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Protocol for using GRPath to identify putative gene regulation paths in complex human diseases
Unfolding the “black-box” associations between genotype and phenotype is essential for understanding the molecular mechanisms of complex human diseases. Here, we describe the use of GRPath to uncover putative causal paths (pcPaths) from genetic variants to disease phenotypes. GRPath takes multiple o...
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/PMC9664398/ https://www.ncbi.nlm.nih.gov/pubmed/36386883 http://dx.doi.org/10.1016/j.xpro.2022.101831 |