AI Article Synopsis

  • Scientists are looking for ways to improve how they group gene data by using extra information, like Gene Ontology (GO) labels, to make the groupings more meaningful.
  • They created a new algorithm that combines knowledge from GO structure with methods for grouping genes based on their activity, making it better at handling different types of gene labels.
  • Their algorithm showed better results than older methods, especially in identifying important groups of genes related to things like the immune system and how the body processes sugar, which are backed up by additional data.

Article Abstract

Motivation: There is a growing interest in improving the cluster analysis of expression data by incorporating into it prior knowledge, such as the Gene Ontology (GO) annotations of genes, in order to improve the biological relevance of the clusters that are subjected to subsequent scrutiny. The structure of the GO is another source of background knowledge that can be exploited through the use of semantic similarity.

Results: We propose here a novel algorithm that integrates semantic similarities (derived from the ontology structure) into the procedure of deriving clusters from the dendrogram constructed during expression-based hierarchical clustering. Our approach can handle the multiple annotations, from different levels of the GO hierarchy, which most genes have. Moreover, it treats annotated and unannotated genes in a uniform manner. Consequently, the clusters obtained by our algorithm are characterized by significantly enriched annotations. In both cross-validation tests and when using an external index such as protein-protein interactions, our algorithm performs better than previous approaches. When applied to human cancer expression data, our algorithm identifies, among others, clusters of genes related to immune response and glucose metabolism. These clusters are also supported by protein-protein interaction data.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2705235PMC
http://dx.doi.org/10.1093/bioinformatics/btp327DOI Listing

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