ArticleBioengineering (Basel, Switzerland)2025
A Multi-Task Ensemble Strategy for Gene Selection and Cancer Classification.
Article in Bioengineering (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Gene expression-based tumor classification aims to distinguish tumor types based on gene expression profiles. This task is difficult due to the high dimensionality of gene expression data and limited sample sizes. Most datasets contain tens of thousands of genes but only a small number of samples. As a result, selecting informative genes is necessary to improve classification performance and model interpretability. Many existing gene selection methods fail to produce stable and consistent results, especially when training data are limited. To address this, we propose a multi-task ensemble strategy that combines repeated sampling with joint feature selection and classification. The method generates multiple training subsets and applies multi-task logistic regression with ℓ2,1 group sparsity regularization to select a subset of genes that appears consistently across tasks. This promotes stability and reduces redundancy. The framework supports integration with standard classifiers such as logistic regression and support vector machines. It performs both gene selection and classification in a single process. We evaluate the method on simulated and real gene expression datasets. The results show that it outperforms several baseline methods in classification accuracy and the consistency of selected genes.
Indexed as
Identifiers
What Socratic holds
Registered trials
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.