Evidence map›Paper›PMID 31429008›Full record

ArticleGenes & genomics2019

Improving classification accuracy of cancer types using parallel hybrid feature selection on microarray gene expression data.

Lokeswari Venkataramana, Shomona Gracia Jacob, Rajavel Ramadoss, Dodda Saisuma, Dommaraju Haritha, Kunthipuram Manoja

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Article in Genes & genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
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5 citing papers in PubMed.

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6 authors.

Lokeswari VenkataramanaDepartment of CSE, Sri Sivasubramaniya Nadar College of Engineering, Kalavakkam, Chennai, India. lokeswaricts@gmail.com.ORCID 0000-0003-2331-4507
Shomona Gracia Jacob, Muscat, Oman.
Rajavel RamadossDepartment of ECE, Sri Sivasubramaniya Nadar College of Engineering, Kalavakkam, Chennai, India.
Dodda SaisumaDepartment of CSE, Sri Sivasubramaniya Nadar College of Engineering, Kalavakkam, Chennai, India.
Dommaraju HarithaDepartment of CSE, Sri Sivasubramaniya Nadar College of Engineering, Kalavakkam, Chennai, India.
Kunthipuram ManojaDepartment of CSE, Sri Sivasubramaniya Nadar College of Engineering, Kalavakkam, Chennai, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundData mining techniques are used to mine unknown knowledge from huge data. Microarray gene expression (MGE) data plays a major role in predicting type of cancer. But as MGE data is huge in volume, applying traditional data mining approaches is time consuming. Hence parallel programming frameworks like Hadoop, Spark and Mahout are necessary to ease the task of computation.

objectiveNot all the gene expressions are necessary in prediction, it is very essential to select important genes for improving classification accuracy. So feature selection algorithms are parallelized and executed on Spark framework to eliminate unnecessary genes and identify only predictive genes in very less time without affecting prediction accuracy.

methodsParallelized hybrid feature selection (HFS) method is proposed to serve the purpose. This method includes parallelized correlation feature subset selection followed by rank-based feature selection methods. The selected subset of genes is evaluated using parallel classification algorithms. The accuracy values obtained are compared with existing rank-weight feature selection, parallelized recursive feature selection methods and also with the values obtained by executing parallelized HFS on DistributedWekaSpark.

resultsThe classification accuracy obtained with the proposed parallelized HFS method is 97% and 79% for gastric cancer and childhood leukemia respectively. The proposed parallelized HFS method produced ~ 4% to ~ 15% improvement in classification accuracy when compared with previous methods.

conclusionThe results reveal the fact that the proposed parallelized feature selection algorithm is scalable to growing medical data and predicts cancer sub-types in lesser time with higher accuracy.

Indexed as

AlgorithmsBiomarkers, TumorHumansLeukemia, Myeloid, AcuteMicroarray AnalysisMolecular Diagnostic TechniquesSensitivity and SpecificityStomach NeoplasmsBiomarkers, TumorCorrelation feature subset selectionDistributedWekaSparkParallel classificationParallelized hybrid feature selectionRank-based methodsSpark

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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.