Evidence map›Paper›PMID 35999505›Full record

SynthesisBMC bioinformatics2022

A novel meta-analysis based on data augmentation and elastic data shared lasso regularization for gene expression.

Hai-Hui Huang, Hao Rao, Rui Miao, Yong Liang

Abstract readMeta-Analysis
In one paragraph

Synthesis in BMC bioinformatics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
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  6. Neural networks prediction of the protein-ligand binding affinity with circular fingerprints.Technology and health care : official journal of the European Society for Engineering and Medicine · 2023
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  9. Review
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hai-Hui HuangProvincial Demonstration Software Institute, Shaoguan University, Shaoguan, China.
Hao RaoProvincial Demonstration Software Institute, Shaoguan University, Shaoguan, China.
Rui MiaoFaculty of Information Technology, Macau University of Science and Technology, Macau, China.
Yong LiangThe Peng Cheng Laboratory, Shenzhen, China. yliang_research@163.com.

Funding

National Natural Science Foundation of China 62006155National Natural Science Foundation of China 6201101081National Natural Science Foundation of China 62102261Science and Technology Project of Shaoguan City 200811104531028The Science and Technology Development Fund, Macau SAR 0056/2020/AFJThe Science and Technology Development Fund, Macau SAR 0158/2019/A3
6 · The paper itself

Abstract

backgroundGene expression analysis can provide useful information for analyzing complex biological mechanisms. However, many reported findings are unrepeatable due to small sample sizes relative to a large number of genes and the low signal-to-noise ratios of most gene expression datasets.

resultsMeta-analysis of multi-data sets is an efficient method for tackling the above problem. To improve the performance of meta-analysis, we propose a novel meta-analysis framework. It consists of two parts: (1) a novel data augmentation strategy. Various cross-platform normalization methods exist, which can preserve original biological information of gene expression datasets from different angles and add different "perturbations" to the dataset. Using such perturbation, we provide a feasible means for gene expression data augmentation; (2) elastic data shared lasso (DSL-[Formula: see text]). The DSL-[Formula: see text] method spans the continuum between individual models for each dataset and one model for all datasets. It also overcomes the shortcomings of the data shared lasso method when dealing with highly correlated features. Comprehensive simulation experiment results show that the proposed method has high prediction and gene selection performance. We then apply the proposed method to non-small cell lung cancer (NSCLC) blood gene expression data in order to identify key tumor-related genes. The outcomes of our experiment indicate that the method could be used for identifying a set of robust disease-related gene signatures that may be used for NSCLC early diagnosis or prognosis or even targeting.

conclusionWe propose a novel and effective meta-analysis method for biological research, extrapolating and integrating information from multiple gene expression datasets.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAlgorithmsGene ExpressionGene Expression ProfilingGenes, NeoplasmHumansGene expressionIntegrative analysisMeta-analysisRegularizationVariable selection

Identifiers

PMID35999505
PMCPMC9396780

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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.