Association screening of common and rare genetic variants by penalized regression
about
In search of low-frequency and rare variants affecting complex traitsIntegration Analysis of Three Omics Data Using Penalized Regression Methods: An Application to Bladder CancerCircadian clock-related genetic risk scores and risk of placental abruptionRegularized Machine Learning in the Genetic Prediction of Complex TraitsRare variant association testing for next-generation sequencing data via hierarchical clustering.PUMA: a unified framework for penalized multiple regression analysis of GWAS dataGroup sparse canonical correlation analysis for genomic data integration.Regularized rare variant enrichment analysis for case-control exome sequencing data.A power set-based statistical selection procedure to locate susceptible rare variants associated with complex traits with sequencing data.Next Generation Statistical Genetics: Modeling, Penalization, and Optimization in High-Dimensional Data.Analysis of Genetic Analysis Workshop 18 data with gene-based penalized regression.Detecting rare variants for quantitative traits using nuclear families.Fast Genome-Wide QTL Association Mapping on Pedigree and Population Data.Genetic variation in the TP53 pathway and bladder cancer risk. a comprehensive analysis.The impact of rare and low-frequency genetic variants in common diseaseLongitudinal data analysis for rare variants detection with penalized quadratic inference functionA powerful and adaptive association test for rare variantsNext generation analytic tools for large scale genetic epidemiology studies of complex diseasesA 2-step penalized regression method for family-based next-generation sequencing association studies.Incorporating biological information into association studies of sequencing data.Enhancing the discovery of rare disease variants through hierarchical modelingPenalized-regression-based multimarker genotype analysis of Genetic Analysis Workshop 17 data.Evaluation of a LASSO regression approach on the unrelated samples of Genetic Analysis Workshop 17.Using LASSO regression to detect predictive aggregate effects in genetic studies.Penalized logistic regression for high-dimensional DNA methylation data with case-control studies.Mendel: the Swiss army knife of genetic analysis programs.Reconstructing DNA copy number by joint segmentation of multiple sequencesMultiple regression methods show great potential for rare variant association tests.A unified sparse representation for sequence variant identification for complex traits.Identification of rare causal variants in sequence-based studies: methods and applications to VPS13B, a gene involved in Cohen syndrome and autismPlacental genome and maternal-placental genetic interactions: a genome-wide and candidate gene association study of placental abruptionA novel support vector machine-based approach for rare variant detection.Fine-mapping additive and dominant SNP effects using group-LASSO and fractional resample model averaging.Pathways-driven sparse regression identifies pathways and genes associated with high-density lipoprotein cholesterol in two Asian cohortsMultivariate sparse group lasso for the multivariate multiple linear regression with an arbitrary group structureA scalable and portable framework for massively parallel variable selection in genetic association studies.Interactions of early adversity with stress-related gene polymorphisms impact regional brain structure in females.A FAST ALGORITHM FOR DETECTING GENE-GENE INTERACTIONS IN GENOME-WIDE ASSOCIATION STUDIESIdentifying rare and common variants with Bayesian variable selection.Fast identification of biological pathways associated with a quantitative trait using group lasso with overlaps
P2860
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P2860
Association screening of common and rare genetic variants by penalized regression
description
2010 nî lūn-bûn
@nan
2010 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Association screening of common and rare genetic variants by penalized regression
@ast
Association screening of common and rare genetic variants by penalized regression
@en
Association screening of common and rare genetic variants by penalized regression
@nl
type
label
Association screening of common and rare genetic variants by penalized regression
@ast
Association screening of common and rare genetic variants by penalized regression
@en
Association screening of common and rare genetic variants by penalized regression
@nl
prefLabel
Association screening of common and rare genetic variants by penalized regression
@ast
Association screening of common and rare genetic variants by penalized regression
@en
Association screening of common and rare genetic variants by penalized regression
@nl
P2093
P2860
P356
P1433
P1476
Association screening of common and rare genetic variants by penalized regression
@en
P2093
Janet S Sinsheimer
Kenneth Lange
Mary E Sehl
P2860
P304
P356
10.1093/BIOINFORMATICS/BTQ448
P407
P577
2010-08-06T00:00:00Z