Cargando…
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...
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 |
Ejemplares similares
-
Sex Differences in the Association between Risk of Anterior Cruciate Ligament Rupture and COL5A1 Polymorphisms in Elite Footballers
por: Rodas, Gil, et al.
Publicado: (2022) -
A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data
por: González, Juan R, et al.
Publicado: (2011) -
SNP Arrays
por: Louhelainen, Jari
Publicado: (2016) -
Following the footprints of polymorphic inversions on SNP data: from detection to association tests
por: Cáceres, Alejandro, et al.
Publicado: (2015) -
Genome-Wide SNP Detection, Validation, and Development of an 8K SNP Array for Apple
por: Chagné, David, et al.
Publicado: (2012)