Imputation of coding variants in African Americans: better performance using data from the exome sequencing project
about
Two-phase and family-based designs for next-generation sequencing studiesImputation of the rare HOXB13 G84E mutation and cancer risk in a large population-based cohortDISSCO: direct imputation of summary statistics allowing covariatesGuidelines for Large-Scale Sequence-Based Complex Trait Association Studies: Lessons Learned from the NHLBI Exome Sequencing Project.Whole-exome imputation of sequence variants identified two novel alleles associated with adult body height in African Americans.A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data.FISH: fast and accurate diploid genotype imputation via segmental hidden Markov model.Circadian CLOCK gene polymorphisms in relation to sleep patterns and obesity in African Americans: findings from the Jackson heart study.A population-specific reference panel empowers genetic studies of Anabaptist populations.Association studies with imputed variants using expectation-maximization likelihood-ratio tests.Rare variant association studies: considerations, challenges and opportunities.Gender-specific associations between ADIPOQ gene polymorphisms and adiponectin levels and obesity in the Jackson Heart Study cohortAssociation of ADIPOQ gene with type 2 diabetes and related phenotypes in African American men and women: the Jackson Heart StudyChoosing Subsamples for Sequencing Studies by Minimizing the Average Distance to the Closest LeafA multi-stage genome-wide association study of uterine fibroids in African AmericansVitamin D Receptor Gene Polymorphisms Are Associated with Abdominal Visceral Adipose Tissue Volume and Serum Adipokine Concentrations but Not with Body Mass Index or Waist Circumference in African Americans: The Jackson Heart Study.Evidence of selection as a cause for racial disparities in fibroproliferative disease.A powerful approach to test an optimally weighted combination of rare variants in admixed populations.Across-Platform Imputation of DNA Methylation Levels Incorporating Nonlocal Information Using Penalized Functional Regression.PreCimp: Pre-collapsing imputation approach increases imputation accuracy of rare variants in terms of collapsed variables.
P2860
Q26828744-442740DA-8592-4981-B89B-8868BD99DE9DQ28386845-2D2B7E9E-6F30-432F-8166-667597846CA4Q28646494-DB80B155-AD15-4DEC-9BEE-C5039D8A4133Q30275850-0158E046-1D28-4AD2-81AD-5FAB9885117FQ30362046-089DC839-A040-4B43-99C3-7F813C3D1716Q31034408-C3BDCBA4-732A-4FCB-86C3-6C0D46DCD202Q33807685-6529360B-3E04-4246-B897-5E7BE5335C9EQ33827514-3EE20A7F-1F27-41CE-B1F8-55D624552C62Q33921014-3740A0B5-97B5-4B27-9106-F75022517E49Q34482659-8636E06B-970A-4BAA-B906-54ADE22E74FFQ35110309-A6138016-878D-4611-9190-67C483968D61Q35750912-AAAFD8C9-3F8A-4DEC-8F21-9ABC47AC3503Q35877116-673AA87F-F722-407A-8DFA-4672F0797FF3Q36132246-27084D17-A956-4BEB-8DFF-BC364850B19AQ38610948-274D69A8-B734-4492-8915-70846DEED082Q39643783-8A3BA074-B782-4E5F-9361-8056AD3DB10BQ40089290-AF3525BD-31F4-475E-B3AE-B37582D60E7AQ41251024-10AC8BFE-4E17-4413-AB24-AC3EE3E45EBEQ41310707-8CE79CBF-688C-484C-BA05-4AD1A5B402A6Q50546663-D6E6B540-B47F-4B29-96E2-BC2EF4AF1D74
P2860
Imputation of coding variants in African Americans: better performance using data from the exome sequencing project
description
2013 nî lūn-bûn
@nan
2013 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Imputation of coding variants ...... m the exome sequencing project
@ast
Imputation of coding variants ...... m the exome sequencing project
@en
type
label
Imputation of coding variants ...... m the exome sequencing project
@ast
Imputation of coding variants ...... m the exome sequencing project
@en
prefLabel
Imputation of coding variants ...... m the exome sequencing project
@ast
Imputation of coding variants ...... m the exome sequencing project
@en
P2093
P2860
P50
P356
P1433
P1476
Imputation of coding variants ...... m the exome sequencing project
@en
P2093
Alex P Reiner
Chris Bizon
Chris S Carlson
Christina L Wassel
Deborah A Nickerson
Eric Yi Liu
Ethan M Lange
Gonçalo R Abecasis
Guosheng Zhang
Hyun Min Kang
P2860
P304
P356
10.1093/BIOINFORMATICS/BTT477
P407
P50
P577
2013-08-16T00:00:00Z