ArticlebioRxiv : the preprint server for biology2026
MetaPaCS: A Novel Meta-Learning Framework for Pancreatic Cancer Subtype Identification.
Article in bioRxiv : the preprint server for biology, 2026. 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
5 authors.
Funding
Abstract
As the third leading cause of cancer related deaths in the United States, pancreatic cancer (PaC) is a highly heterogenous malignancy that can be divided into a multitude of potential subtypes, with the main 4 consisting of aberrantly differentiated endocrine exocrine (ADEX), immunogenic, progenitor, and squamous. Each PaC subtype is characterized by unique molecular pathways and therapeutic characteristics. Identifying PaC molecular subtypes is essential for downstream patient risk stratification and tailored treatment design. Conventional wet-lab approaches for PaC subtyping like microdissection, histopathological studies or molecular profiling are often laborious, costly, and time-consuming. To address these concerns, we present MetaPaCS, a novel meta-learning framework to accurately identify PaC subtypes based on transcriptomics data only. Specifically, after preprocessing, the transcriptome-based feature vectors were classified by 10 base machine learning (ML) classifiers, whose prediction outputs were then combined with the initial preprocessed feature vectors to constitute a new set of ensemble feature vectors for a meta-learning model. Our meta-learning model could learn and leverage the diversity of different base classifiers to boost the prediction performance beyond any single ML model. Results based on 100 times ten-fold cross validation tests on benchmarking datasets demonstrated that MetaPaCS performed significantly better than existing state-of-the-art methods for PaC subtyping. In addition, our meta-learning model remarkably outperformed each individual base classifier, demonstrating that MetaPaCS could combine diverse results from multiple base classifiers to boost the ensemble performance. We believe that MetaPaCS is a promising tool for characterizing PaC subtypes and will have positive impacts on downstream risk stratification and personalized treatment design for PaC patients.
Indexed as
Identifiers
What OpenQuestion 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 OpenQuestion graph.