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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Detalhes bibliográficos
Publicado no:BMC Genet
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7507649/
https://ncbi.nlm.nih.gov/pubmed/32957965
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12863-020-00917-4
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