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Low-pass sequencing increases the power of GWAS and decreases measurement error of polygenic risk scores compared to genotyping arrays

Low-pass sequencing (sequencing a genome to an average depth less than 1× coverage) combined with genotype imputation has been proposed as an alternative to genotyping arrays for trait mapping and calculation of polygenic scores. To empirically assess the relative performance of these technologies f...

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Detalles Bibliográficos
Autores principales: Li, Jeremiah H., Mazur, Chase A., Berisa, Tomaz, Pickrell, Joseph K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8015847/
https://www.ncbi.nlm.nih.gov/pubmed/33536225
http://dx.doi.org/10.1101/gr.266486.120

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