Comparison of statistical tests for disease association with rare variants.
about
Beyond the fourth wave of genome-wide obesity association studiesTwo-phase and family-based designs for next-generation sequencing studiesRare-variant association analysis: study designs and statistical testsEvaluation of logistic Bayesian LASSO for identifying association with rare haplotypesStrategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyMutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological Sense.Introduction to deep sequencing and its application to drug addiction research with a focus on rare variants.A unified method for detecting secondary trait associations with rare variants: application to sequence data.A variational Bayes discrete mixture test for rare variant associationTesting for association with multiple traits in generalized estimation equations, with application to neuroimaging data.Family-based association tests for sequence data, and comparisons with population-based association tests.A variance component based multi-marker association test using family and unrelated data.Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured dataDetecting genomic clustering of risk variants from sequence data: cases versus controls.Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statisticVariant association tools for quality control and analysis of large-scale sequence and genotyping array dataMethods for collapsing multiple rare variants in whole-genome sequence data.Identifying rare and common disease associated variants in genomic data using Parkinson's disease as a model.Performance of statistical methods on CHARGE targeted sequencing dataHierarchical Bayesian model for rare variant association analysis integrating genotype uncertainty in human sequence data.Comparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data.Kullback-Leibler distance methods for detecting disease association with rare variants from sequencing data.Optimal tests for rare variant effects in sequencing association studies.Powerful association test combining rare variant and gene expression using family data from Genetic Analysis Workshop 19.The impact of rare and low-frequency genetic variants in common diseaseLongitudinal data analysis for rare variants detection with penalized quadratic inference functionHaplotype kernel association test as a powerful method to identify chromosomal regions harboring uncommon causal variants.Sequencing studies in human genetics: design and interpretation.Longitudinal analysis is more powerful than cross-sectional analysis in detecting genetic association with neuroimaging phenotypes.A powerful and adaptive association test for rare variantsSequence variation in TMEM18 in association with body mass index: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study.Identifying rare variants associated with hypertension using the C-alpha testOn the Aggregation of Multimarker Information for Marker-Set and Sequencing Data Analysis: Genotype Collapsing vs. Similarity Collapsing.Weighted selective collapsing strategy for detecting rare and common variants in genetic association study.Joint rare variant association test of the average and individual effects for sequencing studies.SEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations.Dynamic Bayesian testing of sets of variants in complex diseases.Comparison of similarity-based tests and pooling strategies for rare variantsProperties and modeling of GWAS when complex disease risk is due to non-complementing, deleterious mutations in genes of large effect.Targeted deep resequencing identifies coding variants in the PEAR1 gene that play a role in platelet aggregation.
P2860
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P2860
Comparison of statistical tests for disease association with rare variants.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Comparison of statistical tests for disease association with rare variants.
@en
type
label
Comparison of statistical tests for disease association with rare variants.
@en
prefLabel
Comparison of statistical tests for disease association with rare variants.
@en
P2860
P356
P1433
P1476
Comparison of statistical tests for disease association with rare variants.
@en
P2093
P2860
P304
P356
10.1002/GEPI.20609
P577
2011-07-18T00:00:00Z