An individualized Bayesian method for estimating genomic variants of hypertension

BACKGROUND: Genomic variants of the disease are often discovered nowadays through population-based genome-wide association studies (GWAS). Identifying genomic variations potentially underlying a phenotype, such as hypertension, in an individual is important for designing personalized treatment; howe...

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Detalles Bibliográficos
Autores principales: Rahman, Md Asad, Cai, Chunhui, Bo, Na, McNamara, Dennis M., Ding, Ying, Cooper, Gregory F., Lu, Xinghua, Liu, Jinling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10631115/
https://www.ncbi.nlm.nih.gov/pubmed/37936055
http://dx.doi.org/10.1186/s12864-023-09757-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10631115/
https://www.ncbi.nlm.nih.gov/pubmed/37936055
http://dx.doi.org/10.1186/s12864-023-09757-9

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