Evidence map›Paper›PMID 31775613›Full record

ArticleBMC bioinformatics2019

Deep gene selection method to select genes from microarray datasets for cancer classification.

Russul Alanni, Jingyu Hou, Hasseeb Azzawi, Yong Xiang

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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.

Russul AlanniSchool of Information Technology, Deakin University, Geelong, Victoria, Australia. ralanni@deakin.edu.au.ORCID http://orcid.org/0000-0002-6445-0137
Jingyu HouSchool of Information Technology, Deakin University, Geelong, Victoria, Australia.
Hasseeb AzzawiSchool of Information Technology, Deakin University, Geelong, Victoria, Australia.
Yong XiangSchool of Information Technology, Deakin University, Geelong, Victoria, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroarray datasets consist of complex and high-dimensional samples and genes, and generally the number of samples is much smaller than the number of genes. Due to this data imbalance, gene selection is a demanding task for microarray expression data analysis.

resultsThe gene set selected by DGS has shown its superior performances in cancer classification. DGS has a high capability of reducing the number of genes in the original microarray datasets. The experimental comparisons with other representative and state-of-the-art gene selection methods also showed that DGS achieved the best performance in terms of the number of selected genes, classification accuracy, and computational cost.

conclusionsWe provide an efficient gene selection algorithm can select relevant genes which are significantly sensitive to the samples' classes. With the few discriminative genes and less cost time by the proposed algorithm achieved much high prediction accuracy on several public microarray data, which in turn verifies the efficiency and effectiveness of the proposed gene selection method.

Indexed as

Genetic TechniquesAlgorithmsGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMicroarray AnalysisNeoplasmsResearch DesignEvolutionary algorithmsGene expression programmingGene selectionMicroarray

Identifiers

PMID31775613
PMCPMC6880643

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Registered trials

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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.