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Methods for the analysis and interpretation for rare variants associated with complex traits
With the advent of Next Generation Sequencing (NGS) technologies, whole genome and whole exome DNA sequencing has become affordable for routine genetic studies. Coupled with improved genotyping arrays and genotype imputation methodologies, it is increasingly feasible to get rare genetic variant info...
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| Publicado no: | Curr Protoc Hum Genet |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6455968/ https://ncbi.nlm.nih.gov/pubmed/30849219 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/cphg.83 |
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