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Gene Mutation Analysis for Functional Annotations Using Graph Heuristics

机译:使用图启发式进行功能注释的基因突变分析

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Research studies on pathogenic mutations are important and beneficial for understanding disease development, prognosis and gene-disease associations. Moreover, pathogenic mutations have harmful consequences which may lead to certain diseases or medical conditions. This paper presents a method for inducing the most significant and accurate functions for a given set of mutations having one common aspect, e.g. specific disease. The proposed method is based on the directed acyclic graph of the gene ontology to identify the most significant least common subsumers to be used for functionally annotating the mutations under investigation. We applied the method on a large sets of mutations. The reported results in this paper are encouraging and suggest that a mutation can have, and can be annotated with a function, e.g. biological process, from the gene ontology just like the genes, which contributes into a more complete understanding of mutation pathogenicity, mutation-gene-disease relationships, and disease mechanisms.
机译:对致病突变的研究对于理解疾病的发展,预后和基因-疾病关联具有重要意义。此外,致病突变具有有害后果,可能导致某些疾病或医疗状况。本文提出了一种方法,可以针对一组具有一个共同方面,例如基因突变的给定突变,诱导出最重要,最准确的功能。特定疾病。所提出的方法基于基因本体论的有向无环图,以识别将用于功能上注释研究突变的最重要的最不常见的使用者。我们将该方法应用于大量突变。该论文报道的结果令人鼓舞,并暗示突变可以具有,并可以用例如下列的功能注释。就像基因一样,从基因本体论出发,从生物学过程来看,这有助于更全面地了解突变的致病性,突变与基因-疾病的关系以及疾病的机理。

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