A data-adaptive sum test for disease association with multiple common or rare variants.
about
In search of low-frequency and rare variants affecting complex traitsStatistical analysis for genome-wide association studyInsights into blood lipids from rare variant discoveryRare-variant association analysis: study designs and statistical testsComputational and statistical approaches to analyzing variants identified by exome sequencingProgress in methods for rare variant associationPleiotropy analysis of quantitative traits at gene level by multivariate functional linear modelsChallenges of Big Data AnalysisTargeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet diseaseA unified method for detecting secondary trait associations with rare variants: application to sequence data.Weighted pedigree-based statistics for testing the association of rare variantsA 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.Rare variant association testing for next-generation sequencing data via hierarchical clustering.A novel test for testing the optimally weighted combination of rare and common variants based on data of parents and affected children.A generalized genetic random field method for the genetic association analysis of sequencing data.A power set-based statistical selection procedure to locate susceptible rare variants associated with complex traits with sequencing data.Variant association tools for quality control and analysis of large-scale sequence and genotyping array dataTesting genetic association with rare and common variants in family data.Adjusting family relatedness in data-driven burden test of rare variantsIdentifying rare and common disease associated variants in genomic data using Parkinson's disease as a model.Review of current methods, applications, and data management for the bioinformatics analysis of whole exome sequencing.Whole genome sequencing data from pedigrees suggests linkage disequilibrium among rare variants created by population admixture.Higher criticism approach to detect rare variants using whole genome sequencing dataA generalized least-squares framework for rare-variant analysis in family dataAdaptive combination of P-values for family-based association testing with sequence dataRegion-Based Association Test for Familial Data under Functional Linear ModelsRare-Variant Kernel Machine Test for Longitudinal Data from Population and Family SamplesA new statistical framework for genetic pleiotropic analysis of high dimensional phenotype data.A powerful association test of multiple genetic variants using a random-effects model.The impact of rare and low-frequency genetic variants in common diseaseLongitudinal data analysis for rare variants detection with penalized quadratic inference functionComprehensive approach to analyzing rare genetic variantsKernel-machine testing coupled with a rank-truncation method for genetic pathway analysis.FLT1 genetic variation predisposes to neovascular AMD in ethnically diverse populations and alters systemic FLT1 expression.Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines.Detecting association of rare and common variants based on cross-validation prediction error.Rare-variant association testing for sequencing data with the sequence kernel association test.
P2860
Q24618492-419421DB-6B9E-45F9-951C-AF2DCB8C626FQ26799032-A1A563C8-BCF2-4771-A62B-17A92F77301DQ26799138-82A2E59E-439A-4C02-95BA-3014929BCFD6Q26852733-7DB0DF83-DF4A-47C4-AF03-393DC9F7E73CQ27024342-9A60BC1B-8589-4760-83D3-5E34DCBFE68EQ28601645-5FFCF8BE-7DB1-4515-9800-27BDB409F276Q28647065-D9341FE7-C28C-48F5-A1A2-7D1A056972B0Q28651981-AF071C36-325F-43E3-812D-F92D2DDEC199Q30447248-3B6CD54F-76F1-4418-ABC6-974DB79B91ECQ30578001-6E70274C-D41A-40D5-B63F-15D57B342181Q30578311-47D3E6B8-0526-41B2-ACDE-E5B2230746B2Q30578631-1A75EB21-A8D4-478D-91B0-4C4663F6FB2BQ30579877-9A40B30F-16B8-4E30-88CA-CC807514AED5Q30587122-FA779FD8-85B8-44D7-95A0-6152EB4892C5Q30599570-B5B58ECE-125A-4391-8F90-D3A2849F911CQ30617836-97F1AB34-A468-4CE5-94A7-7DA0BB24B7C5Q30725035-E648B4E9-2126-4DB2-8FE0-D0C9F411936DQ30746271-97E14F85-518B-4410-8C44-93FC88492EB4Q30806575-0538348B-98C5-4AEB-93D7-AB382491FF15Q30813514-FAB00F31-9ADF-455B-8116-70F36AB059C0Q30841941-AF72FBBA-618D-4C79-B0A1-EC077278A85CQ30846312-85A13938-59D8-40C0-93BC-6AB933366538Q30846819-85FD92AF-BB13-4FE0-A1C6-8E13E7CC3C49Q30857788-288347CB-3C30-47A3-B7E0-CE97917D980EQ30879476-6066831A-8A72-4ABF-AEC0-D253C0A15FACQ30879621-FDADA613-AE59-45F0-A768-416AD402A437Q30879675-776CFE9C-B184-469B-B641-099F7C0468B5Q30881935-433163EE-5F3F-42BE-8877-62E85502FB8BQ30976711-42DC0B62-2111-4D9C-8426-3D22BA84B5E4Q31094385-D0584109-BB5F-4DB2-B17E-9B074EACA479Q31141263-EB9B3A25-A125-4B2C-9D14-7017C4A83E76Q33560740-9728B015-106C-4785-B956-68C7C4475350Q33613854-93B9579E-8EA0-4FB4-9925-5045E421E590Q33677747-140BDAD6-C887-47F8-8BDB-292E3B895F44Q33745005-7D19413C-E955-4022-9D71-631CB310DC8AQ33814014-4BDB2149-3AF0-4E39-AF51-283146D4E43EQ33816926-5C11E342-DC2C-4A0F-8080-090CECCD0FC2Q33839446-EB059552-48A9-41E7-8917-9B3FAF026BB8Q33887770-71CA60AD-3FE9-4ABA-90A0-CC7F5798A795Q33954046-61AD7635-C578-4AD9-9928-445F7A4F0959
P2860
A data-adaptive sum test for disease association with multiple common or rare variants.
description
2010 nî lūn-bûn
@nan
2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
A data-adaptive sum test for disease association with multiple common or rare variants.
@ast
A data-adaptive sum test for disease association with multiple common or rare variants.
@en
A data-adaptive sum test for disease association with multiple common or rare variants.
@nl
type
label
A data-adaptive sum test for disease association with multiple common or rare variants.
@ast
A data-adaptive sum test for disease association with multiple common or rare variants.
@en
A data-adaptive sum test for disease association with multiple common or rare variants.
@nl
prefLabel
A data-adaptive sum test for disease association with multiple common or rare variants.
@ast
A data-adaptive sum test for disease association with multiple common or rare variants.
@en
A data-adaptive sum test for disease association with multiple common or rare variants.
@nl
P2860
P356
P1433
P1476
A data-adaptive sum test for disease association with multiple common or rare variants.
@en
P2093
P2860
P356
10.1159/000288704
P577
2010-04-23T00:00:00Z