Evidence map›Paper›PMID 40662804›Full record

ArticleBioinformatics (Oxford, England)2025

GRACKLE: an interpretable matrix factorization approach for biomedical representation learning.

Lucas A Gillenwater, Lawrence E Hunter, James C Costello

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Lucas A GillenwaterDepartment of Pharmacology, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, United States.
Lawrence E HunterDepartment of Pediatrics, University of Chicago, Chicago, IL, 60637, United States.
James C CostelloDepartment of Pharmacology, University of Colorado Anschutz Medical Campus, Aurora, CO, 80045, United States.ORCID 0000-0003-3158-9682

Funding

PREDOCTORAL TRAINING PROGRAM IN PHARMACOLOGYT32GM007635 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI DELL'ACQUA, MARK L · 1985 to 2023
$6.1M
Novel computational strategies to deconvolute co-occurring conditions in Down syndromeR01HD109765 · NICHD · UNIVERSITY OF COLORADO DENVER · PI James Christopher Costello, Casey S Greene · 2022 to 2026
$4.1M
Linda Crnic Institute GM007635Linda Crnic Institute HD109765NICHD NIH HHS R01 HD109765NIGMS NIH HHS T32 GM007635
6 · The paper itself

Abstract

motivationDisruption in normal gene expression can contribute to the development of diseases and chronic conditions. However, identifying disease-specific gene signatures can be challenging due to the presence of multiple co-occurring conditions and limited sample sizes. Unsupervised representation learning methods, such as matrix decomposition and deep learning, simplify high-dimensional data into understandable patterns, but often do not provide clear biological explanations. Incorporating prior biological knowledge directly can enhance understanding and address small sample sizes. Nevertheless, current models do not jointly consider prior knowledge of molecular interactions and sample labels.

resultsWe present GRACKLE, a novel nonnegative matrix factorization approach that applies Graph Regularization Across Contextual KnowLedgE. GRACKLE integrates sample similarity and gene similarity matrices based on sample metadata and molecular relationships, respectively. Simulation studies show GRACKLE outperformed other NMF algorithms, especially with increased background noise. GRACKLE effectively stratified breast tumor samples and identified condition-enriched subgroups in individuals with Down syndrome. The model's latent representations aligned with known biological patterns, such as autoimmune conditions and sleep apnea in Down syndrome. GRACKLE's flexibility allows application to various data modalities, offering a robust solution for identifying context-specific molecular mechanisms in biomedical research. AVAILABILITY AND IMPLEMENTATION: GRACKLE is available at: https://github.com/lagillenwater/GRACKLE.

Indexed as

Computational BiologySoftwareAlgorithmsBreast NeoplasmsGene Expression ProfilingHumans

Identifiers

PMID40662804
PMCPMC12261436

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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.