Related references
Note: Only part of the references are listed.Characterizing complex structural variation in germline and somatic genomes
Aaron R. Quinlan et al.
TRENDS IN GENETICS (2012)
High-Throughput Droplet Digital PCR System for Absolute Quantitation of DNA Copy Number
Benjamin J. Hindson et al.
ANALYTICAL CHEMISTRY (2011)
Mapping copy number variation by population-scale genome sequencing
Ryan E. Mills et al.
NATURE (2011)
Discovery and genotyping of genome structural polymorphism by sequencing on a population scale
Robert E. Handsaker et al.
NATURE GENETICS (2011)
Variation in Human Recombination Rates and Its Genetic Determinants
Adi Fledel-Alon et al.
PLOS ONE (2011)
E(nos)/CG4699 required fornanosfunction in the female germ line ofDrosophila
Lin Yu et al.
GENESIS (2010)
Origins and functional impact of copy number variation in the human genome
Donald F. Conrad et al.
NATURE (2010)
Transcriptome genetics using second generation sequencing in a Caucasian population
Stephen B. Montgomery et al.
NATURE (2010)
Integrating common and rare genetic variation in diverse human populations
David M. Altshuler et al.
NATURE (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)
Association of Trypanolytic ApoL1 Variants with Kidney Disease in African Americans
Giulio Genovese et al.
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)
Two Mammalian MOF Complexes Regulate Transcription Activation by Distinct Mechanisms
Xiangzhi Li et al.
MOLECULAR CELL (2009)
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Cristen J. Willer et al.
NATURE GENETICS (2009)
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Javier Simon-Sanchez et al.
NATURE GENETICS (2009)
Genetic Analysis of Variation in Human Meiotic Recombination
Reshmi Chowdhury et al.
PLOS GENETICS (2009)
Missing data imputation and haplotype phase inference for genome-wide association studies
Sharon R. Browning
HUMAN GENETICS (2008)
Evolutionary toggling of the MAPT 17q21.31 inversion region
Michael C. Zody et al.
NATURE GENETICS (2008)
Copy-number analysis goes more than skin deep
Steven A. McCarroll
NATURE GENETICS (2008)
Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease
Steven A. McCarroll et al.
NATURE GENETICS (2008)
Integrated detection and population-genetic analysis of SNPs and copy number variation
Steven A. McCarroll et al.
NATURE GENETICS (2008)
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)
A human protein complex homologous to the Drosophila MSL complex is responsible for the majority of histone H4 acetylation at lysine 16
ER Smith et al.
MOLECULAR AND CELLULAR BIOLOGY (2005)
A haplotype map of the human genome
D Altshuler et al.
NATURE (2005)
Segmental duplications and copy-number variation in the human genome
AJ Sharp et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
A common inversion under selection in Europeans
H Stefansson et al.
NATURE GENETICS (2005)
Linkage disequilibrium and association of MAPT H1 in Parkinson disease
L Skipper et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Share Paper
