Analysis of multiple SNPs in a candidate gene or region.
about
Inherited variation in immune genes and pathways and glioblastoma riskIntroduction to deep sequencing and its application to drug addiction research with a focus on rare variants.Studying gene and gene-environment effects of uncommon and common variants on continuous traits: a marker-set approach using gene-trait similarity regression.Identifying rare and common disease associated variants in genomic data using Parkinson's disease as a model.Comparison of methods for competitive tests of pathway analysisRare-Variant Kernel Machine Test for Longitudinal Data from Population and Family SamplesImproving power in genetic-association studies via wavelet transformation.A data-adaptive sum test for disease association with multiple common or rare variants.A novel adaptive method for the analysis of next-generation sequencing data to detect complex trait associations with rare variants due to gene main effects and interactions.Genome-wide investigation of regional blood-based DNA methylation adjusted for complete blood counts implicates BNC2 in ovarian cancer.From SNPs to genes: disease association at the gene levelGene-based tests of associationGenome-wide association studies for discrete traitsGene set analysis of GWAS data for human longevity highlights the relevance of the insulin/IGF-1 signaling and telomere maintenance pathways.On the Aggregation of Multimarker Information for Marker-Set and Sequencing Data Analysis: Genotype Collapsing vs. Similarity Collapsing.Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variantsTesting SNPs and sets of SNPs for importance in association studies.Evolutionary adaptation of the amino acid and codon usage of the mosquito sodium channel following insecticide selection in the field mosquitoes.Hierarchical Naive Bayes for genetic association studiesA method for gene-based pathway analysis using genomewide association study summary statistics reveals nine new type 1 diabetes associations.Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.Identifying disease associated genes by network propagation.Comparisons of multi-marker association methods to detect association between a candidate region and disease.Associations between paternally transmitted fetal IGF2 variants and maternal circulating glucose concentrations in pregnancy.Using the gene ontology to scan multilevel gene sets for associations in genome wide association studiesA powerful test for multiple rare variants association studies that incorporates sequencing qualities.Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjectsRare Variants Association Analysis in Large-Scale Sequencing Studies at the Single Locus LevelPermutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis.Genetic variants associated with the risk of chronic obstructive pulmonary disease with and without lung cancer.Multiple mutations and mutation combinations in the sodium channel of permethrin resistant mosquitoes, Culex quinquefasciatus.CEDER: accurate detection of differentially expressed genes by combining significance of exons using RNA-Seq.Multiple SNP Set Analysis for Genome-Wide Association Studies Through Bayesian Latent Variable Selection.Statistical tests for detecting associations with groups of genetic variants: generalization, evaluation, and implementation.Kernel machine SNP-set testing under multiple candidate kernels.On multi-marker tests for association in case-control studies.Hypothesis-driven candidate gene association studies: practical design and analytical considerations.Multiple linear combination (MLC) regression tests for common variants adapted to linkage disequilibrium structureComparison of statistical tests for disease association with rare variants.Adaptive tests for detecting gene-gene and gene-environment interactions
P2860
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P2860
Analysis of multiple SNPs in a candidate gene or region.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh
2008年學術文章
@zh-hant
name
Analysis of multiple SNPs in a candidate gene or region.
@en
type
label
Analysis of multiple SNPs in a candidate gene or region.
@en
prefLabel
Analysis of multiple SNPs in a candidate gene or region.
@en
P2860
P356
P1433
P1476
Analysis of multiple SNPs in a candidate gene or region.
@en
P2093
Juliet Chapman
P2860
P304
P356
10.1002/GEPI.20330
P577
2008-09-01T00:00:00Z