Evidence map›Paper›PMID 21326602›Full record

ArticlePloS one2011

Optimization based tumor classification from microarray gene expression data.

Onur Dagliyan, Fadime Uney-Yuksektepe, I Halil Kavakli, Metin Turkay

Abstract readEvaluation Study
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

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0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

  1. Review
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  10. Copy number variation analysis based on AluScan sequences.Journal of clinical bioinformatics · 2014
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Onur DagliyanDepartment of Chemical and Biological Engineering, Koc University, Istanbul, Turkey.
Fadime Uney-Yuksektepe
I Halil Kavakli
Metin Turkay

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAn important use of data obtained from microarray measurements is the classification of tumor types with respect to genes that are either up or down regulated in specific cancer types. A number of algorithms have been proposed to obtain such classifications. These algorithms usually require parameter optimization to obtain accurate results depending on the type of data. Additionally, it is highly critical to find an optimal set of markers among those up or down regulated genes that can be clinically utilized to build assays for the diagnosis or to follow progression of specific cancer types. In this paper, we employ a mixed integer programming based classification algorithm named hyper-box enclosure method (HBE) for the classification of some cancer types with a minimal set of predictor genes. This optimization based method which is a user friendly and efficient classifier may allow the clinicians to diagnose and follow progression of certain cancer types. METHODOLOGY/PRINCIPAL

findingsWe apply HBE algorithm to some well known data sets such as leukemia, prostate cancer, diffuse large B-cell lymphoma (DLBCL), small round blue cell tumors (SRBCT) to find some predictor genes that can be utilized for diagnosis and prognosis in a robust manner with a high accuracy. Our approach does not require any modification or parameter optimization for each data set. Additionally, information gain attribute evaluator, relief attribute evaluator and correlation-based feature selection methods are employed for the gene selection. The results are compared with those from other studies and biological roles of selected genes in corresponding cancer type are described. CONCLUSIONS/SIGNIFICANCE: The performance of our algorithm overall was better than the other algorithms reported in the literature and classifiers found in WEKA data-mining package. Since it does not require a parameter optimization and it performs consistently very high prediction rate on different type of data sets, HBE method is an effective and consistent tool for cancer type prediction with a small number of gene markers.

Indexed as

AlgorithmsCalibrationElectronic Data ProcessingGene Expression ProfilingGene Expression Regulation, NeoplasticHumansLeukemiaLymphoma, Large B-Cell, DiffuseMaleMicroarray AnalysisModels, TheoreticalNeoplasmsPattern Recognition, AutomatedPrognosisProstatic Neoplasms

Identifiers

PMID21326602
PMCPMC3033885

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.