Population-based and family-based designs to analyze rare variants in complex diseases. - Wikidata - awgldk - TriplyDB

Population-based and family-based designs to analyze rare variants in complex diseases.

Population-based and family-based designs to analyze rare variants in complex diseases.

http://www.wikidata.org/entity/Q41886407

about

Integrative cancer epidemiology--the next generation Adjusting family relatedness in data-driven burden test of rare variants Transmission and decorrelation methods for detecting rare variants using sequencing data from related individuals.Statistical methods for genome-wide and sequencing association studies of complex traits in related samples.Impact of Population Stratification on Family-Based Association in an Admixed Population Lessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysis Robust rare variant association testing for quantitative traits in samples with related individuals Identification of novel candidate variants including COL6A6 polymorphisms in early-onset atopic dermatitis using whole-exome sequencing GREB1 genetic variants are associated with bone mineral density in Caucasians.SNP Set Association Testing for Survival Outcomes in the Presence of Intrafamilial Correlation.Permutation testing in the presence of polygenic variation.Evaluation of Gene-Based Family-Based Methods to Detect Novel Genes Associated With Familial Late Onset Alzheimer Disease.Association of CDKAL1 Polymorphisms with Early-Onset Atopic Dermatitis in Koreans.

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Population-based and family-based designs to analyze rare variants in complex diseases.

http://www.wikidata.org/entity/Q41886407

description

2011 nî lūn-bûn

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2011年の論文

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2011年論文

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2011年論文

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2011年论文

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2011年论文

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name

Population-based and family-based designs to analyze rare variants in complex diseases.

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type

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Population-based and family-based designs to analyze rare variants in complex diseases.

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prefLabel

Population-based and family-based designs to analyze rare variants in complex diseases.

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Genetic Epidemiology

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Population-based and family-based designs to analyze rare variants in complex diseases.

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Julia N Bailey

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

Rémi Kazma

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A map of human genome variation from population-scale sequencing

Genomewide association studies and assessment of the risk of disease

Pooled association tests for rare variants in exon-resequencing studies

Common SNPs explain a large proportion of the heritability for human height

Personal genomes: The case of the missing heritability

Missing heritability and strategies for finding the underlying causes of complex disease

Multipoint quantitative-trait linkage analysis in general pedigrees

Genomic screening and replication using the same data set in family-based association testing.

Simple association analysis combining data from trios/sibships and unrelated controls.

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

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S41-7

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scholarly article

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10.1002/GEPI.20648

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35 Suppl 1

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2011-01-01T00:00:00Z

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221718249

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22128057

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3393851

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