透明”等视觉透明和认知自然的概念可以准确地反映变量关联。结果。在这项先导病例对照研究中,已经使用基于AutoCM的新型数据挖掘方法评估了多个基因中的单核苷酸多态性(SNP)。我们将ALS数据集分为两个数据集:Cases和Control数据集;我们已经将AutoCM算法独立地应用于每个算法。确定了六个遗传变异,这些变异对系统的复杂性有不同的贡献:上述基因/ SNP中的三个代表保护因子APOA4,NOS3和LPL,因为它们对整个复杂性的贡献高达0.17。另一方面,ADRB3,LIPC和MMP3的枢纽相关性贡献高达0.13,似乎代表了敏感性因素。有关这六个多态性的生物学信息与与ALS相关的可能的致病途径一致。

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