Abstract

Gene Expression Analysis seeks to find the highly expressive genes from a highly dimensional Microarray disease gene Database by using some statistical gene selection approaches based on supervised or unsupervised learning. Gene Ontology (GO) introduces a series of method for annotating gene function that combines semantic similarity measures by taking account on the underlying topology of gene interaction networks for structuring the graphs of the gene ontology. Initially, the genes are identified by clustering microarray disease dataset giving gene id of most expressive genes and further the genes are associated based on their biological functionalities using the gene ontology annotations taken from bioinformatics database. Also, t-test is used for finding the up-regulated genes so it can be annotated to find the most significant gene terms in hierarchical graph structure. The proposed method uses term Similarity measures to compare two or more gene ontology terms. Finally, gene functional classification and gene term association is done by forming a graph structure to be readily analysed by medical practitioner intending the nature of disease-causing genes at deeper level of understanding in chronic disorder based health care environments.

Highlights

  • Gene ontology (GO) has extensive number of techniques and methods for the assuring the biochemical qualities of genes

  • The entire arrangement of gene interaction is used as a Reference Gene Interaction Network (RGIN)

  • RGIN information has been gathered in numerous open databases, for example, the Biomolecular Interaction Network Database (BIND) [3] and Human Genome Gene Ontology Database (HGGODB) [4]

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Summary

Introduction

Gene ontology (GO) has extensive number of techniques and methods for the assuring the biochemical qualities of genes. We utilize a simplest undirected chart, while increasing refined models used guided and named edges to incorporate the data about the sort of biochemical affiliation and its course In this way, the investigation of RGINs requires chart based computational techniques. RGIN information has been gathered in numerous open databases, for example, the Biomolecular Interaction Network Database (BIND) [3] and Human Genome Gene Ontology Database (HGGODB) [4]. These databases are regularly freely accessible on the Internet offering to the client to recover information from basic query interfaces.

Literature Review
GO:009715
Results and Discussion
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