An approch for interpreting disease-associated human variants using single-cell epigenomics
Project description
An approach to interpreting disease-associated human variants using single-cell epigenomics
What can sv_var do?
Identify risk genes, gene sets, and cells related to different stages and diseases.
Infer cell types involved in complex traits and diseases using single-cell epigenomes AND does not rely on any other annotations and other Omics data.
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