ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing data.
about
In search of low-frequency and rare variants affecting complex traitsInsights into blood lipids from rare variant discoveryRare-variant association analysis: study designs and statistical testsProgress in methods for rare variant associationThe Growing Importance of CNVs: New Insights for Detection and Clinical InterpretationRare variant association testing for next-generation sequencing data via hierarchical clustering.Next Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data.Whole exome re-sequencing implicates CCDC38 and cilia structure and function in resistance to smoking related airflow obstruction.The impact of rare and low-frequency genetic variants in common diseaseRare SERINC2 variants are specific for alcohol dependence in individuals of European descentWeighted Score Tests Implementing Model-Averaging Schemes in Detection of Rare Variants in Case-Control Studies.KNOWLEDGE DRIVEN BINNING AND PHEWAS ANALYSIS IN MARSHFIELD PERSONALIZED MEDICINE RESEARCH PROJECT USING BIOBINOpportunities and challenges of whole-genome and -exome sequencing.Region-based association tests for sequencing data on survival traits.Rare ADH variant constellations are specific for alcohol dependence.A biologically informed method for detecting rare variant associationsMeta-analysis methods for genome-wide association studies and beyond.Imputation of rare variants in next-generation association studies.Discovery of rare variants for complex phenotypes.Generalization of Rare Variant Association Tests for Longitudinal Family Studies.Genome-wide association analysis of imputed rare variants: application to seven common complex diseases.Human Genome Sequencing at the Population Scale: A Primer on High-Throughput DNA Sequencing and Analysis.On the substructure controls in rare variant analysis: Principal components or variance components?
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P2860
ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing data.
description
2012 nî lūn-bûn
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2012 թուականի Մարտին հրատարակուած գիտական յօդուած
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2012 թվականի մարտին հրատարակված գիտական հոդված
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2012年の論文
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2012年論文
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2012年論文
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2012年論文
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2012年論文
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2012年論文
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2012年论文
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name
ARIEL and AMELIA: testing for ...... xt-generation sequencing data.
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ARIEL and AMELIA: testing for ...... xt-generation sequencing data.
@en
ARIEL and AMELIA: testing for ...... xt-generation sequencing data.
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type
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ARIEL and AMELIA: testing for ...... xt-generation sequencing data.
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ARIEL and AMELIA: testing for ...... xt-generation sequencing data.
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ARIEL and AMELIA: testing for ...... xt-generation sequencing data.
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prefLabel
ARIEL and AMELIA: testing for ...... xt-generation sequencing data.
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ARIEL and AMELIA: testing for ...... xt-generation sequencing data.
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ARIEL and AMELIA: testing for ...... xt-generation sequencing data.
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P2860
P356
P1433
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ARIEL and AMELIA: testing for ...... xt-generation sequencing data.
@en
P2093
Aaron G Day-Williams
Andrew P Morris
P2860
P356
10.1159/000336982
P577
2012-03-22T00:00:00Z