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Shared Genomic Segment Analysis: The Power to Find Rare Disease Variants
Shared genomic segment (SGS) analysis is a method that uses dense SNP genotyping in high-risk pedigrees to identify regions of sharing between cases. Here, we illustrate the power of SGS to identify dominant rare risk variants. Using simulated pedigrees, we consider 12 disease models based on diseas...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3879794/ https://ncbi.nlm.nih.gov/pubmed/22989048 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-1809.2012.00728.x |
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