Comparison of scoring methods for the detection of causal genes with or without rare variants

Rare causal variants are believed to significantly contribute to the genetic basis of common diseases or quantitative traits. Appropriate statistical methods are required to discover the highest possible number of disease-relevant variants in a genome-wide screening study. The publicly available Gen...

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Detalles Bibliográficos
Autores principales: Scholz, Markus, Kirsten, Holger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287886/
https://www.ncbi.nlm.nih.gov/pubmed/22373454
http://dx.doi.org/10.1186/1753-6561-5-S9-S49

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287886/
https://www.ncbi.nlm.nih.gov/pubmed/22373454
http://dx.doi.org/10.1186/1753-6561-5-S9-S49

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