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Detecting associations of rare variants with common diseases: collapsing or haplotyping?
In recent years, a myriad of new statistical methods have been proposed for detecting associations of rare single-nucleotide variants (SNVs) with common diseases. These methods can be generally classified as ‘collapsing’ or ‘haplotyping’ based. The former is the predominant class, composed of most o...
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| Publicado en: | Brief Bioinform |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Oxford University Press
2015
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4570202/ https://ncbi.nlm.nih.gov/pubmed/25596401 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bib/bbu050 |
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