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Guilt-by association approach to identify novel human aging-related genes using protein domains

机译:内关联法使用蛋白质结构域识别新的人类衰老相关基因

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Elucidating the genetic reasons associated with aging and longevity could greatly help in designing strategies to extend years of healthy life in humans. Extensive studies have been carried out in model organisms to find the effect of genes on aging. Understandably, human aging is difficult to research due to the complexity of the processes involved in aging, along with the time and ethical constraints associated with the human life. In spite of these constraints, the Human Ageing Genomic Resources (HAGR) has compiled the GenAge database, a curated list of aging related genes in humans and model organisms using information from published literature. We hypothesized that biological feature-based data mining approaches can overcome the existing limitations associated with human aging research. In this study we develop a computational method to identify aging related human genes that may play a potential role in aging and life span related processes. We employed protein domain information and guilt-by association approach to predict potential aging related genes, which resulted into the identification of twenty-seven novel human aging related genes.
机译:阐明与老化和长寿相关的遗传原因可以极大地帮助设计延长人类健康生活的策略。在模型生物中进行了广泛的研究,以找到基因对老化的影响。可以理解的是,由于衰老的过程的复杂性以及与人类生命相关的时间和道德限制,难以研究人类老龄化。尽管有这些约束,人类老化基因组资源(HAGR)已经编制了Genage数据库,使用来自文献中发表的信息的信息和模型生物体中的老化相关基因的策划列表。我们假设基于生物学特征的数据挖掘方法可以克服与人类老化研究相关的现有限制。在该研究中,我们开发了一种计算方法,以鉴定可能在老化和生命跨度相关过程中发挥潜在作用的衰老相关人类基因。我们使用蛋白质结构域信息和内疚,通过关联方法来预测潜在的老化相关基因,这导致鉴定了二十七种新的人衰老相关基因。

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