Volume 5, supplement issue 9, December 2011
Genetic Analysis Workshop 17: Unraveling Human Exome Data
- Issue editors
121 articles in this issue
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Identifying influential regions in extremely rare variants using a fixed-bin approach
Authors (first, second and last of 6)
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Identification of genes and variants associated with quantitative traits using Bayesian factor screening
Authors (first, second and last of 4)
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Genome-wide association analysis of GAW17 data using an empirical Bayes variable selection
Authors (first, second and last of 5)
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Population structure analysis using rare and common functional variants
Authors (first, second and last of 6)
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Pairwise shared genomic segment analysis in high-risk pedigrees: application to Genetic Analysis Workshop 17 exome-sequencing SNP data
Authors (first, second and last of 4)
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Detection of associations with rare and common SNPs for quantitative traits: a nonparametric Bayes-based approach
Authors (first, second and last of 6)
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Evaluation of a LASSO regression approach on the unrelated samples of Genetic Analysis Workshop 17
Authors
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Identification of functional genetic variation in exome sequence analysis
Authors (first, second and last of 7)
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Comparison of results from tests of association in unrelated individuals with uncollapsed and collapsed sequence variants using tiled regression
Authors (first, second and last of 10)
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Identifying rare disease variants in the Genetic Analysis Workshop 17 simulated data: a comparison of several statistical approaches
Authors (first, second and last of 5)
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Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set
Authors (first, second and last of 4)
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LASSO model selection with post-processing for a genome-wide association study data set
Authors (first, second and last of 4)
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Testing gene-environment interactions in gene-based association studies
Authors (first, second and last of 5)
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Detecting functional rare variants by collapsing and incorporating functional annotation in Genetic Analysis Workshop 17 mini-exome data
Authors (first, second and last of 6)
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Exploration and comparison of methods for combining population- and family-based genetic association using the Genetic Analysis Workshop 17 mini-exome
Authors (first, second and last of 6)
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Challenges and directions: an analysis of Genetic Analysis Workshop 17 data by collapsing rare variants within family data
Authors (first, second and last of 5)
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Comparison of genetic association strategies in the presence of rare alleles
Authors (first, second and last of 6)
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Comparative study of statistical methods for detecting association with rare variants in exome-resequencing data
Authors (first, second and last of 5)
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Estimating heritability using family and unrelated individuals data
Authors (first, second and last of 5)
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Methods for adjusting population structure and familial relatedness in association test for collective effect of multiple rare variants on quantitative traits
Authors (first, second and last of 5)
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Family- and population-based designs identify different rare causal variants
Authors (first, second and last of 6)
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Use of Bayesian networks to dissect the complexity of genetic disease: application to the Genetic Analysis Workshop 17 simulated data
Authors (first, second and last of 6)
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Using the posterior distribution of deviance to measure evidence of association for rare susceptibility variants
Authors (first, second and last of 4)
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Prioritizing single-nucleotide variations that potentially regulate alternative splicing
Authors (first, second and last of 7)
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Comparison of SNP-based and gene-based association studies in detecting rare variants using unrelated individuals
Authors (first, second and last of 4)
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Combining effects from rare and common genetic variants in an exome-wide association study of sequence data
Authors (first, second and last of 6)
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Pathway-based joint effects analysis of rare genetic variants using Genetic Analysis Workshop 17 exon sequence data
Authors (first, second and last of 5)
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Large-scale risk prediction applied to Genetic Analysis Workshop 17 mini-exome sequence data
Authors (first, second and last of 9)
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Evaluating methods for combining rare variant data in pathway-based tests of genetic association
Authors (first, second and last of 6)
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New insights into old methods for identifying causal rare variants
Authors (first, second and last of 5)
