about
Genetic linkage analysis in the age of whole-genome sequencingGenomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolateFamily-based association tests for sequence data, and comparisons with population-based association tests.A novel test for testing the optimally weighted combination of rare and common variants based on data of parents and affected children.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.Family-based association test using both common and rare variants and accounting for directions of effects for sequencing data.Comparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data.A comparative analysis of family-based and population-based association tests using whole genome sequence data.Adaptive combination of P-values for family-based association testing with sequence dataGeneration of sequence-based data for pedigree-segregating Mendelian or Complex traits.Detecting multiple variants associated with disease based on sequencing data of case-parent trios.Adjusting for Familial Relatedness in the Analysis of GWAS Data.Transmission and decorrelation methods for detecting rare variants using sequencing data from related individuals.A combined association test for rare variants using family and case-control data.The Rare-Variant Generalized Disequilibrium Test for Association Analysis of Nuclear and Extended Pedigrees with Application to Alzheimer Disease WGS Data.On the association analysis of genome-sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows.Utilizing population controls in rare-variant case-parent association testsThe power comparison of the haplotype-based collapsing tests and the variant-based collapsing tests for detecting rare variants in pedigrees.FamLBL: detecting rare haplotype disease association based on common SNPs using case-parent triadsThe rare TREM2 R47H variant exerts only a modest effect on Alzheimer disease risk.Complex pedigrees in the sequencing era: to track transmissions or decorrelate?SeqSIMLA: a sequence and phenotype simulation tool for complex disease studiesTwo-stage family-based designs for sequencing studies.On family-based genome-wide association studies with large pedigrees: observations and recommendations.A haplotype-based framework for group-wise transmission/disequilibrium tests for rare variant association analysisRobust and Powerful Affected Sibpair Test for Rare Variant Association.Family-based approaches: design, imputation, analysis, and beyond.FamPipe: An Automatic Analysis Pipeline for Analyzing Sequencing Data in Families for Disease StudiesDetecting associations of rare variants with common diseases: collapsing or haplotyping?Testing rare variants for hypertension using family-based tests with different weighting schemesRegion-based association tests for sequencing data on survival traits.IRF6 mutation screening in non-syndromic orofacial clefting: analysis of 1521 familiesHaptoglobin (HP) and Haptoglobin-related protein (HPR) copy number variation, natural selection, and trypanosomiasis.Blocking approach for identification of rare variants in family-based association studies.Utilising family-based designs for detecting rare variant disease associations.Associating rare genetic variants with human diseases.Pathway-based approach using hierarchical components of collapsed rare variants.Generalization of Rare Variant Association Tests for Longitudinal Family Studies.Genetic Epidemiology and Public Health: The Evolution From Theory to Technology.
P2860
Q27027718-9A0A101F-337A-46F8-AF22-2EC10826453BQ28657831-ADA6A742-899C-43E7-86AF-30D267A42DF9Q30587122-159AF857-B590-4879-AD22-9189AA6CBB87Q30725035-EA161050-1E90-4A14-87AE-96175EE39522Q30846312-A93222D4-8920-4E5D-A66D-704A3D9D24D5Q30846819-D138BEDE-4EE0-4F27-A792-57488BBED930Q30854460-B7560295-DA8B-4EF5-B619-BE913049F57DQ30879444-5AFA276A-748D-4D2F-8840-304753318711Q30879700-F07D1D16-581A-4380-8A42-94D96737753CQ30881935-CC190EF0-14FA-4856-A04D-A921EC945FF4Q30980733-1B83532E-4FDA-4E51-9B56-6AB66EACE554Q31106613-5521793E-4D6F-4188-9E5C-ACCEA617A26AQ31145284-5063EE30-110E-4333-B95F-A6E1F88B8723Q31149251-1A9F61B9-D9D7-4A7E-9764-0CEF0B3B804CQ31149253-3D0B1475-C357-45F8-AD62-7E1F48C96517Q31153544-88C6A5CB-DEE9-48CC-8728-A53A46067806Q33925543-5880346C-4B53-46DA-9B03-81818E474EBFQ34000914-19EAF5B2-C4E2-42F9-9291-713D5C32DFE9Q34037854-C569A44F-720F-47F1-968D-8B7D72C67940Q34136901-22189791-D78D-4A70-AB4D-CD2E01BE119CQ34303825-58A0645B-144E-45DD-9DE6-513ADC425EBCQ34743725-84A86AC0-22B9-417C-8F83-9B3D40917502Q34778042-4E885396-DA84-4ABF-887D-F9DE8250818EQ35527971-185DA048-D1B9-4A44-8E2A-5B57C4F34AD0Q35528411-275554C2-9E41-45AF-8CF5-C9BE973BA8BAQ35541152-E6E7F140-7235-43C5-B0FF-2D5D9EBF8BA4Q35748549-E513E12E-78F0-464E-A58B-D261EF135C38Q35920732-7FA91BE8-C4F9-46D3-B9F4-2CDA5267B1A3Q36043750-23AD435D-DD29-4E86-9B04-EA4114FCC1B7Q36060594-E404AC63-BFA2-4FE6-BC3F-523431893095Q36226069-CF0DA297-90D6-4DB3-97C7-3CA9107BD9A4Q36392512-36AEAD85-D638-498F-A914-24F32FE47906Q36665214-46C44671-8B1D-4B62-9CB5-92FD3FAF8630Q37502627-446B20A4-8180-4ADC-8E00-B6DD403E83C5Q37509918-76BD8FC0-A3ED-4B3B-AE7D-55B3867DAFDEQ39368271-74B4C104-D309-4AB1-9E0B-BE69D52E4219Q39382116-6A29D813-0D98-4CF5-A6ED-DD53EC462794Q39429370-509E4F4F-5333-4EEE-99AD-D3BE85AB8565Q40090917-D4EED735-585E-4849-BE44-B5E7B10F0CD4Q40893703-5DFE7D19-15EA-463F-AC0F-47EAF97C4ED8
P2860
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Rare variant analysis for family-based design.
@ast
Rare variant analysis for family-based design.
@en
Rare variant analysis for family-based design.
@nl
type
label
Rare variant analysis for family-based design.
@ast
Rare variant analysis for family-based design.
@en
Rare variant analysis for family-based design.
@nl
prefLabel
Rare variant analysis for family-based design.
@ast
Rare variant analysis for family-based design.
@en
Rare variant analysis for family-based design.
@nl
P2860
P1433
P1476
Rare variant analysis for family-based design.
@en
P2093
P2860
P304
P356
10.1371/JOURNAL.PONE.0048495
P407
P577
2013-01-15T00:00:00Z