Author
Listed:
- Nicasia Beebe-Wang
(Paul G. Allen School of Computer Science and Engineering, University of Washington)
- Safiye Celik
(Recursion Pharmaceuticals)
- Ethan Weinberger
(Paul G. Allen School of Computer Science and Engineering, University of Washington)
- Pascal Sturmfels
(Paul G. Allen School of Computer Science and Engineering, University of Washington)
- Philip L. Jager
(Department of Neurology, Center for Translational and Computational Neuroimmunology, Columbia University Medical Center)
- Sara Mostafavi
(Paul G. Allen School of Computer Science and Engineering, University of Washington
University of British Columbia)
- Su-In Lee
(Paul G. Allen School of Computer Science and Engineering, University of Washington)
Abstract
Deep neural networks (DNNs) capture complex relationships among variables, however, because they require copious samples, their potential has yet to be fully tapped for understanding relationships between gene expression and human phenotypes. Here we introduce an analysis framework, namely MD-AD (Multi-task Deep learning for Alzheimer’s Disease neuropathology), which leverages an unexpected synergy between DNNs and multi-cohort settings. In these settings, true joint analysis can be stymied using conventional statistical methods, which require “harmonized” phenotypes and tend to capture cohort-level variations, obscuring subtler true disease signals. Instead, MD-AD incorporates related phenotypes sparsely measured across cohorts, and learns interactions between genes and phenotypes not discovered using linear models, identifying subtler signals than cohort-level variations which can be uniquely recapitulated in animal models and across tissues. We show that MD-AD exploits sex-specific relationships between microglial immune response and neuropathology, providing a nuanced context for the association between inflammatory genes and Alzheimer’s Disease.
Suggested Citation
Nicasia Beebe-Wang & Safiye Celik & Ethan Weinberger & Pascal Sturmfels & Philip L. Jager & Sara Mostafavi & Su-In Lee, 2021.
"Unified AI framework to uncover deep interrelationships between gene expression and Alzheimer’s disease neuropathologies,"
Nature Communications, Nature, vol. 12(1), pages 1-17, December.
Handle:
RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-25680-7
DOI: 10.1038/s41467-021-25680-7
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-25680-7. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.