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Combination of Genome-Wide Polymorphisms and Copy Number Variations of Pharmacogenes in Koreans

For predicting phenotypes and executing precision medicine, combination analysis of single nucleotide variants (SNVs) genotyping with copy number variations (CNVs) is required. The aim of this study was to discover SNVs or common copy CNVs and examine the combined frequencies of SNVs and CNVs in pha...

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Detalles Bibliográficos
Autores principales: Han, Nayoung, Oh, Jung Mi, Kim, In-Wha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7825650/
https://www.ncbi.nlm.nih.gov/pubmed/33430289
http://dx.doi.org/10.3390/jpm11010033