Sequence kernel association tests for the combined effect of rare and common variants.
about
The MKK7 p.Glu116Lys Rare Variant Serves as a Predictor for Lung Cancer Risk and Prognosis in Chinese.Combining family- and population-based imputation data for association analysis of rare and common variants in large pedigreesProgress in methods for rare variant associationThe contribution of rare and common variants in 30 genes to risk nicotine dependenceIdentifying 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.Rare-Variant Kernel Machine Test for Longitudinal Data from Population and Family SamplesA W-test collapsing method for rare-variant association testing in exome sequencing data.Genes implicated in thiopurine-induced toxicity: Comparing TPMT enzyme activity with clinical phenotype and exome data in a paediatric IBD cohort.Powerful association test combining rare variant and gene expression using family data from Genetic Analysis Workshop 19.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 SamplesCommon coding variant in SERPINA1 increases the risk for large artery stroke.Robust and rapid algorithms facilitate large-scale whole genome sequencing downstream analysis in an integrative frameworkAmerindian-specific regions under positive selection harbour new lipid variants in Latinos.Kernel-machine testing coupled with a rank-truncation method for genetic pathway analysis.Detecting association of rare and common variants based on cross-validation prediction error.Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes.On the association analysis of genome-sequencing data: A spatial clustering approach for partitioning the entire genome into nonoverlapping windows.A powerful and adaptive association test for rare variantsCommon variation at PPARGC1A/B and change in body composition and metabolic traits following preventive interventions: the Diabetes Prevention ProgramGeneralized functional linear models for gene-based case-control association studiesQuantifying missing heritability at known GWAS loci.Greater power and computational efficiency for kernel-based association testing of sets of genetic variants.Dynamic Bayesian testing of sets of variants in complex diseases.Melanoma risk loci as determinants of melanoma recurrence and survivalIdentification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autismPlatelet count mediates the contribution of a genetic variant in LRRC16A to ARDS risk.A combination of targeted enrichment methodologies for whole-exome sequencing reveals novel pathogenic mutations.Pooled sequencing and rare variant association tests for identifying the determinants of emerging drug resistance in malaria parasitesContribution of large region joint associations to complex traits genetics.A robust GWSS method to simultaneously detect rare and common variants for complex disease.A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing.Exome analysis of patients with concurrent pediatric inflammatory bowel disease and autoimmune disease.Using Hamming Distance as Information for SNP-Sets Clustering and Testing in Disease Association Studies.Association of Genes, Pathways, and Haplogroups of the Mitochondrial Genome with the Risk of Colorectal Cancer: The Multiethnic Cohort.HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic SyndromeWeighted Score Tests Implementing Model-Averaging Schemes in Detection of Rare Variants in Case-Control Studies.Powerful Tests for Multi-Marker Association Analysis Using Ensemble Learning.Small Sample Kernel Association Tests for Human Genetic and Microbiome Association Studies
P2860
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P2860
Sequence kernel association tests for the combined effect of rare and common variants.
description
2013 nî lūn-bûn
@nan
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
2013年论文
@zh
2013年论文
@zh-cn
name
Sequence kernel association tests for the combined effect of rare and common variants.
@en
type
label
Sequence kernel association tests for the combined effect of rare and common variants.
@en
prefLabel
Sequence kernel association tests for the combined effect of rare and common variants.
@en
P2093
P2860
P1476
Sequence kernel association tests for the combined effect of rare and common variants.
@en
P2093
Seunggeun Lee
Vlad Makarov
Xihong Lin
P2860
P304
P356
10.1016/J.AJHG.2013.04.015
P407
P577
2013-05-16T00:00:00Z