Skip to Main Content

Paper Details

Single-cell multiome of the human retina and deep learning nominate causal variants in complex eye diseases.
Cell Genom
21
2022
HiChIP enhancer connectome, SNPs, age-related macular degeneration, chromatin, complex eye diseases, diabetic retinopathy, eQTL, expression quantitative trait loci, eye disease, eye disorders, genetic variants, glaucoma, human, macular telangiectasia, myopia, noncoding SNPs, novel target genes, ocular, single-nucleotide polymorphisms, vision disorders
Author NameAffiliation
Anshul KundajeStanford University
Anshul KundajeStanford University School of Medicine
Anshul KundajeStanford University
Anshul KundajeStanford University School of Medicine
Howard Y ChangCenter for Personal Dynamic Regulomes, Stanford University
Howard Y ChangHoward Hughes Medical Institute, Stanford University
Howard Y Chang
  • 1 - 7

Datasets

Release 1.2