Identification of single nucleotide variants in the Moroccan population by whole-genome sequencing

BACKGROUND: Large-scale human sequencing projects have described around a hundred-million single nucleotide variants (SNVs). These studies have predominately involved individuals with European ancestry despite the fact that genetic diversity is expected to be highest in Africa where Homo sapiens evo...

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Detalles Bibliográficos
Autores principales: Crooks, Lucy, Cooper-Knock, Johnathan, Heath, Paul R., Bouhouche, Ahmed, Elfahime, Mostafa, Azzouz, Mimoun, Bakri, Youssef, Adnaoui, Mohammed, Ibrahimi, Azeddine, Amzazi, Saaïd, Tazi-Ahnini, Rachid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507649/
https://www.ncbi.nlm.nih.gov/pubmed/32957965
http://dx.doi.org/10.1186/s12863-020-00917-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507649/
https://www.ncbi.nlm.nih.gov/pubmed/32957965
http://dx.doi.org/10.1186/s12863-020-00917-4

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