Progress in the detection of human genome structural variations

Array comparative genomic hybridization (aCGH) analysis in Prader–Willi syndrome

(2008) Merlin G. Butler et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

De Novo Assembly and Genomic Structural Variation Analysis with Genome Sequencer FLX 3K Long-Tag Paired End Reads

(2008) Thomas Jarvie et al.   BIOTECHNIQUES

Emerging themes and new challenges in defining the role of structural variation in human disease

(2008) Andrew J. Sharp   HUMAN MUTATION

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

High-throughput sequencing provides insights into genome variation and evolution in Salmonella Typhi

(2008) Kathryn E Holt et al.   NATURE GENETICS

The functional impact of structural variation in humans

(2008) Matthew E. Hurles et al.   TRENDS IN GENETICS

Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array

(2007) Teresita Díaz de Ståhl et al.   HUMAN MUTATION