Comparing low-pass sequencing and genotyping for trait mapping in pharmacogenetics

BACKGROUND: Low pass sequencing has been proposed as a cost-effective alternative to genotyping arrays to identify genetic variants that influence multifactorial traits in humans. For common diseases this typically has required both large sample sizes and comprehensive variant discovery. Genotyping...

Descripción completa

Detalles Bibliográficos
Autores principales: Wasik, Kaja, Berisa, Tomaz, Pickrell, Joseph K., Li, Jeremiah H., Fraser, Dana J., King, Karen, Cox, Charles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7981957/
https://www.ncbi.nlm.nih.gov/pubmed/33743587
http://dx.doi.org/10.1186/s12864-021-07508-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7981957/
https://www.ncbi.nlm.nih.gov/pubmed/33743587
http://dx.doi.org/10.1186/s12864-021-07508-2

Ejemplares similares