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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Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Nishiyama, Takeshi, Takahashi, Kunihiko, Tango, Toshiro, Pinto, Dalila, Scherer, Stephen W, Takami, Satoshi, Kishino, Hirohisa
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2011
Gaiak:
Methodology Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC3130692/
https://ncbi.nlm.nih.gov/pubmed/21612662
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-12-205
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