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Insights into blood lipids from rare variant discoveryTwo-phase and family-based designs for next-generation sequencing studiesRare-variant association analysis: study designs and statistical testsComputational and statistical approaches to analyzing variants identified by exome sequencingExome sequencing and complex disease: practical aspects of rare variant association studiesEvaluation of logistic Bayesian LASSO for identifying association with rare haplotypesPatterns and rates of exonic de novo mutations in autism spectrum disordersProgress in methods for rare variant associationPleiotropy analysis of quantitative traits at gene level by multivariate functional linear modelsApplication of noncollapsing methods to the gene-based association test: a comparison study using Genetic Analysis Workshop 18 dataA primer for disease gene prioritization using next-generation sequencing dataThe Growing Importance of CNVs: New Insights for Detection and Clinical InterpretationDissecting the genetics of complex traits using summary association statisticsRare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer.Mutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological Sense.In Silico Functional Annotation of Genomic Variation.Sequencing of Charcot-Marie-Tooth disease genes in a toxic polyneuropathy.Introduction to deep sequencing and its application to drug addiction research with a focus on rare variants.Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression.Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet diseaseWeighted pedigree-based statistics for testing the association of rare variantsMultiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured dataRegularized rare variant enrichment analysis for case-control exome sequencing data.A novel test for testing the optimally weighted combination of rare and common variants based on data of parents and affected children.Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statisticSimulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland.Variant association tools for quality control and analysis of large-scale sequence and genotyping array dataA unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data.Next Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data.Methods for collapsing multiple rare variants in whole-genome sequence data.Testing genetic association with rare and common variants in family data.Adjusting family relatedness in data-driven burden test of rare variantsFamily-based association test using both common and rare variants and accounting for directions of effects for sequencing data.Review of current methods, applications, and data management for the bioinformatics analysis of whole exome sequencing.A weighted U-statistic for genetic association analyses of sequencing data.Hierarchical Bayesian model for rare variant association analysis integrating genotype uncertainty in human sequence data.Analysis of Genetic Analysis Workshop 18 data with gene-based penalized regression.Whole genome sequencing data from pedigrees suggests linkage disequilibrium among rare variants created by population admixture.Rare variant analysis of blood pressure phenotypes in the Genetic Analysis Workshop 18 whole genome sequencing data using sequence kernel association test.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մարտին հրատարակված գիտական հոդված
@hy
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
name
Testing for an unusual distribution of rare variants.
@ast
Testing for an unusual distribution of rare variants.
@en
type
label
Testing for an unusual distribution of rare variants.
@ast
Testing for an unusual distribution of rare variants.
@en
prefLabel
Testing for an unusual distribution of rare variants.
@ast
Testing for an unusual distribution of rare variants.
@en
P2093
P2860
P50
P1433
P1476
Testing for an unusual distribution of rare variants.
@en
P2093
Benjamin M Neale
Bernie Devlin
Manuel A Rivas
Shaun M Purcell
P2860
P304
P356
10.1371/JOURNAL.PGEN.1001322
P50
P577
2011-03-03T00:00:00Z