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Showing papers by "Volkan Atalay published in 2010"


Journal ArticleDOI
31 Aug 2010-PLOS ONE
TL;DR: This study formulated the function annotation problem as a classification problem defined on 300 different Gene Ontology (GO) terms from molecular function aspect, and applied three different methods and their combinations.
Abstract: Functional protein annotation is an important matter for in vivo and in silico biology. Several computational methods have been proposed that make use of a wide range of features such as motifs, domains, homology, structure and physicochemical properties. There is no single method that performs best in all functional classification problems because information obtained using any of these features depends on the function to be assigned to the protein. In this study, we portray a novel approach that combines different methods to better represent protein function. First, we formulated the function annotation problem as a classification problem defined on 300 different Gene Ontology (GO) terms from molecular function aspect. We presented a method to form positive and negative training examples while taking into account the directed acyclic graph (DAG) structure and evidence codes of GO. We applied three different methods and their combinations. Results show that combining different methods improves prediction accuracy in most cases. The proposed method, GOPred, is available as an online computational annotation tool (http://kinaz.fen.bilkent.edu.tr/gopred).

26 citations


Journal ArticleDOI
01 Dec 2010
TL;DR: A novel framework, bi-k-bi clustering, for finding association rules of gene pairs that can easily operate on large scale and multiple heterogeneous data sets is proposed and applied on the available NCBI GEO Homo sapiens data sets.
Abstract: Due to the increase in gene expression data sets in recent years, various data mining techniques have been proposed for mining gene expression profiles. However, most of these methods target single gene expression data sets and cannot handle all the available gene expression data in public databases in reasonable amount of time and space. In this paper, we propose a novel framework, bi-k-bi clustering, for finding association rules of gene pairs that can easily operate on large scale and multiple heterogeneous data sets. We applied our proposed framework on the available NCBI GEO Homo sapiens data sets. Our results show consistency and relatedness with the available literature and also provides novel associations.

4 citations


DOI
01 Jan 2010
TL;DR: In this article, the authors combined the ChIP-seq and the transcriptome data and integrated these data into signaling cascades through a framework based on data-and model-driven hybrid approach.
Abstract: In this study, we combined the ChIP-seq and the transcriptome data and integrated these data into signaling cascades. Integration was realized through a framework based on data- and model-driven hybrid approach. An enrichment model was constructed to evaluate signaling cascades which resulted in specic cellular processes. We used ChIP-seq and microarray data from public databases which were obtained from HeLa cells under oxidative stress having similar experimental setups. Both ChIP-seq and array data were analyzed by percentile ranking for the sake of simultaneous data integration on specic genes. Signaling cascades from KEGG pathway database were subsequently scored by taking sum of the individual scores of the genes involved within the cascade. This scoring information is then transferred to en route of the signaling cascade to form the nal score. Signaling cascade model based framework that we describe in this study is a novel approach which calculates scores for the target process of the analyzed signaling cascade, rather than assigning scores to gene product nodes.

1 citations