Cargando…
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...
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: | |
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 |
Ejemplares similares
-
A flexibly shaped spatial scan statistic for detecting clusters
por: Tango, Toshiro, et al.
Publicado: (2005) -
A flexibly shaped space-time scan statistic for disease outbreak detection and monitoring
por: Takahashi, Kunihiko, et al.
Publicado: (2008) -
Detecting multiple spatial disease clusters: information criterion and scan statistic approach
por: Takahashi, Kunihiko, et al.
Publicado: (2020) -
cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing data
por: Samarakoon, Pubudu Saneth, et al.
Publicado: (2016) -
Statistical Methods for Disease Clustering
por: Tango, Toshiro
Publicado: (2010)