MCKAT: a multi-dimensional copy number variant kernel association test

BACKGROUND: Copy number variants (CNVs) are the gain or loss of DNA segments in the genome. Studies have shown that CNVs are linked to various disorders, including autism, intellectual disability, and schizophrenia. Consequently, the interest in studying a possible association of CNVs to specific di...

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Detalles Bibliográficos
Autores principales: Maus Esfahani, Nastaran, Catchpoole, Daniel, Khan, Javed, Kennedy, Paul J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666084/
https://www.ncbi.nlm.nih.gov/pubmed/34895138
http://dx.doi.org/10.1186/s12859-021-04494-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8666084/
https://www.ncbi.nlm.nih.gov/pubmed/34895138
http://dx.doi.org/10.1186/s12859-021-04494-w

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