Evidence map›Paper›PMID 38940152›Full record

ArticleBioinformatics (Oxford, England)2024

Probabilistic pathway-based multimodal factor analysis.

Alexander Immer, Stefan G Stark, Francis Jacob, Ximena Bonilla, Tinu Thomas, André Kahles, Sandra Goetze, Emanuela S Milani, Bernd Wollscheid, Tumor Profiler Consortium and 2 more

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. 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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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Alexander ImmerBiomedical Informatics Group, Department of Computer Science, ETH Zurich, 8092 Zurich, Switzerland.
Stefan G StarkBiomedical Informatics Group, Department of Computer Science, ETH Zurich, 8092 Zurich, Switzerland.
Francis JacobOvarian Cancer Research, Department of Biomedicine, University Hospital Basel and University of Basel, 4031 Basel, Switzerland.
Ximena BonillaBiomedical Informatics Group, Department of Computer Science, ETH Zurich, 8092 Zurich, Switzerland.
Tinu ThomasBiomedical Informatics Group, Department of Computer Science, ETH Zurich, 8092 Zurich, Switzerland.
André KahlesBiomedical Informatics Group, Department of Computer Science, ETH Zurich, 8092 Zurich, Switzerland.ORCID 0000-0002-3411-0692
Sandra GoetzeSwiss Institute of Bioinformatics, 1015 Lausanne, Switzerland.
Emanuela S MilaniSwiss Institute of Bioinformatics, 1015 Lausanne, Switzerland.
Bernd WollscheidSwiss Institute of Bioinformatics, 1015 Lausanne, Switzerland.
Tumor Profiler Consortium
Gunnar RätschBiomedical Informatics Group, Department of Computer Science, ETH Zurich, 8092 Zurich, Switzerland.ORCID 0000-0001-5486-8532
Kjong-Van LehmannBiomedical Informatics Group, Department of Computer Science, ETH Zurich, 8092 Zurich, Switzerland.ORCID 0000-0002-1936-298X

Funding

Cancer Center Cologne EssenMax Planck ETH Center for Learning SystemsMinistry of Culture and SciencePersonalized Health and Related TechnologiesState of North Rhine-Westphalia
6 · The paper itself

Abstract

motivationMultimodal profiling strategies promise to produce more informative insights into biomedical cohorts via the integration of the information each modality contributes. To perform this integration, however, the development of novel analytical strategies is needed. Multimodal profiling strategies often come at the expense of lower sample numbers, which can challenge methods to uncover shared signals across a cohort. Thus, factor analysis approaches are commonly used for the analysis of high-dimensional data in molecular biology, however, they typically do not yield representations that are directly interpretable, whereas many research questions often center around the analysis of pathways associated with specific observations.

resultsWe develop PathFA, a novel approach for multimodal factor analysis over the space of pathways. PathFA produces integrative and interpretable views across multimodal profiling technologies, which allow for the derivation of concrete hypotheses. PathFA combines a pathway-learning approach with integrative multimodal capability under a Bayesian procedure that is efficient, hyper-parameter free, and able to automatically infer observation noise from the data. We demonstrate strong performance on small sample sizes within our simulation framework and on matched proteomics and transcriptomics profiles from real tumor samples taken from the Swiss Tumor Profiler consortium. On a subcohort of melanoma patients, PathFA recovers pathway activity that has been independently associated with poor outcome. We further demonstrate the ability of this approach to identify pathways associated with the presence of specific cell-types as well as tumor heterogeneity. Our results show that we capture known biology, making it well suited for analyzing multimodal sample cohorts. AVAILABILITY AND IMPLEMENTATION: The tool is implemented in python and available at https://github.com/ratschlab/path-fa.

Indexed as

Bayes TheoremAlgorithmsComputational BiologyFactor Analysis, StatisticalGene Expression ProfilingHumansMelanomaProteomics

Identifiers

PMID38940152
PMCPMC11256960

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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.