Evidence map›Paper›PMID 30373514›Full record

ArticleBMC bioinformatics2018

Feature selection of gene expression data for Cancer classification using double RBF-kernels.

Shenghui Liu, Chunrui Xu, Yusen Zhang, Jiaguo Liu, Bin Yu, Xiaoping Liu, Matthias Dehmer

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–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

22 citing papers in PubMed.

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  4. ProkDBP: Toward more precise identification of prokaryotic DNA binding proteins.Protein science : a publication of the Protein Society · 2024
    Article
  5. Novel candidate genes for environmental stresses response in Synechocystis sp. PCC 6803 revealed by machine learning algorithms.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2024
    Article
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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

7 authors.

Shenghui LiuSchool of Mathematics and Statistics, Shandong University at Weihai, Weihai, 264209, China.
Chunrui XuSchool of Mathematics and Statistics, Shandong University at Weihai, Weihai, 264209, China.
Yusen ZhangSchool of Mathematics and Statistics, Shandong University at Weihai, Weihai, 264209, China. zhangys@sdu.edu.cn.ORCID http://orcid.org/0000-0003-3842-1153
Jiaguo LiuSchool of Mathematics and Statistics, Shandong University at Weihai, Weihai, 264209, China.
Bin YuCollege of Mathematics and Physics, Qingdao University of Science and Technology, Qingdao, 266061, China.
Xiaoping LiuSchool of Mathematics and Statistics, Shandong University at Weihai, Weihai, 264209, China. xpliu@sdu.edu.cn.
Matthias DehmerInstitute for Intelligent Production, Faculty for Management, University of Applied Sciences Upper Austria, Steyr Campus, Steyr, Austria.

Funding

Austrian Science Funds P26142National Natural Science Foundation of China Nos. 61877064Natural Science Foundation of Shandong Province ZR2015AM017
6 · The paper itself

Abstract

backgroundUsing knowledge-based interpretation to analyze omics data can not only obtain essential information regarding various biological processes, but also reflect the current physiological status of cells and tissue. The major challenge to analyze gene expression data, with a large number of genes and small samples, is to extract disease-related information from a massive amount of redundant data and noise. Gene selection, eliminating redundant and irrelevant genes, has been a key step to address this problem.

resultsThe modified method was tested on four benchmark datasets with either two-class phenotypes or multiclass phenotypes, outperforming previous methods, with relatively higher accuracy, true positive rate, false positive rate and reduced runtime.

conclusionsThis paper proposes an effective feature selection method, combining double RBF-kernels with weighted analysis, to extract feature genes from gene expression data, by exploring its nonlinear mapping ability.

Indexed as

AlgorithmsGene Expression Regulation, NeoplasticComputational BiologyGene Expression ProfilingHumansNeoplasm ProteinsNeoplasmsPhenotypeNeoplasm ProteinsCancer classificationClusteringData miningFeature selectionGene expression

Identifiers

PMID30373514
PMCPMC6206917

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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.