Evidence map›Paper›PMID 40859122›Full record

ArticleBMC bioinformatics2025

fuseMLR: an R package for integrative prediction modeling of multi-omics data.

Césaire J K Fouodo, Marina Bleskina, Silke Szymczak

Abstract read
In one paragraph

Article in BMC bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

Who cites it

2 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Césaire J K FouodoInstitut für Medizinische Biometrie und Statistik, Universität zu Lübeck and Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Ratzeburger Allee, 23562, Lübeck, Schleswig-Holstein, Germany. cesaire.kuetefouodo@uni-luebeck.de.
Marina Bleskina *Institut für Medizinische Biometrie und Statistik, Universität zu Lübeck and Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Ratzeburger Allee, 23562, Lübeck, Schleswig-Holstein, Germany.
Silke SzymczakInstitut für Medizinische Biometrie und Statistik, Universität zu Lübeck and Universitätsklinikum Schleswig-Holstein, Campus Lübeck, Ratzeburger Allee, 23562, Lübeck, Schleswig-Holstein, Germany. silke.szymczak@uni-luebeck.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent technological advances have enabled the simultaneous collection of multi-omics data, i.e., different types or modalities of molecular data. Integrative predictive modeling of such data is particularly challenging. Ideally, data from the different modalities are measured in the same individuals, allowing for early or intermediate integrative techniques. However, they are often not applicable when patient data only partially overlap, which requires either reducing the datasets or imputing missing values. Additionally, the diversity of data modalities may necessitate specific statistical methods rather than applying the same method across all modalities. Late integration modeling approaches analyze each data modality separately to obtain modality-specific predictions. These predictions are then aggregated into a meta-model by training a machine learning (ML) model, or by computing the weighted mean of modality-specific predictions.

resultsWe introduce the R package fuseMLR for late integration prediction modeling. The package is user-friendly, enables variable selection and the application of different ML algorithms for each modality, and automatically performs aggregation once modality-specific training is completed. We illustrate the package’s functionality in a small simulation study and with two publicly available multi-omics datasets from The Cancer Genome Atlas.

conclusionThe package fuseMLR enables predictive modeling with late integration in a systematic, structured, and reproducible way.

Indexed as

Computational BiologyGenomicsMultiomicsSoftwareAlgorithmsHumansMachine LearningPrediction AlgorithmsPredictive Learning ModelsIntegrative predictive modelingMulti-omicsVariable selection

Identifiers

PMID40859122
PMCPMC12382258

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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.