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Semantic Disease Gene Embeddings (SmuDGE): phenotype-based disease gene prioritization without phenotypes

机译:语义疾病基因嵌入(SmuDGE):无表型的基于表型的疾病基因优先排序

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摘要

MotivationIn the past years, several methods have been developed to incorporate information about phenotypes into computational disease gene prioritization methods. These methods commonly compute the similarity between a disease’s (or patient’s) phenotypes and a database of gene-to-phenotype associations to find the phenotypically most similar match. A key limitation of these methods is their reliance on knowledge about phenotypes associated with particular genes which is highly incomplete in humans as well as in many model organisms such as the mouse.
机译:动机在过去的几年中,已经开发出了几种方法来将有关表型的信息纳入计算疾病基因的优先排序方法。这些方法通常计算疾病(或患者)表型与基因表型关联数据库之间的相似度,以找到表型上最相似的匹配。这些方法的关键局限性在于它们依赖于与特定基因相关的表型的知识,这些知识在人类以及许多模型生物(如小鼠)中都是高度不完整的。

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