Human Genome Project

Brenner's Encyclopedia of Genetics: Second Edition

Volumn , Issue , 2013, Pages 552-554

  Bodmer, W ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

BAC; Base pair; Chromosome; CNV; Differential splicing; DNA; Enhancers; Genetic map; Genome; Genomics; Mutation; ORF; Positional cloning; Pseudogene; RNA

Indexed keywords

EID: 84940646593     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B978-0-12-374984-0.00746-4     Document Type: Chapter

References (11)

1. Clamp M., Fry B., Kamal M., et al. Distinguishing protein-coding and noncoding genes in the human genome. Proceedings of the National Academy of Sciences of the United States of America 2007, 104(49):19428-19433.
2. Finishing the euchromatic sequence of the human genome. Nature 2004, 431:931-945. International Human Genome Sequencing Consortium.
3. Kidd J.M., Cooper G.M., Donahue W.F., et al. Mapping and sequencing of structural variation from eight human genomes. Nature 2008, 453:56-64.
4. Pan Q., Shai O., Lee L.J., Frey B.J., Blencowe B.J. Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing. Nature Genetics 2008, 40(12):1413-1415.
5. Stankiewicz P., Lupski J.R. Structural variation in the human genome and its role in disease. Annual Review of Medicine 2010, 61:437-455.
6. Wang X.Q.D., Crutchley J.L., Dostie J. Shaping the genome with non-coding RNAs. Current Genomics 2011, 12:307-321.
7. GeneCards® http://www.genecards.org.
8. HUGO Gene Nomenclature Committee http://www.genenames.org.
9. Human Genome Project Information http://www.ornl.gov.
10. Oak Ridge National Laboratory http://www.ornl.gov.
11. Wellcome Trust Sanger Institute http://www.sanger.ac.uk.