Related references
Note: Only part of the references are listed.The genetic history of France
Aude Saint Pierre et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2020)
Fast and accurate relatedness estimation from high-throughput sequencing data in the presence of inbreeding
Kristian Hanghoj et al.
GIGASCIENCE (2019)
Allele balance bias identifies systematic genotyping errors and false disease associations
Francesc Muyas et al.
HUMAN MUTATION (2019)
Whole-Exome Sequencing in the Isolated Populations of Cilento from South Italy
T. Nutile et al.
SCIENTIFIC REPORTS (2019)
Strategies for phasing and imputation in a population isolate
Anthony Francis Herzig et al.
GENETIC EPIDEMIOLOGY (2018)
How to estimate kinship
Jerome Goudet et al.
MOLECULAR ECOLOGY (2018)
Detecting the dominance component of heritability in isolated and outbred human populations
Anthony F. Herzig et al.
SCIENTIFIC REPORTS (2018)
Orthogonal Estimates of Variances for Additive, Dominance, and Epistatic Effects in Populations
Zulma G. Vitezica et al.
GENETICS (2017)
Estimation of kinship coefficient in structured and admixed populations using sparse sequencing data
Jinzhuang Dou et al.
PLOS GENETICS (2017)
Orthogonal Estimates of Variances for Additive, Dominance, and Epistatic Effects in Populations
Zulma G. Vitezica et al.
GENETICS (2017)
Genotype Imputation with Millions of Reference Samples
Brian L. Browning et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
Very low-depth sequencing in a founder population identifies a cardioprotective APOC3 signal missed by genome-wide imputation
Arthur Gilly et al.
HUMAN MOLECULAR GENETICS (2016)
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy et al.
NATURE GENETICS (2016)
Strategies for determining kinship in wild populations using genetic data
Veronika Staedele et al.
ECOLOGY AND EVOLUTION (2016)
Dominance Genetic Variation Contributes Little to the Missing Heritability for Human Complex Traits
Zhihong Zhu et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2015)
Sambamba: fast processing of NGS alignment formats
Artem Tarasov et al.
BIOINFORMATICS (2015)
Sparse whole-genome sequencing identifies two loci for major depressive disorder
Na Cai et al.
NATURE (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)
The future of ancient DNA: Technical advances and conceptual shifts
Michael Hofreiter et al.
BIOESSAYS (2015)
Relatedness in the post-genomic era: is it still useful?
Doug Speed et al.
NATURE REVIEWS GENETICS (2015)
Toward better understanding of artifacts in variant calling from high-coverage samples
Heng Li
BIOINFORMATICS (2014)
ANGSD: Analysis of Next Generation Sequencing Data
Thorfinn Sand Korneliussen et al.
BMC BIOINFORMATICS (2014)
Sequencing depth and coverage: key considerations in genomic analyses
David Sims et al.
NATURE REVIEWS GENETICS (2014)
Identity by Descent: Variation in Meiosis, Across Genomes, and in Populations
Elizabeth A. Thompson
GENETICS (2013)
Estimating inbreeding coefficients from NGS data: Impact on genotype calling and allele frequency estimation
Filipe G. Vieira et al.
GENOME RESEARCH (2013)
GCTA: A Tool for Genome-wide Complex Trait Analysis
Jian Yang et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2011)
Estimation of allele frequency and association mapping using next-generation sequencing data
Su Yeon Kim et al.
BMC BIOINFORMATICS (2011)
A framework for variation discovery and genotyping using next-generation DNA sequencing data
Mark A. DePristo et al.
NATURE GENETICS (2011)
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
Aaron McKenna et al.
GENOME RESEARCH (2010)
Common SNPs explain a large proportion of the heritability for human height
Jian Yang et al.
NATURE GENETICS (2010)
New approaches to population stratification in genome-wide association studies
Alkes L. Price et al.
NATURE REVIEWS GENETICS (2010)
The Sequence Alignment/Map format and SAMtools
Heng Li et al.
BIOINFORMATICS (2009)
Comparing population structure as inferred from genealogical versus genetic information
Vincenza Colonna et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2009)
Efficient Methods to Compute Genomic Predictions
P. M. VanRaden
JOURNAL OF DAIRY SCIENCE (2008)
Genes mirror geography within Europe
John Novembre et al.
NATURE (2008)
Campora: A young genetic isolate in South Italy
Vincenza Colonna et al.
HUMAN HEREDITY (2007)
Multipoint linkage analysis with many multiallelic or dense diallelic markers: Markov chain-Monte Carlo provides practical approaches for genome scans on general pedigrees
Ellen M. Wijsman et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Genetic relatedness analysis: modern data and new challenges
Bruce S. Weir et al.
NATURE REVIEWS GENETICS (2006)
Principal components analysis corrects for stratification in genome-wide association studies
Alkes L. Price et al.
NATURE GENETICS (2006)