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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...
Gorde:
| Argitaratua izan da: | J Pers Med |
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| Egile Nagusiak: | , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
MDPI
2021
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7825650/ https://ncbi.nlm.nih.gov/pubmed/33430289 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jpm11010033 |
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