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A Hybrid Clustering Algorithm and Functional Study of Gene Expression in Lung Adenocarcinoma

机译:肺腺癌基因表达的杂种聚类算法与功能研究

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DNA Microarray technology provides a convenient way to investigate expression levels of thousands of genes in a collection of related samples during different biological processes. Researchers from diverse disciplines such as computer science and biology have found it interesting as well as meaningful to group genes based on the similarity of their expression patterns. Hierarchical clustering and k-means clustering are commonly used algorithms to group genes with similar expression patterns. However, in spite of having some advantages such as producing tighter cluster than other algorithms, k-means clustering has some limitations also. The performance of k-means clustering algorithm largely depends on the selection of the value of k i.e., the number of clusters. In this research work, we proposed a new method to combine k-means clustering with hierarchical clustering to overcome the limitation. To test the algorithm, we used microarray data on lung adenocarcinoma, the most common type of non-small-cell cancers. We identified a number of representative genes from the group of normal tissue and from the group of KRAS mutation tissues. Genes for both of these groups were clustered using our proposed method. Finally we conducted functional investigation of the differentially expressed genes using Gene Ontology database to find changes in the enrichment of molecular functions of the genes contained in each cluster of both normal and KRAS positive groups. We discovered that our proposed method can group genes with similar expression pattern together and hence it can be used in future for clustering microarray data.
机译:DNA微阵列技术提供了一种方便的方法来研究在不同的生物过程中探讨相关样品的集合中成千上万基因的表达水平。来自计算机科学和生物学等多种学科的研究人员发现,基于其表达式模式的相似性,对组基因有趣并有意义。分层聚类和k-means群集是常用算法到具有类似表达模式的组基因。然而,尽管具有一些优点,例如产生比其他算法的更严格的簇,但K-Means聚类也有一些限制。 K-Means聚类算法的性能很大程度上取决于选择K即的值,簇的数量。在这项研究工作中,我们提出了一种将K-Means群集与分层聚类组合的新方法来克服限制。为了测试算法,我们使用肺腺癌的微阵列数据,最常见的非小细胞癌。我们鉴定了来自正常组织组和来自KRAS突变组织组的许多代表性基因。使用我们所提出的方法对这些组的两组基因进行聚类。最后,我们使用基因本体数据库对差异表达基因进行了功能性研究,以找到正常和KRAS阳性基团中含有的基因分子函数的富集的变化。我们发现我们所提出的方法可以将具有类似表达模式的基因组在一起,因此可以将来用于聚类微阵列数据。

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