The empirical power of rare variant association methods: results from sanger sequencing in 1,998 individuals.
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Insights into blood lipids from rare variant discoveryProgress in methods for rare variant associationWhole-genome sequencing identifies EN1 as a determinant of bone density and fracture.A unified method for detecting secondary trait associations with rare variants: application to sequence data.Statistical Approaches to Combine Genetic Association Data.Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data.Variant association tools for quality control and analysis of large-scale sequence and genotyping array dataIdentifying rare and common disease associated variants in genomic data using Parkinson's disease as a model.Performance of statistical methods on CHARGE targeted sequencing dataA 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.Gene analysis for longitudinal family data using random-effects models.Integrative analysis of functional genomic annotations and sequencing data to identify rare causal variants via hierarchical modeling.Gene-set association tests for next-generation sequencing dataGWAS to Sequencing: Divergence in Study Design and AnalysisGenetic variants including markers from the exome chip and metabolite traits of type 2 diabetes.On the association analysis of genome-sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows.Sequencing studies in human genetics: design and interpretation.A rare variant association test based on combinations of single-variant tests.SEQCHIP: a powerful method to integrate sequence and genotype data for the detection of rare variant associations.Multiple regression methods show great potential for rare variant association tests.A hybrid likelihood model for sequence-based disease association studies.Properties and modeling of GWAS when complex disease risk is due to non-complementing, deleterious mutations in genes of large effect.Assessing the impact of differential genotyping errors on rare variant tests of association.Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.BioBin: a bioinformatics tool for automating the binning of rare variants using publicly available biological knowledge.Bayesian detection of causal rare variants under posterior consistencyPerformance of genotype imputation for low frequency and rare variants from the 1000 genomesA genome-wide association study of seed protein and oil content in soybean.Converging evidence implicates the abnormal microRNA system in schizophreniaThe power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex diseaseKNOWLEDGE DRIVEN BINNING AND PHEWAS ANALYSIS IN MARSHFIELD PERSONALIZED MEDICINE RESEARCH PROJECT USING BIOBINAccurate Imputation-Based Screening of Gln368Ter Myocilin Variant in Primary Open-Angle Glaucoma.A Protein Domain and Family Based Approach to Rare Variant Association AnalysisDetecting associations of rare variants with common diseases: collapsing or haplotyping?Phenotypic Characterization and Genetic Dissection of Growth Period Traits in Soybean (Glycine max) Using Association Mapping.Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy.AP-SKAT: highly-efficient genome-wide rare variant association test.Comparison of single-marker and multi-marker tests in rare variant association studies of quantitative traits.
P2860
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P2860
The empirical power of rare variant association methods: results from sanger sequencing in 1,998 individuals.
description
2012 nî lūn-bûn
@nan
2012 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
The empirical power of rare va ...... quencing in 1,998 individuals.
@ast
The empirical power of rare va ...... quencing in 1,998 individuals.
@en
The empirical power of rare va ...... quencing in 1,998 individuals.
@nl
type
label
The empirical power of rare va ...... quencing in 1,998 individuals.
@ast
The empirical power of rare va ...... quencing in 1,998 individuals.
@en
The empirical power of rare va ...... quencing in 1,998 individuals.
@nl
prefLabel
The empirical power of rare va ...... quencing in 1,998 individuals.
@ast
The empirical power of rare va ...... quencing in 1,998 individuals.
@en
The empirical power of rare va ...... quencing in 1,998 individuals.
@nl
P2093
P2860
P1433
P1476
The empirical power of rare va ...... quencing in 1,998 individuals.
@en
P2093
Celia M T Greenwood
J Brent Richards
Martin Ladouceur
Zari Dastani
P2860
P304
P356
10.1371/JOURNAL.PGEN.1002496
P577
2012-02-02T00:00:00Z