Does replication groups scoring reduce false positive rate in SNP interaction discovery?

BACKGROUND: Computational methods that infer single nucleotide polymorphism (SNP) interactions from phenotype data may uncover new biological mechanisms in non-Mendelian diseases. However, practical aspects of such analysis face many problems. Present experimental studies typically use SNP arrays wi...

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Detalles Bibliográficos
Autores principales: Toplak, Marko, Curk, Tomaz, Demsar, Janez, Zupan, Blaz
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2823693/
https://www.ncbi.nlm.nih.gov/pubmed/20092660
http://dx.doi.org/10.1186/1471-2164-11-58

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2823693/
https://www.ncbi.nlm.nih.gov/pubmed/20092660
http://dx.doi.org/10.1186/1471-2164-11-58

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