Evidence map›Paper›PMID 40880285›Full record

ArticleBioinformatics (Oxford, England)2025

PLSKO: a robust knockoff generator to control false discovery rate in omics variable selection.

Guannan Yang, Ellen Menkhorst, Evdokia Dimitriadis, Kim-Anh Lê Cao

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. Cited by 2 papers.

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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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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

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5 · Who and what money

Authors and funding

4 authors.

Guannan YangMelbourne Integrative Genomics, School of Mathematics and Statistics, The University of Melbourne, Parkville, VIC 3010, Australia.ORCID 0000-0002-9134-5551
Ellen MenkhorstDepartment of Obstetrics and Gynaecology, The University of Melbourne, Parkville, VIC 3010, Australia.ORCID 0000-0003-2440-6665
Evdokia DimitriadisDepartment of Obstetrics and Gynaecology, The University of Melbourne, Parkville, VIC 3010, Australia.ORCID 0000-0003-1425-950X
Kim-Anh Lê CaoMelbourne Integrative Genomics, School of Mathematics and Statistics, The University of Melbourne, Parkville, VIC 3010, Australia.ORCID 0000-0003-3923-1116

Funding

China Scholarship Council - University of Melbourne PhD ScholarshipNational Health and Medical Research Council GNT2025648
6 · The paper itself

Abstract

motivationIntegrating the knockoff framework with any variable-selection method delivers stringent false discovery rate (FDR) control without recourse to p-values, offering a powerful alternative for differential expression analysis of high-throughput omics datasets. However, existing knockoff generators rely on restrictive modelling assumptions or coarse approximations that often inflate the FDR when applied to real-world data.

resultsWe introduce Partial Least Squares Knockoff (PLSKO), an efficient, assumption-free generator that remains robust across diverse omics platforms. Our extensive simulations show that PLSKO is the only method to maintain FDR control with sufficient power in complex non-linear settings. Our semi-simulation studies drawn from RNA-seq, proteomics, metabolomics, and microbiome experiments confirm PLSKO generates valid knockoff variables. In pre-eclampsia multi-omics case studies, we combine PLSKO with Aggregation Knockoff to address the randomness of knockoffs and improve power, and demonstrate the method's ability to recover biologically meaningful features. AVAILABILITY AND IMPLEMENTATION: Our proposed algorithm is available on Github (https://github.com/guannan-yang/PLSKO) and Zenodo (https://doi.org/10.5281/zenodo.16879594).

Indexed as

AlgorithmsComputational BiologySoftwareHumansLeast-Squares AnalysisMetabolomicsProteomics

Identifiers

PMID40880285
PMCPMC12449248

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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.