Evidence map›Paper›PMID 42152108›Full record

ArticleGenome medicine2026

DNA methylation biomarkers-based pan-cancer classifier: predictive modeling for cancer classification.

Jan Bińkowski, Tomasz K Wojdacz

Abstract read
In one paragraph

Article in Genome medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Jan BińkowskiIndependent Clinical Epigenetics Laboratory, Pomeranian Medical University in Szczecin, Szczecin, Poland.
Tomasz K WojdaczIndependent Clinical Epigenetics Laboratory, Pomeranian Medical University in Szczecin, Szczecin, Poland. tomasz.wojdacz@pum.edu.pl.

Funding

Narodowe Centrum Nauki 2021/43/B/NZ2/02979
6 · The paper itself

Abstract

backgroundMachine-learning (ML) driven molecular diagnostics based on omics data has a potential to revolutionize personalized medicine. However, implementation of ML into diagnostic protocols is hindered by methodological challenges which often lead to inflated performance assessment of models during development followed by poor performance of these models in implementation phase. Here, we aimed to develop and validate a pan-cancer classification framework based on DNA methylation data, that addresses methodological challenges of omics data powered ML.

methodsWe curated a primary dataset of DNA methylation profiles for 10756 samples, that included 54 healthy and cancer tissue types and validation dataset comprising data for 2306 samples from 28 independent studies. The classification framework was build using custom biomarkers selection strategy based on effect size metric that considers variance and class imbalance. The ML models were trained, tuned and evaluated using nested cross-validation approach. Local outlier factor algorithm was built into the inference pipelines to identify and filter samples displaying technical or biological anomalies. Additionally, for methodological validation of our framework we used methylation profiles for 3905 central nervous system (CNS) tumors.

resultsWe found that relatively simple ML models outperformed complex algorithms such as deep neural network. A logistic regression classifier achieved a balanced accuracy (BACC) of 0.90 to classify 54 cancer and healthy tissue types using methylation levels at 1208 CpG sites. Similarly, our CNS tumor classifier also based on logistic regression algorithm reached a BACC of 0.94 across 59 CNS tumor subtypes. The anomaly filtering improved performance across all categories of samples tested.

conclusionsOur study demonstrates that DNA methylation profiling, when combined with carefully controlled ML practices allows for development of robust solutions that might substantially increase the efficacy of oncological diagnosis. Finally, we deployed our inference pipelines for public access via secure web platform - https://opp.pum.edu.pl/ .

Indexed as

Biomarkers, TumorDNA MethylationNeoplasmsAlgorithmsClassification AlgorithmsHumansMachine LearningPrediction AlgorithmsPredictive Learning ModelsBiomarkers, TumorBiomarkersCancerClassificationDNA methylationMachine-learning

Identifiers

PMID42152108
PMCPMC13185202

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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.