Department of Computer Science and Engineering, IIT Patna, India.
Department of Computer Science and Engineering, IIT Patna, India.
Gene. 2018 Dec 30;679:341-351. doi: 10.1016/j.gene.2018.08.062. Epub 2018 Sep 2.
In recent years DNA microarray technology, leading to the generation of high-volume biological data, has gained significant attention. To analyze this high volume gene-expression data, one such powerful tool is Clustering. For any clustering algorithm, its efficiency majorly depends upon the underlying similarity/dissimilarity measure. During the analysis of such data often there is a need to further explore the similarity of genes not only with respect to their expression values but also with respect to their functional annotations, which can be obtained from Gene Ontology (GO) databases. In the existing literature, several novel clustering and bi-clustering approaches were proposed to identify co-regulated genes from gene-expression datasets. Identifying co-regulated genes from gene expression data misses some important biological information about functionalities of genes, which is necessary to identify semantically related genes. In this paper, we have proposed sixteen different semantic gene-gene dissimilarity measures utilizing biological information of genes retrieved from a global biological database namely Gene Ontology (GO). Four proximity measures, viz. Euclidean, Cosine, point symmetry and line symmetry are utilized along with four different representations of gene-GO-term annotation vectors to develop total sixteen gene-gene dissimilarity measures. In order to illustrate the profitability of developed dissimilarity measures, some multi-objective as well as single-objective clustering algorithms are applied utilizing proposed measures to identify functionally similar genes from Mouse genome and Yeast datasets. Furthermore, we have compared the performance of our proposed sixteen dissimilarity measures with three existing state-of-the-art semantic similarity and distance measures.
近年来,DNA 微阵列技术生成了大量的生物数据,引起了广泛关注。为了分析这些大量的基因表达数据,聚类是一种强大的工具。对于任何聚类算法,其效率主要取决于底层的相似性/相异性度量。在分析此类数据时,通常需要进一步探索基因的相似性,不仅要考虑它们的表达值,还要考虑它们的功能注释,这些注释可以从基因本体论(GO)数据库中获得。在现有文献中,已经提出了几种新的聚类和双聚类方法,用于从基因表达数据集中识别共调控基因。从基因表达数据中识别共调控基因会忽略有关基因功能的一些重要生物学信息,这些信息对于识别语义相关基因是必要的。在本文中,我们提出了十六种不同的语义基因-基因差异度量方法,利用从全球生物数据库(即基因本体论(GO))中检索到的基因生物学信息。利用四种接近度度量方法(即欧几里得、余弦、点对称和线对称)以及四种不同的基因-GO 术语注释向量表示形式,共开发了十六种基因-基因差异度量方法。为了说明开发的差异度量方法的盈利能力,我们应用了一些多目标和单目标聚类算法,利用所提出的方法从鼠基因组和酵母数据集识别功能相似的基因。此外,我们还将我们提出的十六种差异度量方法的性能与三种现有的最先进的语义相似性和距离度量方法进行了比较。