Bioinformatics. Группа авторов
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Internet Resources
Alliance of Genome Resources | www.alliancegenome.org |
Basic Local Alignment Search Tool (BLAST) | ncbi.nlm.nih.gov/BLAST |
ClinicalTrials.gov | clinicaltrials.gov |
DNA Data Bank of Japan (DDBJ) | www.ddbj.nig.ac.jp |
European Molecular Biology Laboratory–European Bioinformatics Institute (EMBL-EBI) | www.ebi.ac.uk |
GenBank | www.ncbi.nlm.nih.gov/genbank |
iCn3D | www.ncbi.nlm.nih.gov/Structure/icn3d/docs/icn3d_about.html |
Mouse Genome Database (MGD) | informatics.jax.org |
Online Mendelian Inheritance in Man (OMIM) | omim.org |
Protein Data Bank (PDB) | www.rcsb.org/pdb |
RefSeq | ncbi.nlm.nih.gov/refseq |
Single Nucleotide Polymorphism Database (dbSNP) | www.ncbi.nlm.nih.gov/SNP |
Vector Alignment Search Tool (VAST) | www.ncbi.nlm.nih.gov/Structure/VAST |
Zebrafish Information Network (ZFIN) | zfin.org |
Further Reading
1 Baxevanis, A.D. (2012). Searching Online Mendelian Inheritance in Man (OMIM) for information on genetic loci involved in human disease. Curr. Protoc. Hum. Genet. Chapter 9, Unit 9.13.1–10. A protocol-driven description of the basic methodology for formulating OMIM searches and a discussion of the types of information available through OMIM, including descriptions of clinical manifestations resulting from genetic abnormalities.
2 Galperin, M.Y., Fernández-Suárez, X.M., and Rigden, D.J. (2017). The 24th annual Nucleic Acids Research database issue: a look back and upcoming changes. Nucleic Acids Res. 45: D1–D11. A curated, annual review of specialized databases of interest and importance to the biomedical research community.
References
1 Altschul, S., Gish, W., Miller, W. et al. (1990). Basic local alignment search tool. J. Mol. Biol. 215: 403–410.
2 Amberger, J.S., Bocchini, C.A., Schiettecatte, F. et al. (2014). OMIM.org: Online Mendelian Inheritance in Man, an online catalog of human genes and genetic disorders. Nucleic Acids Res. 43: D789–D798.
3 Benson, D.A., Cavanaugh, M., Clark, K. et al. (2017). GenBank. Nucleic Acids Res. 45: D37–D42.
4 Bult, C.J., Eppig, J.T., Blake, J.A. et al. (2016). Mouse genome database 2016. Nucleic Acids Res. 44: D840–D847.
5 Collins, F.S., Patrinos, A., Jordan, E. et al., and Members of the DOE and NIH Planning Groups (1998). New goals for the U.S. Human Genome Project: 1998–2003. Science. 282: 682–689.
6 Collins, F.S., Green, E.D., Guttmacher, A.E., and Guyer, M.S., on behalf of the U.S. National Human Genome Research Institute (2003). A vision for the future of genomics research. Nature. 422: 835–847.
7 Finci, L.I., Krüger, N., Sun, X. et al. (2014). The crystal structure of netrin-1 in complex with DCC reveals the bifunctionality of netrin-1 as a guidance cue. Neuron. 83: 839–849.
8 Galperin, M.Y., Fernández-Suárez, X.M., and Rigden, D.J. (2017). The 24th annual Nucleic Acids Research database issue: a look back and upcoming changes. Nucleic Acids Res. 45: D1–D11.
9 Gao, J., Zhang, C., Yang, B. et al. (2012). Dcc regulates asymmetric outgrowth of forebrain neurons in zebrafish. PLoS One. 7: e36516.
10 Gibrat, J.-F., Madej, T., and Bryant, S. (1996). Surprising similarities in structure comparison. Curr. Opin. Struct. Biol. 6: 377–385.
11 Green, E.D. and Guyer, M.S., and The National Human Genome Research Institute (2011). Charting a course for genomic medicine from basepairs to bedside. Nature. 470: 204–213.
12 Howe, D.G., Bradford, Y.M., Conlin, T. et al. (2012). ZFIN, the Zebrafish Model Organism Database: increased support for mutants and transgenics. Nucleic Acids Res. 41: D854–D860.
13 International Human Genome Sequencing Consortium (2001). Initial sequencing and analysis of the human genome. Nature. 409: 860–921.
14 Madej, T., Lanczycki, C.J., Zhang, D. et al. (2014). MMDB and VAST+: tracking structural similarities between macromolecular complexes. Nucleic Acids Res. 42: D297–D303.
15 McKusick, V.A. (1966). Mendelian Inheritance in Man: Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes. Baltimore, MD: The Johns Hopkins University Press.
16 McKusick, V.A. (1998). Online Mendelian Inheritance in Man: Catalogs of Human Genes and Genetic Disorders, 12e. Baltimore, MD: The Johns Hopkins University Press.
17 Schmutz,