Plate IV.217 · Publications

Network reconstruction for trans acting genetic loci using multi-omics data and prior information

Article in Genome Medicine, 7 November 2022.

Open accessResearch area: Spatial, Omics Data

Authors

  1. Johann S. Hawe
  2. Ashis Saha
  3. Melanie Waldenberger
  4. Sonja Kunze
  5. Simone Wahl
  6. Martina Müller-Nurasyid
  7. Holger Prokisch
  8. Harald Grallert
  9. Christian Herder
  10. Annette Peters
  11. Konstantin Strauch
  12. Fabian J. Theis
  13. Christian Gieger
  14. John Chambers
  15. Alexis Battle
  16. Matthias Heinig

Abstract

Background Molecular measurements of the genome, the transcriptome, and the epigenome, often termed multi-omics data, provide an in-depth view on biological systems and their integration is crucial for gaining insights in complex regulatory processes. These data can be used to explain disease related genetic variants by linking them to intermediate molecular traits (quantitative trait loci, QTL). Molecular networks regulating cellular processes leave footprints in QTL results as so-called trans-QTL hotspots. Reconstructing these networks is a complex endeavor and use of biological prior information can improve network inference. However, previous efforts were limited in the types of priors used or have only been applied to model systems. In this study, we reconstruct the regulatory networks underlying trans-QTL hotspots using human cohort data and data-driven prior information. Methods We devised a new strategy to integrate QTL with human population scale multi-omics data. State-of-the art network inference methods including BDgraph and glasso were applied to these data. Comprehensive prior information to guide network inference was manually curated from large-scale biological databases. The inference approach was extensively benchmarked using simulated data and cross-cohort replication analyses. Best performing methods were subsequently applied to real-world human cohort data. Results Our benchmarks showed that prior-based strategies outperform methods without prior information in simulated data and show better replication across datasets. Application of our approach to human cohort data highlighted two novel regulatory networks related to schizophrenia and lean body mass for which we generated novel functional hypotheses. Conclusions We demonstrate that existing biological knowledge can improve the integrative analysis of networks underlying trans associations and generate novel hypotheses about regulatory mechanisms.

Versions2

  1. PublishedGenome Medicine10.1186/s13073-022-01124-9
  2. PreprintbioRxiv10.1101/2020.05.19.101592

Cite

@article{hawe2022network,
  title = {{Network reconstruction for trans acting genetic loci using multi-omics data and prior information}},
  author = {Hawe, Johann S. and Saha, Ashis and Waldenberger, Melanie and Kunze, Sonja and Wahl, Simone and Müller-Nurasyid, Martina and Prokisch, Holger and Grallert, Harald and Herder, Christian and Peters, Annette and Strauch, Konstantin and Theis, Fabian J. and Gieger, Christian and Chambers, John and Battle, Alexis and Heinig, Matthias},
  journal = {Genome Medicine},
  publisher = {Springer Science and Business Media LLC},
  year = {2022},
  month = nov,
  doi = {10.1186/s13073-022-01124-9},
  url = {https://doi.org/10.1186/s13073-022-01124-9},
  pmid = {36344995},
  pmcid = {PMC9641770}
}
.bib file