Literature DB >> 17685457

Missing phenotype data imputation in pedigree data analysis.

Brooke L Fridley1, Mariza de Andrade.   

Abstract

Mapping complex traits or phenotypes with small genetic effects, whose phenotypes may be modulated by temporal trends in families are challenging. Detailed and accurate data must be available on families, whether or not the data were collected over time. Missing data complicate matters in pedigree analysis, especially in the case of a longitudinal pedigree analysis. Because most analytical methods developed for the analysis of longitudinal pedigree data require no missing data, the researcher is left with the option of dropping those cases (individuals) with missing data from the analysis or imputing values for the missing data. We present the use of data augmentation within Bayesian polygenic and longitudinal polygenic models to produce k complete datasets. The data augmentation, or imputation step of the Markov chain Monte Carlo, takes into account the observed familial information and the observed subject information available at other time points. These k complete datasets can then be used to fit single time point or longitudinal pedigree models. By producing a set of k complete datasets and thus k sets of parameter estimates, the total variance associated with an estimate can be partitioned into a within-imputation and a between-imputation component. The method is illustrated using the Genetic Analysis Workshop simulated data.

Entities:  

Mesh:

Year:  2008        PMID: 17685457     DOI: 10.1002/gepi.20261

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  3 in total

1.  Localizing putative markers in genetic association studies by incorporating linkage disequilibrium into bayesian hierarchical models.

Authors:  Brooke L Fridley; Gregory D Jenkins
Journal:  Hum Hered       Date:  2010-06-10       Impact factor: 0.444

2.  Multiple imputation of missing phenotype data for QTL mapping.

Authors:  Jennifer F Bobb; Daniel O Scharfstein; Michael J Daniels; Francis S Collins; Samir Kelada
Journal:  Stat Appl Genet Mol Biol       Date:  2011

3.  Candidate gene analysis using imputed genotypes: cell cycle single-nucleotide polymorphisms and ovarian cancer risk.

Authors:  Ellen L Goode; Brooke L Fridley; Robert A Vierkant; Julie M Cunningham; Catherine M Phelan; Stephanie Anderson; David N Rider; Kristin L White; V Shane Pankratz; Honglin Song; Estrid Hogdall; Susanne K Kjaer; Alice S Whittemore; Richard DiCioccio; Susan J Ramus; Simon A Gayther; Joellen M Schildkraut; Paul P D Pharaoh; Thomas A Sellers
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2009-03-03       Impact factor: 4.254

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.