Evidence map›Paper›PMID 42598360›Full record

ArticleBioinformatics advances2026

MLHeatmap: an interactive application for transcriptomic marker-panel discovery.

Eun Young Lee, Jihye Park, Seoyeon Youn, Kyungho Choi, Sungryul Yu, Keunsoo Kang

Abstract read
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Article in Bioinformatics advances, 2026. 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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1 · What the graph read from it

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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.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Eun Young LeeDepartment of Biomedical Sciences, College of Bio-Convergence, Dankook University, Cheonan 31116, Republic of Korea.
Jihye ParkDepartment of Biomedical Sciences, College of Bio-Convergence, Dankook University, Cheonan 31116, Republic of Korea.
Seoyeon YounDepartment of Biomedical Sciences, College of Bio-Convergence, Dankook University, Cheonan 31116, Republic of Korea.
Kyungho ChoiGraduate School of Public Health, Seoul National University, Seoul 08826, Republic of Korea.
Sungryul YuDepartment of Clinical Laboratory Science, Semyung University, Jecheon 27136, Republic of Korea.
Keunsoo KangDepartment of Biomedical Sciences, College of Bio-Convergence, Dankook University, Cheonan 31116, Republic of Korea.ORCID https://orcid.org/0000-0003-0611-9320

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: Transcriptomic biomarker studies often require separate tools for normalization, classification, feature ranking, and visualization. MLHeatmap was developed to integrate these steps into a cross-platform, browser-based workflow and to support compact marker-panel discovery directly from count matrices. Results: MLHeatmap accepts a count matrix and sample-group labels and performs gene mapping, normalization, multiclass classification with nested cross-validation, feature attribution, differential expression analysis, and interactive heatmap visualization, with support for multiple classifiers and panel-selection methods in the same workflow. As a case study, we applied MLHeatmap to colorectal cancer consensus molecular subtype (CMS) classification using 511 primary tumors from The Cancer Genome Atlas (TCGA) with published Colorectal Cancer Subtyping Consortium (CRCSC) labels. Random Forest with forward selection achieved 89.8% out-of-fold accuracy and a macro-averaged area under the receiver operating characteristic curve (macro AUC) of 0.973, yielding a 13-gene compact panel with a held-out AUC of 0.960. External validation of the compact panel gave 74.8% accuracy and a macro AUC of 0.917 in GSE39582, an independent Affymetrix GPL570 microarray cohort evaluated in 500 tumors with confident CMScaller-derived CMS assignments, and 69.18% accuracy and a macro AUC of 0.909 in CMCBSN, an independent Korean RNA-seq cohort with 159 confidently labeled tumors. Across the five classifiers and four panel-selection methods evaluated, compact-panel AUCs ranged from 0.895 to 0.970, with tree-ensemble classifiers reaching the highest values. Availability and implementation: MLHeatmap is freely available at https://github.com/kangk1204/MLHeatmap and can be installed and run locally on Windows 11, macOS, and Ubuntu.

Identifiers

PMID42598360
PMCPMC13472729

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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.