| BMC Bioinformatics | |
| SeqHound: biological sequence and structure database as a platform for bioinformatics research | |
| Katerina Michalickova1  Gary D Bader1  Michel Dumontier1  Hao Lieu1  Doron Betel1  Ruth Isserlin1  Christopher WV Hogue1  | |
| [1] Samuel Lunenfeld Research Institute, 600 University Avenue, Toronto, Ontario, Canada M5G 1X5 | |
| 关键词: local database resource; structure database; sequence database; | |
| Others : 1171919 DOI : 10.1186/1471-2105-3-32 |
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| received in 2002-08-01, accepted in 2002-10-25, 发布年份 2002 | |
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【 摘 要 】
Background
SeqHound has been developed as an integrated biological sequence, taxonomy, annotation and 3-D structure database system. It provides a high-performance server platform for bioinformatics research in a locally-hosted environment.
Results
SeqHound is based on the National Center for Biotechnology Information data model and programming tools. It offers daily updated contents of all Entrez sequence databases in addition to 3-D structural data and information about sequence redundancies, sequence neighbours, taxonomy, complete genomes, functional annotation including Gene Ontology terms and literature links to PubMed. SeqHound is accessible via a web server through a Perl, C or C++ remote API or an optimized local API. It provides functionality necessary to retrieve specialized subsets of sequences, structures and structural domains. Sequences may be retrieved in FASTA, GenBank, ASN.1 and XML formats. Structures are available in ASN.1, XML and PDB formats. Emphasis has been placed on complete genomes, taxonomy, domain and functional annotation as well as 3-D structural functionality in the API, while fielded text indexing functionality remains under development. SeqHound also offers a streamlined WWW interface for simple web-user queries.
Conclusions
The system has proven useful in several published bioinformatics projects such as the BIND database and offers a cost-effective infrastructure for research. SeqHound will continue to develop and be provided as a service of the Blueprint Initiative at the Samuel Lunenfeld Research Institute. The source code and examples are available under the terms of the GNU public license at the Sourceforge site http://sourceforge.net/projects/slritools/ webcite in the SLRI Toolkit.
【 授权许可】
2002 Michalickova et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| 20150420023230424.pdf | 342KB | ||
| Figure 4. | 41KB | Image | |
| Figure 3. | 89KB | Image | |
| Figure 2. | 67KB | Image | |
| Figure 1. | 37KB | Image |
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【 参考文献 】
- [1]Schuler GD, Epstein JA, Ohkawa H, Kans JA: Entrez: molecular biology database and retrieval system. Methods Enzymol 1996, 266:141-162.
- [2]Stoesser G, Baker W, van den BA, Camon E, Garcia-Pastor M, Kanz C, Kulikova T, Leinonen R, Lin Q, Lombard V, et al.: The EMBL Nucleotide Sequence Database. Nucleic Acids Res 2002, 30:21-26.
- [3]Bader GD, Hogue CW: BIND-a data specification for storing and describing biomolecular interactions, molecular complexes and pathways. Bioinformatics 2000, 16:465-477.
- [4]Bader GD, Donaldson I, Wolting C, Ouellette BF, Pawson T, Hogue CW: BIND-The biomolecular interaction network database. Nucleic Acids Res 2001, 29:242-245.
- [5]Betel D, Hogue CW: Kangaroo – A pattern-matching program for biological sequences. BMC Bioinformatics 2002, 3:20. BioMed Central Full Text
- [6]Michalickova K, Dharsee M, Hogue CWV: Sequence analysis on a 216 processor Beowulf cluster. 4th Annual Linux Showcase and Conference, Atlanta 2000, 4:111-119.
- [7]Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ: Basic local alignment search tool. J Mol Biol 1990, 215:403-410.
- [8]Dumontier M, Hogue CW: NBLAST: a cluster variant of BLAST for NxN comparisons. BMC Bioinformatics 2002, 3:13. BioMed Central Full Text
- [9]Benson DA, Karsch-Mizrachi I, Lipman DJ, Ostell J, Rapp BA, Wheeler DL: GenBank. Nucleic Acids Res 2002, 30:17-20.
- [10]Pruitt KD, Maglott DR: RefSeq and LocusLink: NCBI gene-centered resources. Nucleic Acids Res 2001, 29:137-140.
- [11]Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. Nucleic Acids Res 2000, 28:235-242.
- [12]Bairoch A, Apweiler R: The SWISS-PROT protein sequence database and its supplement TrEMBL in 2000. Nucleic Acids Res 2000, 28:45-48.
- [13]Boguski MS, Lowe TM, Tolstoshev CM: dbEST – database for "expressed sequence tags". Nat Genet 1993, 4:332-333.
- [14]Wang Y, Anderson JB, Chen J, Geer LY, He S, Hurwitz DI, Liebert CA, Madej T, Marchler GH, Marchler-Bauer A, et al.: MMDB: Entrez's 3D-structure database. Nucleic Acids Res 2002, 30:249-252.
- [15]Wu CH, Huang H, Arminski L, Castro-Alvear J, Chen Y, Hu ZZ, Ledley RS, Lewis KC, Mewes HW, Orcutt BC, et al.: The Protein Information Resource: an integrated public resource of functional annotation of proteins. Nucleic Acids Res 2002, 30:35-37.
- [16]Marchler-Bauer A, Panchenko AR, Shoemaker BA, Thiessen PA, Geer LY, Bryant SH: CDD: a database of conserved domain alignments with links to domain three-dimensional structure. Nucleic Acids Res 2002, 30:281-283.
- [17]The Gene Ontology Consortium: Creating the gene ontology resource: design and implementation. Genome Res 2001, 11:1425-1433.
- [18]Ostell JM, Kans JA: The NCBI data model. Methods Biochem Anal 1998, 39:121-144.
- [19]Bateman A, Birney E, Cerruti L, Durbin R, Etwiller L, Eddy SR, Griffiths-Jones S, Howe KL, Marshall M, Sonnhammer EL: The Pfam protein families database. Nucleic Acids Res 2002, 30:276-280.
- [20]Letunic I, Goodstadt L, Dickens NJ, Doerks T, Schultz J, Mott R, Ciccarelli F, Copley RR, Ponting CP, Bork P: Recent improvements to the SMART domain-based sequence annotation resource. Nucleic Acids Res 2002, 30:242-244.
- [21]Higgins DG, Sharp PM: CLUSTAL: a package for performing multiple sequence alignment on a microcomputer. Gene 1988, 73:237-244.
- [22]Thompson JD, Higgins DG, Gibson TJ: CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucleic Acids Res 1994, 22:4673-4680.
- [23]Chung SY, Wong L: Kleisli: a new tool for data integration in biology. Trends Biotechnol 1999, 17:351-355.
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