Optimal tests for rare variant effects in sequencing association studies. - Wikidata - awgldk - TriplyDB

Optimal tests for rare variant effects in sequencing association studies.

Optimal tests for rare variant effects in sequencing association studies.

http://www.wikidata.org/entity/Q31065241

about

Insights into blood lipids from rare variant discovery Rare-variant association analysis: study designs and statistical tests Rationale, design and baseline results of the Guangxi manganese-exposed workers healthy cohort (GXMEWHC) study Whole exome sequencing identifies novel genes for fetal hemoglobin response to hydroxyurea in children with sickle cell anemia TYK2 protein-coding variants protect against rheumatoid arthritis and autoimmunity, with no evidence of major pleiotropic effects on non-autoimmune complex traits Exome Analyses of Long QT Syndrome Reveal Candidate Pathogenic Mutations in Calmodulin-Interacting Genes Genome-Wide Association Study in Immunocompetent Patients with Delayed Hypersensitivity to Sulfonamide Antimicrobials Progress in methods for rare variant association The power of meta-analysis in genome-wide association studies The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation The genetic architecture of type 2 diabetes Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure.A variational Bayes discrete mixture test for rare variant association Family-based association tests for sequence data, and comparisons with population-based association tests.Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured data Detecting genomic clustering of risk variants from sequence data: cases versus controls.Scan statistic-based analysis of exome sequencing data identifies FAN1 at 15q13.3 as a susceptibility gene for schizophrenia and autism Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland.Kernel methods for large-scale genomic data analysis.Testing genetic association with rare and common variants in family data.A weighted U-statistic for genetic association analyses of sequencing data.Comparing the power of family-based association tests for sequence data with applications in the GAW18 simulated data.Evaluation of gene-based association tests for analyzing rare variants using Genetic Analysis Workshop 18 data.Adaptive combination of P-values for family-based association testing with sequence data Kullback-Leibler distance methods for detecting disease association with rare variants from sequencing data.Region-Based Association Test for Familial Data under Functional Linear Models Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family Samples Detecting multiple variants associated with disease based on sequencing data of case-parent trios.A powerful and efficient set test for genetic markers that handles confounders A unified powerful set-based test for sequencing data analysis of GxE interactions.Region-based association analysis of human quantitative traits in related individuals.A W-test collapsing method for rare-variant association testing in exome sequencing data.Gene-set association tests for next-generation sequencing data On combining family- and population-based sequencing 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 Samples GEE-based SNP set association test for continuous and discrete traits in family-based association studies Exome-wide association study of endometrial cancer in a multiethnic population Knowledge-driven binning approach for rare variant association analysis: application to neuroimaging biomarkers in Alzheimer's disease

P2860

Q26799138-1F6BD610-45CD-4F1A-A4BA-0F58EE5D5485 Q26852733-DCA4ECBD-0F6B-433A-AF61-06B19F6C5657 Q28389898-F5C757F7-FE4A-46F1-A5F7-E531A698541D Q28544643-E62AE65A-AFFA-41BA-BF51-8EDE4FADFE51 Q28545832-CFE618A7-EE05-4AD0-8A42-90E9BFE58D8D Q28546038-D5663BF6-2F4E-4E39-B368-B68130E39786 Q28550088-648C3C97-58B9-459C-8943-708069D6D7D1 Q28601645-D32293E3-499F-424F-8900-F257C3C5640D Q28658972-6BC8C141-E9AF-4D79-B75C-4369335942D6 Q28685216-A760FC42-6454-4AD9-BA5F-B5EF3AF2E2A8 Q29583824-AF6BA146-C089-44DF-B99E-590C40AC17F7 Q30252611-36E0A810-A9D9-440E-9176-601AA1376550 Q30252853-4C3A1447-4CAB-4557-A783-C2E3B7579AA1 Q30578631-B0F4D532-11FC-4370-9A8A-9C4B5A1DD1A4 Q30587122-46813236-FFD7-475F-B9D3-2197727DBFC4 Q30621608-1E46A76A-4AD2-4BDB-8DEC-612BA2D4C890 Q30654520-CE2F84B1-E9BE-4A5A-86BE-2AC83778AC83 Q30717096-93E71C69-243D-4E8B-BBBF-243B2B88B8F4 Q30800931-E9BF00BD-D01A-4C86-B027-8B3D45276D02 Q30809578-33193D9B-E125-4963-ADD2-6D949DE53600 Q30838088-9A85CA38-E3F4-40A0-820F-EA5803F25126 Q30841941-6F871139-4B76-43AA-8D78-7935ECEBF9BA Q30863151-185FCE3B-1355-43B5-887A-FC35D25DF2C2 Q30879444-355B43BB-C815-4FE0-9C3C-16420FEAC6F4 Q30879961-C3B833F1-E9E2-4BAB-B3D6-4442620E43CA Q30881935-6DFB2256-26C2-4DF8-8E1F-F673AE23F3F3 Q30932501-65964AA5-039E-456E-8178-C135619417D5 Q30976711-BFDC7760-9E12-4F48-9590-EDFE94FE337E Q31094385-E07D0C91-25AA-44F3-B3BB-2B9FB8274B6C Q31106613-F6E69153-9F77-45E8-B044-96A79AA933EB Q31115587-8958E210-B084-4EAE-915F-70DE1C314E75 Q31118526-A4CD3829-5743-4305-93F4-7F35287CEDB9 Q31120147-9BB60CC4-7CD3-43B9-81A1-C3C1C9036CD8 Q31121956-B55ECF16-79D7-4E6D-8FDE-77B0B251BD03 Q31126299-71611CD9-F2DE-4318-8DB9-AC75A5683ED8 Q31149244-4C8D364A-F1BB-46F3-B3EE-B1F186F54261 Q31166205-F388921C-511E-4B70-A5FB-FF3B821549BA Q33556485-94865D92-7BD3-46C4-9DE0-165AE50D07EE Q33584276-3045A449-F66E-4D96-A839-DB7127AB7030 Q33726449-AC4F2EEC-1B8C-4873-9D6D-A85E71D17D71

P2860

Optimal tests for rare variant effects in sequencing association studies.

http://www.wikidata.org/entity/Q31065241

description

2012 nî lūn-bûn

@nan

2012 թուականի Յունիսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի հունիսին 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

Optimal tests for rare variant effects in sequencing association studies.

@ast

Optimal tests for rare variant effects in sequencing association studies.

@en

type

label

Optimal tests for rare variant effects in sequencing association studies.

@ast

Optimal tests for rare variant effects in sequencing association studies.

@en

prefLabel

Optimal tests for rare variant effects in sequencing association studies.

@ast

Optimal tests for rare variant effects in sequencing association studies.

@en

P1433

Q31065241-CB861EC1-F74B-4AA3-A509-9622D05B8902

P1476

Q31065241-BF57C6B7-B716-4EE2-BE91-D32FE28A3D28

P2093

Q31065241-1B9D167B-CAD4-4D60-8A05-EA3E0987E9F6

Q31065241-2C5E12C5-BB4B-4EA7-B7CE-42CA383BD411

Q31065241-F1A82CF3-528E-4CBA-AE69-5C0B65460EDD

P2860

Q31065241-05AB2A88-8AA9-478E-A7F4-777ED9B001D5

Q31065241-06EBCA9F-4D5B-4D86-8E64-E873A88599B4

Q31065241-09D15D98-E387-44DD-913E-1B6BF7D8FF79

Q31065241-27FF9725-A497-4351-8E97-606702733981

Q31065241-28B18CE7-5903-49AD-AEEF-29ECFA2AD3AD

Q31065241-39EDAB5B-FB17-4592-A651-0E28B0CD1C4E

Q31065241-4812F5D5-42E9-4358-A255-F2A9206EA91B

Q31065241-4868FF0E-BF78-435D-A057-ED131117486A

Q31065241-53D10897-6153-4988-B5A3-2F201375BE50

Q31065241-70F5C07F-5B2F-4011-96EF-D27ACCBBF178

P304

Q31065241-27C9BAC3-05F4-45DD-8733-9F6FA8C1CFE9

P31

Q31065241-10E3C7D7-A212-4EB7-B04A-57C6B15EDB5A

P356

Q31065241-F5A3B20F-6C68-4D1C-86A6-85D4CB1BDF8C

P433

Q31065241-EDAD534C-73DD-4483-9ED0-44A8F336B6E5

P478

Q31065241-5B53A7D2-6BCD-489F-A62F-31F67A8D06E3

P577

Q31065241-4A764DFD-B161-4492-9CFA-EE97B8C14025

P5875

Q31065241-C7B00E2F-45E6-4F41-A637-08BC530FB9ED

P698

Q31065241-BD995340-398B-4029-9CDB-EDB246351650

P932

Q31065241-7CB1B60F-CEB7-45B1-B03B-2DAA79DE0F52

P356

P1433

P1476

Optimal tests for rare variant effects in sequencing association studies.

@en

P2093

Michael C Wu

http://www.w3.org/2001/XMLSchema#string

Seunggeun Lee

http://www.w3.org/2001/XMLSchema#string

Xihong Lin

http://www.w3.org/2001/XMLSchema#string

P2860

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

Pooled association tests for rare variants in exon-resequencing studies

Semiparametric regression of multidimensional genetic pathway data: least-squares kernel machines and linear mixed models

Estimation and testing for the effect of a genetic pathway on a disease outcome using logistic kernel machine regression via logistic mixed models.

Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data.

A groupwise association test for rare mutations using a weighted sum statistic.

Testing for an unusual distribution of rare variants.

Rare-variant association testing for sequencing data with the sequence kernel association test.

Most rare missense alleles are deleterious in humans: implications for complex disease and association studies.

Haplotype-based association analysis via variance-components score test.

P304

762-775

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1093/BIOSTATISTICS/KXS014

http://www.w3.org/2001/XMLSchema#string

P433

4

http://www.w3.org/2001/XMLSchema#string

P478

13

http://www.w3.org/2001/XMLSchema#string

P577

2012-06-14T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

225374683

http://www.w3.org/2001/XMLSchema#string

P698

22699862

http://www.w3.org/2001/XMLSchema#string

P932

3440237

http://www.w3.org/2001/XMLSchema#string