Variable Selection via Fused Sparse-Group Lasso Penalized Multi-state Models Incorporating Molecular Data.
기술보고
1/5 보강
In multi-state models based on high-dimensional data, effective modeling strategies are required to determine an optimal, ideally parsimonious model.
APA
Miah K, Goeman JJ, et al. (2025). Variable Selection via Fused Sparse-Group Lasso Penalized Multi-state Models Incorporating Molecular Data.. Biometrical journal. Biometrische Zeitschrift, 67(6), e70087. https://doi.org/10.1002/bimj.70087
MLA
Miah K, et al.. "Variable Selection via Fused Sparse-Group Lasso Penalized Multi-state Models Incorporating Molecular Data.." Biometrical journal. Biometrische Zeitschrift, vol. 67, no. 6, 2025, pp. e70087.
PMID
41146443 ↗
Abstract 한글 요약
In multi-state models based on high-dimensional data, effective modeling strategies are required to determine an optimal, ideally parsimonious model. In particular, linking covariate effects across transitions is needed to conduct joint variable selection. A useful technique to reduce model complexity is to address homogeneous covariate effects for distinct transitions. We integrate this approach to data-driven variable selection by extended regularization methods within multi-state model building. We propose the fused sparse-group lasso (FSGL) penalized Cox-type regression in the framework of multi-state models combining the penalization concepts of pairwise differences of covariate effects along with transition-wise grouping. For optimization, we adapt the alternating direction method of multipliers (ADMM) algorithm to transition-specific hazards regression in the multi-state setting. In a simulation study and application to acute myeloid leukemia (AML) data, we evaluate the algorithm's ability to select a sparse model incorporating relevant transition-specific effects and similar cross-transition effects. We investigate settings in which the combined penalty is beneficial compared to global lasso regularization. Clinical Trial Registration: The AMLSG 09-09 trial is registered with ClinicalTrials.gov (NCT00893399) and has been completed.
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