about
Human genetics and genomics a decade after the release of the draft sequence of the human genomeGenome-wide association studies of chronic kidney disease: what have we learned?Computational and statistical approaches to analyzing variants identified by exome sequencingCopper phenotype in Alzheimer's disease: dissecting the pathwayIntegration and Fixation Preferences of Human and Mouse Endogenous Retroviruses Uncovered with Functional Data AnalysisWeighted pedigree-based statistics for testing the association of rare variantsMultiscale integration of -omic, imaging, and clinical data in biomedical informatics.Methods for collapsing multiple rare variants in whole-genome sequence data.Region-Based Association Test for Familial Data under Functional Linear ModelsAn Empirical Bayes risk prediction model using multiple traits for sequencing data.A new statistical framework for genetic pleiotropic analysis of high dimensional phenotype data.Epistasis analysis for quantitative traits by functional regression model.Longitudinal data analysis for rare variants detection with penalized quadratic inference functionLongitudinal analysis is more powerful than cross-sectional analysis in detecting genetic association with neuroimaging phenotypes.A powerful and adaptive association test for rare variantsA comparison of two collapsing methods in different approaches.Comparison of several sequence-based association methods in pedigreesTARV: tree-based analysis of rare variants identifying risk modifying variants in CTNNA2 and CNTNAP2 for alcohol addiction.Functional linear models for association analysis of quantitative traits.A comprehensive evaluation of collapsing methods using simulated and real data: excellent annotation of functionality and large sample sizes required.Functional logistic regression approach to detecting gene by longitudinal environmental exposure interaction in a case-control study.Generalized functional linear models for gene-based case-control association studiesMultiple regression methods show great potential for rare variant association tests.Pool-hmm: a Python program for estimating the allele frequency spectrum and detecting selective sweeps from next generation sequencing of pooled samples.Properties and modeling of GWAS when complex disease risk is due to non-complementing, deleterious mutations in genes of large effect.Identifying Mendelian disease genes with the variant effect scoring toolRe-ranking sequencing variants in the post-GWAS era for accurate causal variant identificationParadigm shift in treatment of Alzheimer's disease: zinc therapy now a conscientious choice for care of individual patients.On family-based genome-wide association studies with large pedigrees: observations and recommendations.Powerful Tukey's One Degree-of-Freedom Test for Detecting Gene-Gene and Gene-Environment InteractionsNGS technologies for analyzing germplasm diversity in genebanks.Analysis of mixtures using next generation sequencing of mitochondrial DNA hypervariable regions.Family-based association studies for next-generation sequencing.Gene-Based Association Analysis for Censored Traits Via Fixed Effect Functional Regressions.Quantitative trait locus analysis for next-generation sequencing with the functional linear models.Smoothed functional principal component analysis for testing association of the entire allelic spectrum of genetic variationMeta-analysis of Complex Diseases at Gene Level with Generalized Functional Linear ModelsUncovering Local Trends in Genetic Effects of Multiple Phenotypes via Functional Linear Models.Genotype to phenotype via network analysis.The Moroccan Genetic Disease Database (MGDD): a database for DNA variations related to inherited disorders and disease susceptibility.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Association studies for next-generation sequencing.
@ast
Association studies for next-generation sequencing.
@en
type
label
Association studies for next-generation sequencing.
@ast
Association studies for next-generation sequencing.
@en
prefLabel
Association studies for next-generation sequencing.
@ast
Association studies for next-generation sequencing.
@en
P2860
P356
P1433
P1476
Association studies for next-generation sequencing.
@en
P2093
P2860
P304
P356
10.1101/GR.115998.110
P577
2011-04-26T00:00:00Z