Results: 1199
Identifying rare variants using a Bayesian regression approach.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S99
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Finding genes that influence quantitative traits with tree-based clustering.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S98
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Addition of multiple rare SNPs to known common variants improves the association between disease and gene in the Genetic Analysis Workshop 17 data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S97
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Detecting disease rare alleles using single SNPs in families and haplotyping in unrelated subjects from the Genetic Analysis Workshop 17 data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S96
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Search for compound heterozygous effects in exome sequence of unrelated subjects.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S95
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Rare variant collapsing in conjunction with mean log p-value and gradient boosting approaches applied to Genetic Analysis Workshop 17 data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S94
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Analysis of human mini-exome sequencing data from Genetic Analysis Workshop 17 using a Bayesian hierarchical mixture model.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S93
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Penalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S92
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SNP set analysis for detecting disease association using exon sequence data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S91
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Does pathway analysis make it easier for common variants to tag rare ones?
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S90
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- Article
Pairwise shared genomic segment analysis in high-risk pedigrees: application to Genetic Analysis Workshop 17 exome-sequencing SNP data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S9
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Association tests for rare and common variants based on genotypic and phenotypic measures of similarity between individuals.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S89
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- Article
Capability of common SNPs to tag rare variants.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S88
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- Article
Do rare variant genotypes predict common variant genotypes?
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S87
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- Article
Linkage analysis merging replicate phenotypes: an application to three quantitative phenotypes in two African samples.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S81
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- Article
A pathway-based association analysis model using common and rare variants.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S85
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- Article
A method to detect single-nucleotide polymorphisms accounting for a linkage signal using covariate-based affected relative pair linkage analysis.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S84
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- Article
Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S83
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- Article
Enriching rare variants using family-specific linkage information.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S82
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Evaluation of association tests for rare variants using simulated data sets in the Genetic Analysis Workshop 17 data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S86
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- Article
A novel method to detect rare variants using both family and unrelated case-control data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S80
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Population structure analysis using rare and common functional variants.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S8
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Using linkage analysis of large pedigrees to guide association analyses.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S79
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- Article
Different approaches for dealing with rare variants in family-based genetic studies: application of a Genetic Analysis Workshop 17 problem.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S78
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Strategies for selection of subjects for sequencing after detection of a linkage peak.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S77
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- Article
Identity-by-descent filtering as a tool for the identification of disease alleles in exome sequence data from distant relatives.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S76
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- Article
Gene-based multiple trait analysis for exome sequencing data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S75
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- Article
Joint association analysis of bivariate quantitative and qualitative traits.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S74
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- Article
Integrating binary traits with quantitative phenotypes for association mapping of multivariate phenotypes.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S73
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- Article
Genetic signal maximization using environmental regression.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S72
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- Article
Propensity score analysis in the Genetic Analysis Workshop 17 simulated data set on independent individuals.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S71
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- Article
Detecting rare functional variants using a wavelet-based test on quantitative and qualitative traits.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S70
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- Article
A gene-based approach for testing association of rare alleles.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S7
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Using LASSO regression to detect predictive aggregate effects in genetic studies.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S69
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- Article
Identifying variants that contribute to linkage for dichotomous and quantitative traits in extended pedigrees.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S68
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- Article
Regularized regression method for genome-wide association studies.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S67
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- Article
Principal components ancestry adjustment for Genetic Analysis Workshop 17 data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S66
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- Article
Gene-based Higher Criticism methods for largescale exonic single-nucleotide polymorphism data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S65
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- Article
Two-stage study designs combining genomewide association studies, tag single-nucleotide polymorphisms, and exome sequencing: accuracy of genetic effect estimates.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S64
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- Article
Power of association tests in the presence of multiple causal variants.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S63
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- Article
Case-control association testing by graphical modeling for the Genetic Analysis Workshop 17 mini-exome sequence data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S62
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- Article
Disease risk prediction with rare and common variants.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S61
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- Article
Treating phenotype as given: a simple resampling method for genome-wide association studies.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S60
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- Article
A weighted accumulation test for associating rare genetic variation with quantitative phenotypes.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S6
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Resampling procedures to identify important SNPs using a consensus approach.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S59
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Confidence set of putative quantitative trait loci in whole genome scans with application to the Genetic Analysis Workshop 17 simulated data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S58
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Application of Bayesian regression with singular value decomposition method in association studies for sequence data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S57
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- Article
Identification of functional rare variants in genome-wide association studies using stability selection based on random collapsing.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S56
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- Article
Mutational load analysis of unrelated individuals.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S55
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- Publication type:
- Article
Distance-based phenotypic association analysis of DNA sequence data.
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- BMC Proceedings, 2011, v. 5, n. Suppl 9, p. 1, doi. 10.1186/1753-6561-5-S9-S54
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