Linking regulatory variants to target genes by integrating single-cell multiome methods and genomic distance
Year: 2025
Type: article
Source: Nature Genetics
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: green
Awards: G1007166040, G1403589279, G1700559947, Leveraging functional data to predict disease risk in multi-ethnic populations, G6568865999, G7165297371, G7496421227, G835666399, G8787444564, G9000131021, G9000286330, Cancer Center Support Grant, Statistical methods to localize disease heritability and identify biological mechanisms, Decoding disease-critical genomic architecture using multimodal single-cell omics data, New approaches for leveraging single-cell data to identify disease-critical genes and gene sets, Functional and population genetic architectures of complex disease, Integrating case-control transcriptomic and genetic data in admixed individuals to identify disease genes for schizophrenia and bipolar disorder, Integrative modelling of single-cell data to elucidate the genetic architecture of complex disease, Predicting the impact of genetic variants, genes and pathways on human Disease, Integrative modelling of single-cell data to elucidate the genetic architecture of complex disease
OpenAlex ID: W4411246217
