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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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| Veröffentlicht in: | Curr Protoc Hum Genet |
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| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2019
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| Schlagworte: | |
| Online Zugang: | 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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