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Genotype Imputation Reference Panel Selection Using Maximal Phylogenetic Diversity
The recent dramatic cost reduction of next-generation sequencing technology enables investigators to assess most variants in the human genome to identify risk variants for complex diseases. However, sequencing large samples remains very expensive. For a study sample with existing genotype data, such...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Genetics Society of America
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3781962/ https://www.ncbi.nlm.nih.gov/pubmed/23934887 http://dx.doi.org/10.1534/genetics.113.154591 |