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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
MDPI
2021
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| 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 |