integRATE: a desirability-based data integration framework for the prioritization of candidate genes across heterogeneous omics and its application to preterm birth
Haley R. Eidem, Jacob Lucas SteenwykiD, Jennifer H. WisecaveriD, John A. CapraiD, Patrick AbbotiD, Antonis RokasiD
Abstract
BackgroundThe integration of high-quality, genome-wide analyses offers a robust approach to elucidating genetic factors involved in complex human diseases. Even though several methods exist to integrate heterogeneous omics data, most biologists still manually select candidate genes by examining the intersection of lists of candidates stemming from analyses of different types of omics data that have been generated by imposing hard (strict) thresholds on quantitative variables, such as P-values and fold changes, increasing the chance of missing potentially important candidates.\n\nMethodsTo better facilitate the unbiased integration of heterogeneous omics data collected from diverse platforms and samples, we propose a desirability function framework for identifying candidate genes with strong evidence across data types as targets for follow-up functional analysis. Our approach is targeted towards disease systems with sparse, heterogeneous omics data, so we tested it on one such pathology: spontaneous preterm birth (sPTB).\n\nResultsWe developed the software integRATE, which uses desirability functions to rank genes both within and across studies, identifying well-supported candidate genes according to the cumulative weight of biological evidence rather than based on imposition of hard thresholds of key variables. Integrating 10 sPTB omics studies identified both genes in pathways previously suspected to be involved in sPTB as well as novel genes never before linked to this syndrome. integRATE is available as an R package on GitHub (https://github.com/haleyeidem/integRATE).\n\nConclusionsDesirability-based data integration is a solution most applicable in biological research areas where omics data is especially heterogeneous and sparse, allowing for the prioritization of candidate genes that can be used to inform more targeted downstream functional analyses.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 8
- FWCI
- 0.09
- Field percentile
- 43th percentile
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Multi-omic data integration and analyses for biomarker discovery of spontaneous preterm birth phenotypes
Juhi K. Gupta, Angharad Care, … Bertram Müller‐Myhsok·bioRxiv·Jan 31, 2025
- Rank-based integration identifies convergent disease mechanisms across omics
Zifeng Qiu, Duncan Palmer, … Yang Luo·bioRxiv·Oct 1, 2026
- mixOmics: an R package for ‘omics feature selection and multiple data integration
Florian Rohart, Benoît Gautier, … Kim‐Anh Lê Cao·PLoS Computational BiologyPeer-reviewed·Nov 3, 2017
- PathIntegrate: Multivariate modelling approaches for pathway-based multi-omics data integration
Cecilia Wieder, Juliette Cooke, … Timothy M. D. Ebbels·PLoS Computational BiologyPeer-reviewed·Mar 25, 2024
- GraphOmics: an Interactive Platform to Explore and Integrate Multi-Omics Data
Joe Wandy, Rónán Daly·BMC BioinformaticsPeer-reviewed·Dec 1, 2021
- TiMEG: an integrative approach for partially missing multi-omics data with an application to tuberous sclerosis
Sarmistha Das, Indranil Mukhopadhyay·bioRxiv·Dec 10, 2020