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Fully exploiting SNP arrays: a systematic review on the tools to extract underlying genomic structure

Single nucleotide polymorphisms (SNPs) are the most abundant type of genomic variation and the most accessible to genotype in large cohorts. However, they individually explain a small proportion of phenotypic differences between individuals. Ancestry, collective SNP effects, structural variants, som...

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Detalles Bibliográficos
Autores principales: Balagué-Dobón, Laura, Cáceres, Alejandro, González, Juan R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8921734/
https://www.ncbi.nlm.nih.gov/pubmed/35211719
http://dx.doi.org/10.1093/bib/bbac043