Evidence map›Paper›PMID 40098088›Full record

ArticleBMC bioinformatics2025

Transfer learning for accelerated failure time model with microarray data.

Yan-Bo Pei, Zheng-Yang Yu, Jun-Shan Shen

Abstract read
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Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Yan-Bo PeiSchool of Statistics, Capital University of Economics and Business, Beijing, China.
Zheng-Yang YuSchool of Statistics, Capital University of Economics and Business, Beijing, China.
Jun-Shan ShenSchool of Statistics, Capital University of Economics and Business, Beijing, China. shenjunshan@cueb.edu.cn.

Funding

Capital University of Economics and Business special fund for basic scientific research and business expenses of Beijing affiliated universities (QNTD202207) QNTD202207
6 · The paper itself

Abstract

backgroundIn microarray prognostic studies, researchers aim to identify genes associated with disease progression. However, due to the rarity of certain diseases and the cost of sample collection, researchers often face the challenge of limited sample size, which may prevent accurate estimation and risk assessment. This challenge necessitates methods that can leverage information from external data (i.e., source cohorts) to improve gene selection and risk assessment based on the current sample (i.e., target cohort).

methodWe propose a transfer learning method for the accelerated failure time (AFT) model to enhance the fit on the target cohort by adaptively borrowing information from the source cohorts. We use a Leave-One-Out cross validation based procedure to evaluate the relative stability of selected genes and overall predictive power.

conclusionIn simulation studies, the transfer learning method for the AFT model can correctly identify a small number of genes, its estimation error is smaller than the estimation error obtained without using the source cohorts. Furthermore, the proposed method demonstrates satisfactory accuracy and robustness in addressing heterogeneity across the cohorts compared to the method that directly combines the target and the source cohorts in the AFT model. We analyze the GSE88770 and GSE25055 data using the proposed method. The selected genes are relatively stable, and the proposed method can make an overall satisfactory risk prediction.

Indexed as

Gene Expression ProfilingMachine LearningOligonucleotide Array Sequence AnalysisAlgorithmsHumansAuxiliary studiesGene expression dataSurvival analysisTransfer learningWeighted least squares

Identifiers

PMID40098088
PMCPMC11917065

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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.