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Methodological challenges of genome-wide association analysis in Africa

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The 1000 Genomes Project: new opportunities for research and social challenges

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Familial 14.5 Mb interstitial deletion 13q21.1-13q21.33: Clinical and array-CGH study of a benign phenotype in a three-generation family

(2009) Isabel Filges et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

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Genome-wide Copy-Number-Variation Study Identified a Susceptibility Gene, UGT2B17, for Osteoporosis

(2008) Tie-Lin Yang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history

(2008) P. M. Kim et al.   GENOME RESEARCH

Genotype, haplotype and copy-number variation in worldwide human populations

(2008) Mattias Jakobsson et al.   NATURE

Integrated detection and population-genetic analysis of SNPs and copy number variation

(2008) Steven A McCarroll et al.   NATURE GENETICS

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

(2008) Joshua M Korn et al.   NATURE GENETICS

wuHMM: a robust algorithm to detect DNA copy number variation using long oligonucleotide microarray data

(2008) Patrick Cahan et al.   NUCLEIC ACIDS RESEARCH