Sequence kernel association test for quantitative traits in family samples
about
Two-phase and family-based designs for next-generation sequencing studiesRare-variant association analysis: study designs and statistical testsCombining family- and population-based imputation data for association analysis of rare and common variants in large pedigreesProgress in methods for rare variant associationApplication of noncollapsing methods to the gene-based association test: a comparison study using Genetic Analysis Workshop 18 dataSequencing of 2 subclinical atherosclerosis candidate regions in 3669 individuals: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyStrategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyAssociation of levels of fasting glucose and insulin with rare variants at the chromosome 11p11.2-MADD locus: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyGenetic Modifiers of Age at Onset in Carriers of the G206A Mutation in PSEN1 With Familial Alzheimer Disease Among Caribbean Hispanics.Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.Introduction to deep sequencing and its application to drug addiction research with a focus on rare variants.Challenges of linkage analysis in the era of whole-genome sequencing.Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colorsMultiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured dataA novel test for testing the optimally weighted combination of rare and common variants based on data of parents and affected children.Kernel methods for large-scale genomic data analysis.Testing genetic association with rare and common variants in family data.Adjusting family relatedness in data-driven burden test of rare variantsComparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data.Rare variant analysis of blood pressure phenotypes in the Genetic Analysis Workshop 18 whole genome sequencing data using sequence kernel association test.Adaptive combination of P-values for family-based association testing with sequence dataThe role of rare variants in systolic blood pressure: analysis of ExomeChip data in HyperGEN African AmericansRegion-Based Association Test for Familial Data under Functional Linear ModelsPBAP: a pipeline for file processing and quality control of pedigree data with dense genetic markersExome Sequence Data From Multigenerational Families Implicate AMPA Receptor Trafficking in Neurocognitive Impairment and Schizophrenia Risk.Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family SamplesOn combining family- and population-based sequencing dataA combined association test for rare variants using family and case-control data.Incorporating ENCODE information into association analysis of whole genome sequencing data.Comparing strategies for combined testing of rare and common variants in whole sequence and genome-wide genotype data.The Weighting is the Hardest Part: On the Behavior of the Likelihood Ratio Test and the Score Test Under a Data-Driven Weighting Scheme in Sequenced SamplesSequence robust association test for familial data.GEE-based SNP set association test for continuous and discrete traits in family-based association studiesJoint genetic analysis using variant sets reveals polygenic gene-context interactions.The power comparison of the haplotype-based collapsing tests and the variant-based collapsing tests for detecting rare variants in pedigrees.Flexible and robust methods for rare-variant testing of quantitative traits in trios and nuclear families.Sequence kernel association test for survival traits.Greater power and computational efficiency for kernel-based association testing of sets of genetic variants.Sequencing of LRP2 reveals multiple rare variants associated with urinary trefoil factor-3.Complex pedigrees in the sequencing era: to track transmissions or decorrelate?
P2860
Q26828744-342F97D0-6923-4294-8814-46BC018D7F5CQ26852733-C88B1099-D222-4578-891A-DF84A749C3B3Q28395566-F4906308-395F-4914-A223-FAD8A896437EQ28601645-A416F2DA-B11E-4750-92FD-04641E38C284Q28654278-D877D746-DF8F-4B55-A9CB-11C11E1526BAQ28655273-A065A489-23E9-4F0B-BF17-80710AD14E3BQ28655423-1FF4EBB9-50C1-4DAD-8C46-A268AA7AD593Q28657819-00E54F98-DB3A-47AB-A5E4-9384AEAC1764Q30009136-AEE5736A-546E-41E4-BD53-05641B96CA62Q30252853-ABF7364C-8915-4BEC-8DE3-D265733CABC8Q30408390-8D4866D6-1AB5-4197-AFB2-0847B0D5B5ADQ30487212-43F39FF8-6644-414B-B0D4-61302D6FC7ADQ30580481-E04992B7-65D6-44BE-BD68-653A8FCCB700Q30621608-6D472462-38A6-4B98-93D1-29EBD49AC26BQ30725035-AFE17A9B-B8B2-475D-9AEB-6A7E1380F775Q30838088-8BAF0816-97D9-4DB9-B680-957EAE3173F8Q30841941-B6A3E313-2AA4-4725-B653-D2BD42CCA9C3Q30846312-6CA66E45-341D-41D2-9B62-A32689521C59Q30879444-99DBCAAA-7D64-4B7B-A77C-062BEFF0AABAQ30879542-F13FC291-9AF9-4785-8AA9-E4E5AF8BE297Q30881935-90C78BB2-12C6-4CDD-8424-9A7DE6F4D19FQ30909399-9BF946C7-77A6-457C-9531-0B57570580A6Q30976711-8E990782-98BB-4325-92C2-D71FA8AA0B2AQ30984320-CEBE5B80-C4D1-4DBD-911F-DBB8571756D6Q30997126-FEDC7913-D75A-4627-ADF8-18B67F16B49EQ31094385-CCD4C00C-5F57-491B-A269-70BE349A405EQ31149244-2A081753-3695-4AB3-B85E-20818194481FQ31149253-BDDCF342-9AC5-4886-A8CB-A25D47C76DD3Q31149262-C581BF0F-15DE-4D1D-8BCA-C063B01EE7DEQ31149266-17DFB7C0-10C9-4A3B-860D-85D2BECE7E5CQ31166205-F0B40C29-57DF-4DED-90FC-64C67B613578Q31172609-9655C1EE-25E3-4558-AC80-26AE4BB8A899Q33556485-7FA4F3C6-AF5A-495D-A352-9A9D1F26B7ECQ33584485-58D20702-9CEB-4053-9186-2E5F3FF13ADBQ34037854-5AC322AA-B233-4C84-A540-65F45B970A00Q34068202-462A07B4-C18B-447D-B328-0F11DA57AA5AQ34154446-A7D9880F-99EF-44B2-B7DE-8E0B4304A6A0Q34456687-30529219-F333-4082-9E6C-DA37E846D768Q34568802-DDBD737A-8EA2-43A3-81E4-1E5C65AB145BQ34743725-56C436B4-63AC-4CF2-9141-E522ED798C66
P2860
Sequence kernel association test for quantitative traits in family samples
description
2012 nî lūn-bûn
@nan
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
2012年论文
@zh
2012年论文
@zh-cn
name
Sequence kernel association test for quantitative traits in family samples
@ast
Sequence kernel association test for quantitative traits in family samples
@en
type
label
Sequence kernel association test for quantitative traits in family samples
@ast
Sequence kernel association test for quantitative traits in family samples
@en
prefLabel
Sequence kernel association test for quantitative traits in family samples
@ast
Sequence kernel association test for quantitative traits in family samples
@en
P2860
P50
P356
P1433
P1476
Sequence kernel association test for quantitative traits in family samples
@en
P2860
P304
P356
10.1002/GEPI.21703
P577
2012-12-26T00:00:00Z