Evidence map›Paper›PMID 30228989›Full record

ArticleBioMed research international2018

An Efficient Feature Selection Strategy Based on Multiple Support Vector Machine Technology with Gene Expression Data.

Ying Zhang, Qingchun Deng, Wenbin Liang, Xianchun Zou

Abstract read
In one paragraph

Article in BioMed research international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Ying ZhangCollege of Computer and Information Science, Southwest University, Chongqing 400715, China.ORCID 0000-0002-7688-7918
Qingchun DengDepartment of Gynecology and Obstetrics (Southwest Hospital), Third Military Medical University, Chongqing 400038, China.
Wenbin LiangKey Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China.
Xianchun ZouCollege of Computer and Information Science, Southwest University, Chongqing 400715, China.ORCID 0000-0001-6058-4069

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The application of gene expression data to the diagnosis and classification of cancer has become a hot issue in the field of cancer classification. Gene expression data usually contains a large number of tumor-free data and has the characteristics of high dimensions. In order to select determinant genes related to breast cancer from the initial gene expression data, we propose a new feature selection method, namely, support vector machine based on recursive feature elimination and parameter optimization (SVM-RFE-PO). The grid search (GS) algorithm, the particle swarm optimization (PSO) algorithm, and the genetic algorithm (GA) are applied to search the optimal parameters in the feature selection process. Herein, the new feature selection method contains three kinds of algorithms: support vector machine based on recursive feature elimination and grid search (SVM-RFE-GS), support vector machine based on recursive feature elimination and particle swarm optimization (SVM-RFE-PSO), and support vector machine based on recursive feature elimination and genetic algorithm (SVM-RFE-GA). Then the selected optimal feature subsets are used to train the SVM classifier for cancer classification. We also use random forest feature selection (RFFS), random forest feature selection and grid search (RFFS-GS), and minimal redundancy maximal relevance (mRMR) algorithm as feature selection methods to compare the effects of the SVM-RFE-PO algorithm. The results showed that the feature subset obtained by feature selection using SVM-RFE-PSO algorithm results has a better prediction performance of Area Under Curve (AUC) in the testing data set. This algorithm not only is time-saving, but also is capable of extracting more representative and useful genes.

Indexed as

AlgorithmsGene Expression ProfilingSupport Vector MachineArea Under CurveGene ExpressionHumans

Identifiers

PMID30228989
PMCPMC6136508

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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.