Evidence map›Paper›PMID 36009599›Full record

ArticleBiomedicines2022

Mutational Slime Mould Algorithm for Gene Selection.

Feng Qiu, Pan Zheng, Ali Asghar Heidari, Guoxi Liang, Huiling Chen, Faten Khalid Karim, Hela Elmannai, Haiping Lin

Abstract read
In one paragraph

Article in Biomedicines, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Advances in Slime Mould Algorithm: A Comprehensive Survey.Biomimetics (Basel, Switzerland) · 2024
    Review
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

8 authors.

Feng QiuDepartment of Computer Science and Artificial Intelligence, Wenzhou University, Wenzhou 325035, China.
Pan ZhengInformation Systems, University of Canterbury, Christchurch 8014, New Zealand.ORCID 0000-0002-6067-626X
Ali Asghar HeidariDepartment of Computer Science and Artificial Intelligence, Wenzhou University, Wenzhou 325035, China.
Guoxi LiangDepartment of Information Technology, Wenzhou Polytechnic, Wenzhou 325035, China.ORCID 0000-0003-4754-6644
Huiling ChenDepartment of Computer Science and Artificial Intelligence, Wenzhou University, Wenzhou 325035, China.ORCID 0000-0002-7714-9693
Faten Khalid KarimDepartment of Computer Sciences, College of Computer and Information Sciences, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia.
Hela ElmannaiDepartment of Information Technology, College of Computer and Information Sciences, Princess Nourah bint Abdulrahman University, P.O. Box 84428, Riyadh 11671, Saudi Arabia.ORCID 0000-0003-2571-1848
Haiping LinDepartment of Information Engineering, Hangzhou Vocational & Technical College, Hangzhou 310018, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A large volume of high-dimensional genetic data has been produced in modern medicine and biology fields. Data-driven decision-making is particularly crucial to clinical practice and relevant procedures. However, high-dimensional data in these fields increase the processing complexity and scale. Identifying representative genes and reducing the data's dimensions is often challenging. The purpose of gene selection is to eliminate irrelevant or redundant features to reduce the computational cost and improve classification accuracy. The wrapper gene selection model is based on a feature set, which can reduce the number of features and improve classification accuracy. This paper proposes a wrapper gene selection method based on the slime mould algorithm (SMA) to solve this problem. SMA is a new algorithm with a lot of application space in the feature selection field. This paper improves the original SMA by combining the Cauchy mutation mechanism with the crossover mutation strategy based on differential evolution (DE). Then, the transfer function converts the continuous optimizer into a binary version to solve the gene selection problem. Firstly, the continuous version of the method, ISMA, is tested on 33 classical continuous optimization problems. Then, the effect of the discrete version, or BISMA, was thoroughly studied by comparing it with other gene selection methods on 14 gene expression datasets. Experimental results show that the continuous version of the algorithm achieves an optimal balance between local exploitation and global search capabilities, and the discrete version of the algorithm has the highest accuracy when selecting the least number of genes.

Indexed as

Cauchy mutationcrossover and mutationgene selectionmedical diagnosisslime mould algorithm

Identifiers

PMID36009599
PMCPMC9406076

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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.