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Single-cell multiome of the human retina and deep learning nominate causal variants in complex eye diseases
Genome-wide association studies (GWASs) of eye disorders have identified hundreds of genetic variants associated with ocular disease. However, the vast majority of these variants are noncoding, making it challenging to interpret their function. Here we present a joint single-cell atlas of gene expre...
| Autores principales: | , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Elsevier
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9584034/ https://www.ncbi.nlm.nih.gov/pubmed/36277849 http://dx.doi.org/10.1016/j.xgen.2022.100164 |