A scan statistic to extract causal gene clusters from case-control genome-wide rare CNV data

BACKGROUND: Several statistical tests have been developed for analyzing genome-wide association data by incorporating gene pathway information in terms of gene sets. Using these methods, hundreds of gene sets are typically tested, and the tested gene sets often overlap. This overlapping greatly incr...

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Detalles Bibliográficos
Autores principales: Nishiyama, Takeshi, Takahashi, Kunihiko, Tango, Toshiro, Pinto, Dalila, Scherer, Stephen W, Takami, Satoshi, Kishino, Hirohisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3130692/
https://www.ncbi.nlm.nih.gov/pubmed/21612662
http://dx.doi.org/10.1186/1471-2105-12-205

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3130692/
https://www.ncbi.nlm.nih.gov/pubmed/21612662
http://dx.doi.org/10.1186/1471-2105-12-205

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