Abstract
Human biology is rooted in highly specialized cell types programmed by a common genome, 98% of which is outside of genes. Genetic variation in the enormous noncoding space is linked to the majority of disease risk. To address the problem of linking these variants to expression changes in primary human cells, we introduce ExPectoSC, an atlas of modular deep-learning-based models for predicting cell-type-specific gene expression directly from sequence. We provide models for 105 primary human cell types covering 7 organ systems, demonstrate their accuracy, and then apply them to prioritize relevant cell types for complex human diseases. The resulting atlas of sequence-based gene expression and variant effects is publicly available in a user-friendly interface and readily extensible to any primary cell types. We demonstrate the accuracy of our approach through systematic evaluations and apply the models to prioritize ClinVar clinical variants of uncertain significance, verifying our top predictions experimentally.
Original language | English (US) |
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Article number | 100580 |
Journal | Cell Reports Methods |
Volume | 3 |
Issue number | 9 |
DOIs | |
State | Published - Sep 25 2023 |
All Science Journal Classification (ASJC) codes
- Genetics
- Biochemistry, Genetics and Molecular Biology (miscellaneous)
- Biochemistry
- Radiology Nuclear Medicine and imaging
- Biotechnology
- Computer Science Applications
Keywords
- CP: Systems biology
- deep learning
- functional genomics
- gene expression prediction
- human disease
- variant effects