טוען...
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...
שמור ב:
| הוצא לאור ב: | Curr Protoc Hum Genet |
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| Main Authors: | , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2019
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| נושאים: | |
| גישה מקוונת: | 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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