相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy et al.
NATURE GENETICS (2016)
Next-generation genotype imputation service and methods
Sayantan Das et al.
NATURE GENETICS (2016)
The Rotterdam Study: 2016 objectives and design update
Albert Hofman et al.
EUROPEAN JOURNAL OF EPIDEMIOLOGY (2015)
A global reference for human genetic variation
David M. Altshuler et al.
NATURE (2015)
The UK10K project identifies rare variants in health and disease
Klaudia Walter et al.
NATURE (2015)
Assembling large genomes with single-molecule sequencing and locality-sensitive hashing
Konstantin Berlin et al.
NATURE BIOTECHNOLOGY (2015)
Population-specific genotype imputations using minimac or IMPUTE2
Elisabeth M. van Leeuwen et al.
NATURE PROTOCOLS (2015)
APPLICATIONS OF NEXT-GENERATION SEQUENCING Genetic variation and the de novo assembly of human genomes
Mark J. P. Chaisson et al.
NATURE REVIEWS GENETICS (2015)
Progress and promise in understanding the genetic basis of common diseases
Alkes L. Price et al.
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES (2015)
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
Jie Huang et al.
NATURE COMMUNICATIONS (2015)
The Genome of the Netherlands: design, and project goals
Dorret I. Boomsma et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2014)
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'
Patrick Deelen et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2014)
Whole-genome sequence variation, population structure and demographic history of the Dutch population
Laurent C. Francioli et al.
NATURE GENETICS (2014)
Quality control and conduct of genome-wide association meta-analyses
Thomas W. Winkler et al.
NATURE PROTOCOLS (2014)
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process
Henriet Springelkamp et al.
NATURE COMMUNICATIONS (2014)
Best Practices and Joint Calling of the HumanExome BeadChip: The CHARGE Consortium
Megan L. Grove et al.
PLOS ONE (2013)
An integrated map of genetic variation from 1,092 human genomes
David M. Altshuler et al.
NATURE (2012)
METAL: fast and efficient meta-analysis of genomewide association scans
Cristen J. Willer et al.
BIOINFORMATICS (2010)
ProbABEL package for genome-wide association analysis of imputed data
Yurii S. Aulchenko et al.
BMC BIOINFORMATICS (2010)
A map of human genome variation from population-scale sequencing
David Altshuler et al.
NATURE (2010)
Genotype imputation for genome-wide association studies
Jonathan Marchini et al.
NATURE REVIEWS GENETICS (2010)
The Path to Open-Angle Glaucoma Gene Discovery: Endophenotypic Status of Intraocular Pressure, Cup-to-Disc Ratio, and Central Corneal Thickness
Jac Charlesworth et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2010)
A Unified Approach to Genotype Imputation and Haplotype-Phase Inference for Large Data Sets of Trios and Unrelated Individuals
Brian L. Browning et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2009)
Genotype Imputation
Yun Li et al.
ANNUAL REVIEW OF GENOMICS AND HUMAN GENETICS (2009)
Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies
Ke Hao et al.
BMC GENETICS (2009)
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
Mark I. McCarthy et al.
NATURE REVIEWS GENETICS (2008)
GenABEL: an R library for genome-wide association analysis
Yurii S. Aulchenko et al.
BIOINFORMATICS (2007)
Linkage disequilibrium in young genetically isolated Dutch population
YS Aulchenko et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2004)