Trimming, weighting, and grouping SNPs in human case-control association studies.
about
Multilocus genetic analysis of brain imagesGenetics of the connectomePLINK: a tool set for whole-genome association and population-based linkage analysesMultiple ADH genes modulate risk for drug dependence in both African- and European-AmericansStatistical significance for hierarchical clustering in genetic association and microarray expression studiesADH4 gene variation is associated with alcohol dependence and drug dependence in European Americans: results from HWD tests and case-control association studiesAlzheimer disease pathology in cognitively healthy elderly: a genome-wide studyFucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's diseaseMultivariate genomewide linkage scan of neurocognitive traits and ADHD symptoms: suggestive linkage to 3q13.Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memoryAn approach to predict the risk of glaucoma development by integrating different attribute data.Multilocus statistics to uncover epistasis and heterogeneity in complex diseases: revisiting a set of multiple sclerosis data.Genetic polymorphisms in the nucleotide excision repair pathway and lung cancer risk: a meta-analysis.Analysis of baseline, average, and longitudinally measured blood pressure data using linear mixed modelsEfficient computation of significance levels for multiple associations in large studies of correlated data, including genomewide association studies.Selection of single-nucleotide polymorphisms in disease association data.A forest-based feature screening approach for large-scale genome data with complex structures.Dissecting trait heterogeneity: a comparison of three clustering methods applied to genotypic dataTesting groups of genomic locations for enrichment in disease loci using linkage scan data: a method for hypothesis testing.Linking brain imaging and genomics in the study of Alzheimer's disease and aging.Rationale and study design of the CardioGene Study: genomics of in-stent restenosis.Evaluation of genome-wide power of genetic association studies based on empirical data from the HapMap project.Resampling-based multiple comparison procedure with application to point-wise testing with functional data.Detecting susceptibility genes in case-control studies using set associationMultifactor-dimensionality reduction versus family-based association tests in detecting susceptibility loci in discordant sib-pair studies.The challenge for genetic epidemiologists: how to analyze large numbers of SNPs in relation to complex diseases.Detection of gene x gene interactions in genome-wide association studies of human population data.Association between common variation in 120 candidate genes and breast cancer risk.Alternative contingency table measures improve the power and detection of multifactor dimensionality reductionTesting gene set enrichment for subset of genes: Sub-GSE.A random forest approach to the detection of epistatic interactions in case-control studies.Detecting disease-associated genotype patternsEpistatic module detection for case-control studies: a Bayesian model with a Gibbs sampling strategy.Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancerRegression-based approach for testing the association between multi-region haplotype configuration and complex trait.Detecting purely epistatic multi-locus interactions by an omnibus permutation test on ensembles of two-locus analyses.Simultaneous analysis of all single-nucleotide polymorphisms in genome-wide association study of rheumatoid arthritis.An omnibus permutation test on ensembles of two-locus analyses can detect pure epistasis and genetic heterogeneity in genome-wide association studies.Antioxidant defense enzyme genes and asthma susceptibility: gender-specific effects and heterogeneity in gene-gene interactions between pathogenetic variants of the diseaseProbability theory-based SNP association study method for identifying susceptibility loci and genetic disease models in human case-control data.
P2860
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P2860
Trimming, weighting, and grouping SNPs in human case-control association studies.
description
2001 nî lūn-bûn
@nan
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
2001年學術文章
@zh
2001年學術文章
@zh-hant
name
Trimming, weighting, and grouping SNPs in human case-control association studies.
@en
type
label
Trimming, weighting, and grouping SNPs in human case-control association studies.
@en
prefLabel
Trimming, weighting, and grouping SNPs in human case-control association studies.
@en
P2093
P2860
P356
P1433
P1476
Trimming, weighting, and grouping SNPs in human case-control association studies.
@en
P2093
P2860
P304
P356
10.1101/GR.204001
P577
2001-12-01T00:00:00Z