通过体细胞突变谱和基因功能信息的集成模型发现潜在的驱动基因

IF 3.743 Q2 Biochemistry, Genetics and Molecular Biology
Jianing Xi, Minghui Wang and Ao Li
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引用次数: 17

摘要

新一代测序数据的积累提供了一个机会,通过计算模型来查明与肿瘤发生有因果关系的驱动基因。尽管之前已经针对这一具有挑战性的问题做出了努力,但在驱动基因识别的准确性方面仍有改进的空间。在本文中,我们提出了一种称为IntDriver的新型集成方法,用于对驱动基因进行优先排序。基于矩阵分解框架,IntDriver可以有效地结合交互网络和基因本体相似度的功能信息,同时检测不同组患者中发生突变的驱动基因。当通过已知的基准驱动基因进行评估时,我们的结果中排名靠前的基因显示出对已知基因的高度显著富集。同时,IntDriver还检测到一些已知的驱动基因,这些基因是其他竞争方法没有发现的。当用精度、召回率和F1分数来衡量时,我们的方法的性能与竞争方法相当或有所提高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Discovering potential driver genes through an integrated model of somatic mutation profiles and gene functional information†

Discovering potential driver genes through an integrated model of somatic mutation profiles and gene functional information†

The accumulating availability of next-generation sequencing data offers an opportunity to pinpoint driver genes that are causally implicated in oncogenesis through computational models. Despite previous efforts made regarding this challenging problem, there is still room for improvement in the driver gene identification accuracy. In this paper, we propose a novel integrated approach called IntDriver for prioritizing driver genes. Based on a matrix factorization framework, IntDriver can effectively incorporate functional information from both the interaction network and Gene Ontology similarity, and detect driver genes mutated in different sets of patients at the same time. When evaluated through known benchmarking driver genes, the top ranked genes of our result show highly significant enrichment for the known genes. Meanwhile, IntDriver also detects some known driver genes that are not found by the other competing approaches. When measured by precision, recall and F1 score, the performances of our approach are comparable or increased in comparison to the competing approaches.

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来源期刊
Molecular BioSystems
Molecular BioSystems 生物-生化与分子生物学
CiteScore
2.94
自引率
0.00%
发文量
0
审稿时长
2.6 months
期刊介绍: Molecular Omics publishes molecular level experimental and bioinformatics research in the -omics sciences, including genomics, proteomics, transcriptomics and metabolomics. We will also welcome multidisciplinary papers presenting studies combining different types of omics, or the interface of omics and other fields such as systems biology or chemical biology.
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