Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.
about
Massively parallel sequencing: the new frontier of hematologic genomicsRare-variant association analysis: study designs and statistical testsStrategies for Imputing and Analyzing Rare Variants in Association StudiesImputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohortDISSCO: direct imputation of summary statistics allowing covariatesGenome-wide scan of 29,141 African Americans finds no evidence of directional selection since admixtureGuidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project.Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits.Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.Impact of genetic variation on three dimensional structure and function of proteins.A variational Bayes discrete mixture test for rare variant associationImputation of coding variants in African Americans: better performance using data from the exome sequencing projectEffective filtering strategies to improve data quality from population-based whole exome sequencing studies.Integrative analysis of sequencing and array genotype data for discovering disease associations with rare mutations.Likelihood-based complex trait association testing for arbitrary depth sequencing data.A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data.The genetics of platelet count and volume in humans.Common coding variant in SERPINA1 increases the risk for large artery stroke.Hematopoietic progenitor cell mobilization is more robust in healthy African American compared to Caucasian donors and is not affected by the presence of sickle cell traitLarge multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African AmericansSequencing and de novo assembly of 150 genomes from Denmark as a population referenceAssociation studies with imputed variants using expectation-maximization likelihood-ratio tests.Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studies.Rare variant association studies: considerations, challenges and opportunities.Design of DNA pooling to allow incorporation of covariates in rare variants analysisGenetics of allergic diseases.Defining "mutation" and "polymorphism" in the era of personal genomics.One Size Doesn't Fit All - RefEditor: Building Personalized Diploid Reference Genome to Improve Read Mapping and Genotype Calling in Next Generation Sequencing Studies.Sickle cell trait diagnosis: clinical and social implications.Group association test using a hidden Markov model.From GWAS to function: lessons from blood cells.Genome-wide association study of age at menarche in African-American women.Applications of high-throughput DNA sequencing to benign hematologyiCAGES: integrated CAncer GEnome Score for comprehensively prioritizing driver genes in personal cancer genomes.Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps.Hydroxycarbamine: from an Old Drug Used in Malignant Hemopathies to a Current Standard in Sickle Cell Disease.
P2860
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P2860
Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing Project.
description
2012 nî lūn-bûn
@nan
2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Imputation of exome sequence v ...... I GO Exome Sequencing Project.
@ast
Imputation of exome sequence v ...... I GO Exome Sequencing Project.
@en
type
label
Imputation of exome sequence v ...... I GO Exome Sequencing Project.
@ast
Imputation of exome sequence v ...... I GO Exome Sequencing Project.
@en
prefLabel
Imputation of exome sequence v ...... I GO Exome Sequencing Project.
@ast
Imputation of exome sequence v ...... I GO Exome Sequencing Project.
@en
P2093
P2860
P1476
Imputation of exome sequence v ...... BI GO Exome Sequencing Project
@en
P2093
Alex P Reiner
Andrew D Johnson
Benjamin A Logsdon
Christopher J O'Donnell
Ethan M Lange
Guillaume Lettre
Guosheng Zhang
James G Wilson
Jill M Johnsen
P2860
P304
P356
10.1016/J.AJHG.2012.08.031
P407
P577
2012-10-25T00:00:00Z