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通过亚细胞定位数据与蛋白质-蛋白质相互作用网络的整合进行乳腺癌候选基因检测。

Breast Cancer Candidate Gene Detection Through Integration of Subcellular Localization Data With Protein-Protein Interaction Networks.

出版信息

IEEE Trans Nanobioscience. 2020 Jul;19(3):556-561. doi: 10.1109/TNB.2020.2990178. Epub 2020 Apr 24.

Abstract

Due to technological advances the quality and availability of biological data has increased dramatically in the last decade. Analysing protein-protein interaction networks (PPINs) in an integrated way, together with subcellular compartment data, provides such biological context, helps to fill in the gaps between a single type of biological data and genes causing diseases and can identify novel genes related to disease. In this study, we present BCCGD, a method for integrating subcellular localization data with PPINs that detects breast cancer candidate genes in protein complexes. We achieve this by defining the significance of the compartment, constructing edge-weighted PPINs, finding protein complexes with a non-negative matrix factorization approach, generating disease-specific networks based on the known disease genes, prioritizing disease candidate genes with a WDC method. As a case study, we investigate the breast cancer but the techniques described here are applicable to other disorders. For the top genes scored by BCCGD approach, we utilize the literature retrieving method to test the correlations of them with the breast cancer. The results show that BCCGD discover some novel breast cancer candidate genes which are valuable references for the biomedical scientists.

摘要

由于技术的进步,过去十年中生物数据的质量和可用性有了显著提高。以综合的方式分析蛋白质-蛋白质相互作用网络 (PPIN) 以及亚细胞区室数据,可以提供这种生物学背景,有助于填补单一类型生物数据与导致疾病的基因之间的空白,并可以识别与疾病相关的新基因。在这项研究中,我们提出了 BCCGD,这是一种将亚细胞定位数据与 PPIN 集成的方法,用于检测蛋白质复合物中的乳腺癌候选基因。我们通过定义区室的重要性、构建带权 PPIN、使用非负矩阵分解方法找到蛋白质复合物、基于已知疾病基因生成特定疾病的网络、使用 WDC 方法对疾病候选基因进行优先级排序来实现这一目标。作为一个案例研究,我们研究了乳腺癌,但这里描述的技术适用于其他疾病。对于 BCCGD 方法评分最高的基因,我们利用文献检索方法测试它们与乳腺癌的相关性。结果表明,BCCGD 发现了一些新的乳腺癌候选基因,这对生物医学科学家来说是有价值的参考。

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