Cargando…
Independent test assessment using the extreme value distribution theory
The new generation of whole genome sequencing platforms offers great possibilities and challenges for dissecting the genetic basis of complex traits. With a very high number of sequence variants, a naïve multiple hypothesis threshold correction hinders the identification of reliable associations by...
Autores principales: | Almeida, Marcio, Blondell, Lucy, Peralta, Juan M., Kent, Jack W., Jun, Goo, Teslovich, Tanya M., Fuchsberger, Christian, Wood, Andrew R., Manning, Alisa K., Frayling, Timothy M., Cingolani, Pablo E., Sladek, Robert, Dyer, Thomas D., Abecasis, Goncalo, Duggirala, Ravindranath, Blangero, John |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5133519/ https://www.ncbi.nlm.nih.gov/pubmed/27980644 http://dx.doi.org/10.1186/s12919-016-0038-5 |
Ejemplares similares
-
Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees
por: Almasy, Laura, et al.
Publicado: (2014) -
Pedigree-based random effect tests to screen gene pathways
por: Almeida, Marcio, et al.
Publicado: (2014) -
Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19
por: Blangero, John, et al.
Publicado: (2016) -
Do rare variant genotypes predict common variant genotypes?
por: Kent, Jack W, et al.
Publicado: (2011) -
Evaluation of estimated genetic values and their application to genome-wide investigation of systolic blood pressure
por: Quillen, Ellen E, et al.
Publicado: (2014)