Evidence map›Paper›PMID 38512459›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2024

Identification of important gene signatures in schizophrenia through feature fusion and genetic algorithm.

Zhixiong Chen, Ruiquan Ge, Changmiao Wang, Ahmed Elazab, Xianjun Fu, Wenwen Min, Feiwei Qin, Gangyong Jia, Xiaopeng Fan

Abstract read
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In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 46% of its field
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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 4 institutions in 1 country.

Zhixiong ChenHangzhou Dianzi University, Hangzhou, China.
Ruiquan GeHangzhou Dianzi University, Hangzhou, China. gespring@hdu.edu.cn.
Changmiao WangShenzhen Research Institute of Big Data, Shenzhen, China.
Ahmed ElazabComputer Science Department, Misr Higher Institute for Commerce and Computers, Mansoura, Egypt.
Xianjun FuSchool of Artificial Intelligence, Zhejiang College of Security Technology, Wenzhou, China.
Wenwen MinSchool of Information Science and Engineering, Yunnan University, Kunming, China.
Feiwei QinHangzhou Dianzi University, Hangzhou, China.
Gangyong JiaHangzhou Dianzi University, Hangzhou, China.
Xiaopeng FanHangzhou Institute of Advanced Technology, Hangzhou, China.
Hangzhou Dianzi University · CNHangzhou Institute of Applied Acoustics · CNShenzhen Research Institute of Big Data · CNYunnan University · CN

Funding

GuangDong Basic and Applied Basic Research Foundation 2022A1515110570National Natural Science Foundations of China U20A20386Science and Technology Program of Zhejiang Province 2022C01016Science and Technology Program of Zhejiang Province 2022C03043Zhejiang Provincial Natural Science Foundation of China LY21F020017
6 · The paper itself

Abstract

Schizophrenia is a debilitating psychiatric disorder that can significantly affect a patient's quality of life and lead to permanent brain damage. Although medical research has identified certain genetic risk factors, the specific pathogenesis of the disorder remains unclear. Despite the prevalence of research employing magnetic resonance imaging, few studies have focused on the gene level and gene expression profile involving a large number of screened genes. However, the high dimensionality of genetic data presents a great challenge to accurately modeling the data. To tackle the current challenges, this study presents a novel feature selection strategy that utilizes heuristic feature fusion and a multi-objective optimization genetic algorithm. The goal is to improve classification performance and identify the key gene subset for schizophrenia diagnostics. Traditional gene screening techniques are inadequate for accurately determining the precise number of key genes associated with schizophrenia. Our innovative approach integrates a filter-based feature selection method to reduce data dimensionality and a multi-objective optimization genetic algorithm for improved classification tasks. By combining the filtering and wrapper methods, our strategy leverages their respective strengths in a deliberate manner, leading to superior classification accuracy and a more efficient selection of relevant genes. This approach has demonstrated significant improvements in classification results across 11 out of 14 relevant datasets. The performance on the remaining three datasets is comparable to the existing methods. Furthermore, visual and enrichment analyses have confirmed the practicality of our proposed method as a promising tool for the early detection of schizophrenia.

Indexed as

AlgorithmsSchizophreniaComputational BiologyGene Expression ProfilingGenetic Predisposition to DiseaseHumansTranscriptome

Identifiers

PMID38512459
OpenAlexW4393055921

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.