Finding unique filter sets in PLATO: a precursor to efficient interaction analysis in GWAS data.
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Replication and characterisation of genetic variants in the fibrinogen gene cluster with plasma fibrinogen levels and haematological traits in the Third National Health and Nutrition Examination SurveyPopulation Stratification in the Context of Diverse Epidemiologic Surveys Sans Genome-Wide DataAnalysis pipeline for the epistasis search - statistical versus biological filtering.Environment-wide association study (EWAS) for type 2 diabetes in the Marshfield Personalized Medicine Research Project BiobankPhenome-Wide Association Studies as a Tool to Advance Precision Medicine.A single nucleotide polymorphism in SLC7A5 is associated with gastrointestinal toxicity after high-dose melphalan and autologous stem cell transplantation for multiple myelomaGenetic variation in iron metabolism is associated with neuropathic pain and pain severity in HIV-infected patients on antiretroviral therapy.Characterization of genome-wide association-identified variants for atrial fibrillation in African Americans.Quality control procedures for genome-wide association studies.Use of biological knowledge to inform the analysis of gene-gene interactions involved in modulating virologic failure with efavirenz-containing treatment regimens in ART-naïve ACTG clinical trials participants.Identification of gene-gene and gene-environment interactions within the fibrinogen gene cluster for fibrinogen levels in three ethnically diverse populations.Statistical Optimization of Pharmacogenomics Association Studies: Key Considerations from Study Design to AnalysisVariants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studiesMitochondrial genomics and CD4 T-cell count recovery after antiretroviral therapy initiation in AIDS clinical trials group study 384Cost-effective prediction of gender-labeling errors and estimation of gender-labeling error rates in candidate-gene association studies.Fine mapping study reveals novel candidate genes for carotid intima-media thickness in Dominican Republican familiesPredicting warfarin dosage in European-Americans and African-Americans using DNA samples linked to an electronic health record.Biology-Driven Gene-Gene Interaction Analysis of Age-Related Cataract in the eMERGE Network.Sequencing of candidate genes in Dominican families implicates both rare exonic and common non-exonic variants for carotid intima-media thickness at bifurcation.Rare Variants in NOD1 Associated with Carotid Bifurcation Intima-Media Thickness in Dominican Republic Families.Genome-wide study of resistant hypertension identified from electronic health records.BIOFILTER AS A FUNCTIONAL ANNOTATION PIPELINE FOR COMMON AND RARE COPY NUMBER BURDENEvaluating mitochondrial DNA variation in autism spectrum disorders.Characterization of the Metabochip in diverse populations from the International HapMap Project in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) projectMitochondrial DNA variation and HIV-associated sensory neuropathy in CHARTER.Next-generation analysis of cataracts: determining knowledge driven gene-gene interactions using Biofilter, and gene-environment interactions using the PhenX Toolkit.Predicting clopidogrel response using DNA samples linked to an electronic health record.Assessment of a pharmacogenomic marker panel in a polypharmacy population identified from electronic medical recordsGeneralization of variants identified by genome-wide association studies for electrocardiographic traits in African AmericansTowards precision medicine: advances in computational approaches for the analysis of human variantsMulti-locus candidate gene analyses of lipid levels in a pediatric Turkish cohort: lessons learned on LPL, CETP, LIPC, ABCA1, and SHBGUtilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients.SEXCMD: Development and validation of sex marker sequences for whole-exome/genome and RNA sequencing.Epiregulin (EREG) and human V-ATPase (TCIRG1): genetic variation, ethnicity and pulmonary tuberculosis susceptibility in Guinea-Bissau and The Gambia.Evaluation of PrediXcan for prioritizing GWAS associations and predicting gene expression.Sequencing of Linkage Region on Chromosome 12p11 Identifies PKP2 as a Candidate Gene for Left Ventricular Mass in Dominican Families.Replication of Associations with Electrocardio-graphic Traits in African Americans from Clinical and Epidemiologic Studies
P2860
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P2860
Finding unique filter sets in PLATO: a precursor to efficient interaction analysis in GWAS data.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին 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
Finding unique filter sets in ...... raction analysis in GWAS data.
@ast
Finding unique filter sets in ...... raction analysis in GWAS data.
@en
Finding unique filter sets in ...... raction analysis in GWAS data.
@nl
type
label
Finding unique filter sets in ...... raction analysis in GWAS data.
@ast
Finding unique filter sets in ...... raction analysis in GWAS data.
@en
Finding unique filter sets in ...... raction analysis in GWAS data.
@nl
prefLabel
Finding unique filter sets in ...... raction analysis in GWAS data.
@ast
Finding unique filter sets in ...... raction analysis in GWAS data.
@en
Finding unique filter sets in ...... raction analysis in GWAS data.
@nl
P2093
P2860
P1476
Finding unique filter sets in ...... raction analysis in GWAS data.
@en
P2093
Benjamin J Grady
David Sexton
Eric Torstenson
Justin Giles
Scott M Dudek
P2860
P304
P577
2010-01-01T00:00:00Z