Novel tree-based method to generate markers from rare variant data

Existing methods for analyzing rare variant data focus on collapsing a group of rare variants into a single common variant; collapsing is based on an intuitive function of the rare variant genotype information, such as an indicator function or a weighted sum. It is more natural, however, to take int...

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Detalles Bibliográficos
Autores principales: Jiang, Yuan, Brennan, Jennifer S, Calixte, Rose, He, Yunxiao, Nyirabahizi, Epiphanie, Zhang, Heping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287825/
https://www.ncbi.nlm.nih.gov/pubmed/22373418
http://dx.doi.org/10.1186/1753-6561-5-S9-S102

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287825/
https://www.ncbi.nlm.nih.gov/pubmed/22373418
http://dx.doi.org/10.1186/1753-6561-5-S9-S102

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