Related references
Note: Only part of the references are listed.The APOBEC3 genes and their role in cancer: insights from human papillomavirus
Nicola J. Smith et al.
JOURNAL OF MOLECULAR ENDOCRINOLOGY (2019)
Characterizing the Major Structural Variant Alleles of the Human Genome
Peter A. Audano et al.
CELL (2019)
Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity
Bradley P. Coe et al.
NATURE GENETICS (2019)
Long-read sequence and assembly of segmental duplications
Mitchell R. Vollger et al.
NATURE METHODS (2019)
An upstream protein-coding region in enteroviruses modulates virus infection in gut epithelial cells
Valeria Lulla et al.
NATURE MICROBIOLOGY (2019)
Physiological and Genetic Adaptations to Diving in Sea Nomads
Melissa A. Ilardo et al.
CELL (2018)
High-resolution comparative analysis of great ape genomes
Zev N. Kronenberg et al.
SCIENCE (2018)
Evolution and cell-type specificity of human-specific genes preferentially expressed in progenitors of fetal neocortex
Marta Florio et al.
ELIFE (2018)
Transcriptional fates of human-specific segmental duplications in brain
Max L. Dougherty et al.
GENOME RESEARCH (2018)
Archaic Adaptive Introgression in TBX15/WARS2
Fernando Racimo et al.
MOLECULAR BIOLOGY AND EVOLUTION (2017)
A Neolithic expansion, but strong genetic structure, in the independent history of New Guinea
Anders Bergstrom et al.
SCIENCE (2017)
A high-coverage Neandertal genome from Vindija Cave in Croatia
Kay Pruefer et al.
SCIENCE (2017)
Deactivating Fatty Acids: Acyl-CoA Thioesterase-Mediated Control of Lipid Metabolism
Veronika Tillander et al.
TRENDS IN ENDOCRINOLOGY AND METABOLISM (2017)
Computationally Efficient Composite Likelihood Statistics for Demographic Inference
Alec J. Coffman et al.
MOLECULAR BIOLOGY AND EVOLUTION (2016)
The mutation rate in human evolution and demographic inference
Aylwyn Scally
CURRENT OPINION IN GENETICS & DEVELOPMENT (2016)
Interchromosomal core duplicons drive both evolutionary instability and disease susceptibility of the Chromosome 8p23.1 region
Kiana Mohajeri et al.
GENOME RESEARCH (2016)
Whole-genome sequence analyses of Western Central African Pygmy hunter-gatherers reveal a complex demographic history and identify candidate genes under positive natural selection
PingHsun Hsieh et al.
GENOME RESEARCH (2016)
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility
Xander Nuttle et al.
NATURE (2016)
A genomic history of Aboriginal Australia
Anna-Sapfo Malaspinas et al.
NATURE (2016)
Genomic insights into the peopling of the Southwest Pacific
Pontus Skoglund et al.
NATURE (2016)
The Simons Genome Diversity Project: 300 genomes from 142 diverse populations
Swapan Mallick et al.
NATURE (2016)
Excavating Neandertal and Denisovan DNA from the genomes of Melanesian individuals
Benjamin Vernot et al.
SCIENCE (2016)
DEFA gene variants associated with IgA nephropathy in a Chinese population
Y. Y. Qi et al.
GENES AND IMMUNITY (2015)
An integrated map of structural variation in 2,504 human genomes
Peter H. Sudmant et al.
NATURE (2015)
Large multiallelic copy number variations in humans
Robert E. Handsaker et al.
NATURE GENETICS (2015)
Greenlandic Inuit show genetic signatures of diet and climate adaptation
Matteo Fumagalli et al.
SCIENCE (2015)
Global diversity, population stratification, and selection of human copy-number variation
Peter H. Sudmant et al.
SCIENCE (2015)
Wham: Identifying Structural Variants of Biological Consequence
Zev N. Kronenberg et al.
PLOS COMPUTATIONAL BIOLOGY (2015)
The complete genome sequence of a Neanderthal from the Altai Mountains
Kay Pruefer et al.
NATURE (2014)
Altitude adaptation in Tibetans caused by introgression of Denisovan-like DNA
Emilia Huerta-Sanchez et al.
NATURE (2014)
BEAST 2: A Software Platform for Bayesian Evolutionary Analysis
Remco Bouckaert et al.
PLOS COMPUTATIONAL BIOLOGY (2014)
LUMPY: a probabilistic framework for structural variant discovery
Ryan M. Layer et al.
GENOME BIOLOGY (2014)
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
Kazutaka Katoh et al.
MOLECULAR BIOLOGY AND EVOLUTION (2013)
Great ape genetic diversity and population history
Javier Prado-Martinez et al.
NATURE (2013)
A Haplotype at STAT2 Introgressed from Neanderthals and Serves as a Candidate of Positive Selection in Papua New Guinea
Fernando L. Mendez et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2012)
DELLY: structural variant discovery by integrated paired-end and split-read analysis
Tobias Rausch et al.
BIOINFORMATICS (2012)
Insights into hominid evolution from the gorilla genome sequence
Aylwyn Scally et al.
NATURE (2012)
Structural diversity and African origin of the 17q21.31 inversion polymorphism
Karyn Meltz Steinberg et al.
NATURE GENETICS (2012)
Generation times in wild chimpanzees and gorillas suggest earlier divergence times in great ape and human evolution
Kevin E. Langergraber et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2012)
A High-Coverage Genome Sequence from an Archaic Denisovan Individual
Matthias Meyer et al.
SCIENCE (2012)
A Worldwide Analysis of Beta-Defensin Copy Number Variation Suggests Recent Selection of a High-Expressing DEFB103 Gene Copy in East Asia
Robert J. Hardwick et al.
HUMAN MUTATION (2011)
Origins and functional impact of copy number variation in the human genome
Donald F. Conrad et al.
NATURE (2010)
Genetic history of an archaic hominin group from Denisova Cave in Siberia
David Reich et al.
NATURE (2010)
A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk
Francesca Antonacci et al.
NATURE GENETICS (2010)
mrsFAST: a cache-oblivious algorithm for short-read mapping
Faraz Hach et al.
NATURE METHODS (2010)
Diversity of Human Copy Number Variation and Multicopy Genes
Peter H. Sudmant et al.
SCIENCE (2010)
Sequencing of 50 Human Exomes Reveals Adaptation to High Altitude
Xin Yi et al.
SCIENCE (2010)
Fast and flexible simulation of DNA sequence data
Gary K. Chen et al.
GENOME RESEARCH (2009)
Fast model-based estimation of ancestry in unrelated individuals
David H. Alexander et al.
GENOME RESEARCH (2009)
Characterization of six human disease-associated inversion polymorphisms
Francesca Antonacci et al.
HUMAN MOLECULAR GENETICS (2009)
APOBEC3B Deletion and Risk of HIV-1 Acquisition
Ping An et al.
JOURNAL OF INFECTIOUS DISEASES (2009)
Inferring the Joint Demographic History of Multiple Populations from Multidimensional SNP Frequency Data
Ryan N. Gutenkunst et al.
PLOS GENETICS (2009)
Adaptive evolution of UGT2B17 copy-number variation
Yali Xue et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Association between microdeletion and microduplication at 16p11.2 and autism
Lauren A. Weiss et al.
NEW ENGLAND JOURNAL OF MEDICINE (2008)
Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering
Sharon R. Browning et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
A second generation human haplotype map of over 3.1 million SNPs
Kelly A. Frazer et al.
NATURE (2007)
Diet and the evolution of human amylase gene copy number variation
George H. Perry et al.
NATURE GENETICS (2007)
PAML 4: Phylogenetic analysis by maximum likelihood
Ziheng Yang
MOLECULAR BIOLOGY AND EVOLUTION (2007)
MEGA4: Molecular evolutionary genetics analysis (MEGA) software version 4.0
Koichiro Tamura et al.
MOLECULAR BIOLOGY AND EVOLUTION (2007)
Population stratification of a common APOBEC gene deletion polymorphism
Jeffrey M. Kidd et al.
PLOS GENETICS (2007)
Convergent adaptation of human lactase persistence in Africa and Europe
Sarah A. Tishkoff et al.
NATURE GENETICS (2007)
Global variation in copy number in the human genome
Richard Redon et al.
NATURE (2006)
RAxML-VI-HPC: Maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
Alexandros Stamatakis
BIOINFORMATICS (2006)
Widespread discordance of gene trees with species tree in Drosophila:: Evidence for incomplete lineage sorting
Daniel A. Pollard et al.
PLOS GENETICS (2006)
PAL2NAL: robust conversion of protein sequence alignments into the corresponding codon alignments
Mikita Suyama et al.
NUCLEIC ACIDS RESEARCH (2006)
Possible ancestral structure in human populations
Vincent Plagnol et al.
PLOS GENETICS (2006)
A common inversion under selection in Europeans
H Stefansson et al.
NATURE GENETICS (2005)
Detecting recent positive selection in the human genome from haplotype structure
PC Sabeti et al.
NATURE (2002)
Positive selection of a gene family during the emergence of humans and African apes
ME Johnson et al.
NATURE (2001)
Recent common ancestry of human Y chromosomes: Evidence from DNA sequence data
R Thomson et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2000)
Share Paper
