Comprehensive approach to analyzing rare genetic variants - Test2 - elhamkhani - TriplyDB

Comprehensive approach to analyzing rare genetic variants

Comprehensive approach to analyzing rare genetic variants

http://www.wikidata.org/entity/Q33745005

about

Insights into blood lipids from rare variant discovery Two-phase and family-based designs for next-generation sequencing studies Rare-variant association analysis: study designs and statistical tests Computational and statistical approaches to analyzing variants identified by exome sequencing Evaluation of logistic Bayesian LASSO for identifying association with rare haplotypes Strategies for Imputing and Analyzing Rare Variants in Association Studies A genetic signature of spina bifida risk from pathway-informed comprehensive gene-variant analysis Fine-scale patterns of population stratification confound rare variant association tests.Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease A variational Bayes discrete mixture test for rare variant association Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured data Regularized rare variant enrichment analysis for case-control exome sequencing data.A novel test for testing the optimally weighted combination of rare and common variants based on data of parents and affected children.Testing genetic association with rare and common variants in family data.Identifying rare and common disease associated variants in genomic data using Parkinson's disease as a model.Performance of statistical methods on CHARGE targeted sequencing data Rare variants analysis using penalization methods for whole genome sequence data.The impact of rare and low-frequency genetic variants in common disease Incorporating prior biologic information for high-dimensional rare variant association studies 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.A powerful and adaptive association test for rare variants A rare variant association test based on combinations of single-variant tests.Next generation analytic tools for large scale genetic epidemiology studies of complex diseases The power comparison of the haplotype-based collapsing tests and the variant-based collapsing tests for detecting rare variants in pedigrees.TARV: tree-based analysis of rare variants identifying risk modifying variants in CTNNA2 and CNTNAP2 for alcohol addiction.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 variants Comparison of statistical approaches to rare variant analysis for quantitative traits.Use of principal components to aggregate rare variants in case-control and family-based association studies in the presence of multiple covariates Incorporating gene-environment interaction in testing for association with rare genetic variants Predicting signatures of "synthetic associations" and "natural associations" from empirical patterns of human genetic variation.Cohen's h for detection of disease association with rare genetic variants.Multiple regression methods show great potential for rare variant association tests.Rare variant analysis for family-based design.Joint analysis for integrating two related studies of different data types and different study designs using hierarchical modeling approaches.Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.Population genetic simulations of complex phenotypes with implications for rare variant association tests Leveraging prior information to detect causal variants via multi-variant regression.BioBin: a bioinformatics tool for automating the binning of rare variants using publicly available biological knowledge.

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Comprehensive approach to analyzing rare genetic variants

http://www.wikidata.org/entity/Q33745005

description

2010 nî lūn-bûn

@nan

2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի նոյեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Comprehensive approach to analyzing rare genetic variants

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Comprehensive approach to analyzing rare genetic variants

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Comprehensive approach to analyzing rare genetic variants

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Comprehensive approach to analyzing rare genetic variants

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prefLabel

Comprehensive approach to analyzing rare genetic variants

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Comprehensive approach to analyzing rare genetic variants

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Comprehensive approach to analyzing rare genetic variants

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John S Witte

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Nicholas J Marini

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Thomas J Hoffmann

http://www.w3.org/2001/XMLSchema#string

P2860

Multiple Rare Alleles Contribute to Low Plasma Levels of HDL Cholesterol

The allelic structure of common disease

Are rare variants responsible for susceptibility to complex diseases?

Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes

The impact of next-generation sequencing technology on genetics

Coding sequence rare variants identified in MYBPC3, MYH6, TPM1, TNNC1, and TNNI3 from 312 patients with familial or idiopathic dilated cardiomyopathy

Pooled association tests for rare variants in exon-resequencing studies

SIFT: Predicting amino acid changes that affect protein function

Human non-synonymous SNPs: server and survey

Rare variants create synthetic genome-wide associations

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scholarly article

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10.1371/JOURNAL.PONE.0013584

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21072163

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2972202

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