CLIN_SKAT: an R package to conduct association analysis using functionally relevant variants

BACKGROUND: Availability of next generation sequencing data, allows low-frequency and rare variants to be studied through strategies other than the commonly used genome-wide association studies (GWAS). Rare variants are important keys towards explaining the heritability for complex diseases that rem...

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Detalles Bibliográficos
Autores principales: Chattopadhyay, Amrita, Shih, Ching-Yu, Hsu, Yu-Chen, Juang, Jyh-Ming Jimmy, Chuang, Eric Y., Lu, Tzu-Pin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9590128/
https://www.ncbi.nlm.nih.gov/pubmed/36274122
http://dx.doi.org/10.1186/s12859-022-04987-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9590128/
https://www.ncbi.nlm.nih.gov/pubmed/36274122
http://dx.doi.org/10.1186/s12859-022-04987-2

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