Completing the map of human genetic variation
- 9 May 2007
- journal article
- research article
- Published by Springer Nature in Nature
- Vol. 447 (7141), 161-165
- https://doi.org/10.1038/447161a
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- Global variation in copy number in the human genomeNature, 2006
- Genome assembly comparison identifies structural variants in the human genomeNature Genetics, 2006
- Linkage Disequilibrium and Heritability of Copy-Number Polymorphisms within Duplicated Regions of the Human GenomeAmerican Journal of Human Genetics, 2006
- Structural variation in the human genomeNature Reviews Genetics, 2006
- Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humansNature, 2006
- A high-resolution survey of deletion polymorphism in the human genomeNature Genetics, 2005
- A haplotype map of the human genomeNature, 2005
- Fine-scale structural variation of the human genomeNature Genetics, 2005
- A vision for the future of genomics researchNature, 2003
- Initial sequencing and analysis of the human genomeNature, 2001