Harmonization of quality metrics and power calculation in multi-omic studies
Open accessAbstract
Multi-omic studies combine measurements at different molecular levels to build comprehensive models of cellular systems. The success of a multi-omic data analysis strategy depends largely on the adoption of adequate experimental designs, and on the quality of the measurements provided by the different omic platforms. However, the field lacks a comparative description of performance parameters across omic technologies and a formulation for experimental design in multi-omic data scenarios. Here, we propose a set of harmonized Figures of Merit (FoM) as quality descriptors applicable to different omic data types. Employing this information, we formulate the MultiPower method to estimate and assess the optimal sample size in a multi-omics experiment. MultiPower supports different experimental settings, data types and sample sizes, and includes graphical for experimental design decision-making. MultiPower is complemented with MultiML, an algorithm to estimate sample size for machine learning classification problems based on multi-omic data.
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MultiPower modeling has shown that approximately 500 paired omics and imaging samples are required to detect moderate molecular effects with a 5% false discovery rate in integrative analyses.
“For instance, MultiPower modeling has shown that approximately 500 paired omics and imaging samples are required to detect moderate molecular effects with a 5% false discovery rate in integrative analyses407.”
From Artificial intelligence-driven multi-omics approaches in Alzheimer's disease: Progress, challenges, and future directions (2025) · cites this paper as [407]
The Results section reports MultiPower sample-size modeling with an FDR of 0.05 and an initial Cohen’s d of 0.8, but estimates 16 replicates for the STATegra multi-omics example. It also estimates n = 24 for a complete-design glioblastoma multi-omics analysis. Neither example supports approximately 500 paired omics and imaging samples; the reported analyses do not include imaging. (LLM, conf=0.90)
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- Authors
- Tarazona, S., Balzano-Nogueira, L., Gómez-Cabrero, D., Schmidt, A., Imhof, A., Hankemeier, T., Tegnér, J., Westerhuis, J. A., & Conesa, A.
- Affiliations
- Universitat Politècnica de València (ES)
- Universidad Pública de Navarra (UPNA) (ES)
- Ludwig-Maximilians-Universität München (DE)
- Center for Integrated Protein Science Munich (DE)
- North-West University (ZA)
- University of Florida (US)
- Corresponding author
- Conesa, Ana
- ORCID
- Venue
- Nature Communications
- Published
- 2020-06-18
- Volume
- 11
- Issue
- 1
- Pages
- 3092-3092
- ISSN
- 2041-1723 (ISSN-L)
- PMC
- PMC7303201
- OpenAlex
- W3036926163
- Cited by
- 105
- References
- 8
- Citations by year
- 2026: 15 · 2025: 26 · 2024: 22 · 2023: 19 · 2022: 14 · 2021: 7 · 2020: 1
- FWCI
- 3.33
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Nature Communications (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- UvA-DARE (University of Amsterdam) (submittedVersion, cc-by)
- RePEc: Research Papers in Economics (submittedVersion)
- Leiden Repository (Leiden University) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Open access LMU (Ludwid Maxmilian's Universitat Munchen) (submittedVersion, cc-by)
- Leiden Repository (Leiden University) (submittedVersion)
- King Abdullah University of Science and Technology Repository (King Abdullah University of Science and Technology) (submittedVersion, other-oa)
- Boloka Institutional Repository (North-west University) (submittedVersion, cc-by)
- RiuNet (Universitat Politècnica de València) (submittedVersion, cc-by-nc-nd)
- Data Archiving and Networked Services (DANS) (submittedVersion, cc-by)
- Data Archiving and Networked Services (DANS) (submittedVersion, other-oa)
- Funders
- EC | EC Seventh Framework Programm | FP7 Health (306000)
- Ministerio de Economía, Industria y Competitividad, Gobierno de España (BIO2012-40244)
- Deutsche Forschungsgemeinschaft (SFB1064)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bioinformatics and Genomic Networks
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene expression and cancer classification
- Social Sciences › Decision Sciences › Management Science and Operations Research › Optimal Experimental Design Methods
- Keywords
- multi-omics, sample size determination, power analysis, figure of merit, experimental design, machine learning classification
- MeSH terms
- Machine Learning, Algorithms, Quality Control, Computational Biology
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