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首页> 外文期刊>BMC Bioinformatics >iMEGES: integrated mental-disorder GEnome score by deep neural network for prioritizing the susceptibility genes for mental disorders in personal genomes
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iMEGES: integrated mental-disorder GEnome score by deep neural network for prioritizing the susceptibility genes for mental disorders in personal genomes

机译:IMeges:深神经网络综合精神障碍基因组评分,以优先考虑个人基因组中精神障碍的敏感性基因

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摘要

A range of rare and common genetic variants have been discovered to be potentially associated with mental diseases, but many more have not been uncovered. Powerful integrative methods are needed to systematically prioritize both variants and genes that confer susceptibility to mental diseases in personal genomes of individual patients and to facilitate the development of personalized treatment or therapeutic approaches. Leveraging deep neural network on the TensorFlow framework, we developed a computational tool, integrated Mental-disorder GEnome Score (iMEGES), for analyzing whole genome/exome sequencing data on personal genomes. iMEGES takes as input genetic mutations and phenotypic information from a patient with mental disorders, and outputs the rank of whole genome susceptibility variants and the prioritized disease-specific genes for mental disorders by integrating contributions from coding and non-coding variants, structural variants (SVs), known brain expression quantitative trait loci (eQTLs), and epigenetic information from PsychENCODE. iMEGES was evaluated on multiple datasets of mental disorders, and it achieved improved performance than competing approaches when large training dataset is available. iMEGES can be used in population studies to help the prioritization of novel genes or variants that might be associated with the susceptibility to mental disorders, and also on individual patients to help the identification of genes or variants related to mental diseases.
机译:已经发现一系列罕见和常见的遗传变异可能与精神疾病有可能与精神疾病相关,但更多尚未被发现。需要强大的综合方法来系统地优先考虑赋予个体患者个人基因组易患精神疾病的变体和基因,并促进个性化待遇或治疗方法的发展。利用深度神经网络对Tensorflow框架,我们开发了一种计算工具,综合精神障碍基因组评分(IMEGES),用于分析个人基因组上的全基因组/外壳测序数据。 IMeges作为输入基因突变和来自精神障碍的患者的表型信息,并通过整合来自编码和非编码变体,结构变体(SV)的贡献来输出整个基因组易感变体和优先疾病特异性基因的级别疾病的等级),已知的大脑表达量化性状基因座(EQTLS)以及来自Phangencendode的表观信息。在精神障碍的多个数据集上评估了IMEGES,并且在大型训练数据集可用时,它会实现的性能而不是竞争方法。 IMeges可用于人口研究,以帮助优先考虑可能与精神障碍易感性相关的新型基因或变体,以及个体患者,以帮助鉴定与精神疾病有关的基因或变体。

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