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Nucleic Acids Research Advance Access originally published online on November 10, 2006
Nucleic Acids Research 2007 35(Database issue):D358-D362; doi:10.1093/nar/gkl825
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Nucleic Acids Research, 2007, Vol. 35, Database issue D358-D362
© 2006 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Articles

STRING 7—recent developments in the integration and prediction of protein interactions

Christian von Mering1,2,*, Lars J. Jensen1, Michael Kuhn1, Samuel Chaffron1,2, Tobias Doerks1, Beate Krüger1, Berend Snel3 and Peer Bork1,4

1 European Molecular Biology Laboratory, Meyerhofstrasse 1 69117 Heidelberg, Germany 2 University of Zurich, Winterthurerstrasse 190 8057 Zurich, Switzerland 3 Utrecht University, Padualaan 8 3584 CH Utrecht, The Netherlands 4 Max-Delbrück-Centre for Molecular Medicine, Robert-Rössle-Str. 10 13092 Berlin, Germany

*To whom correspondence should be addressed. Tel: +41 44 6353147; Fax: +41 44 6356864; Email: mering{at}molbio.unizh.ch

Received September 15, 2006. Revised October 5, 2006. Accepted October 5, 2006.


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 KNOWN AND PREDICTED INTERACTIONS
 NEW FEATURES AND IMPROVEMENTS...
 REFERENCES
 
Information on protein–protein interactions is still mostly limited to a small number of model organisms, and originates from a wide variety of experimental and computational techniques. The database and online resource STRING generalizes access to protein interaction data, by integrating known and predicted interactions from a variety of sources. The underlying infrastructure includes a consistent body of completely sequenced genomes and exhaustive orthology classifications, based on which interaction evidence is transferred between organisms. Although primarily developed for protein interaction analysis, the resource has also been successfully applied to comparative genomics, phylogenetics and network studies, which are all facilitated by programmatic access to the database backend and the availability of compact download files. As of release 7, STRING has almost doubled to 373 distinct organisms, and contains more than 1.5 million proteins for which associations have been pre-computed. Novel features include AJAX-based web-navigation, inclusion of additional resources such as BioGRID, and detailed protein domain annotation. STRING is available at http://string.embl.de/


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 KNOWN AND PREDICTED INTERACTIONS
 NEW FEATURES AND IMPROVEMENTS...
 REFERENCES
 
A fully comprehensive view of all functionally relevant protein interactions is still not available for any species, not even for relatively simple, single-celled model organisms. However, this information is essential for a systems-level understanding of cellular behavior, and it is needed in order to place the molecular functions of individual proteins into their cellular context.

For detecting direct physical binding between proteins, numerous small-scale and high-throughput experiments have been undertaken, and most of their reported interactions are available from dedicated interaction databases (14), as well as from multipurpose databases centered on specific model organisms (57). However, the growth of interaction data is severely lagging behind the pace of genome sequencing, so that for most genomes and proteins known to date no interaction data is available. Furthermore, proteins do not only interact physically: indirect associations such as genetic interactions or shared pathway memberships are equally important for a complete understanding of cellular function, but are for the most part not stored in interaction databases. Instead, they are available from a variety of pathway databases (8,9) and from the scientific literature.

The database STRING (‘Search Tool for the Retrieval of Interacting Genes/Proteins’) aims to collect, predict and unify most types of protein–protein associations, including direct and indirect associations. In order to cover organisms not yet addressed experimentally, STRING runs a set of prediction algorithms (10), and transfers known interactions from model organisms to other species based on predicted orthology of the respective proteins (11). STRING has grown from a purely predictive resource covering mainly prokaryotes (12) to a comprehensive tool integrating protein association information from all domains of life (Figure 1). Each interaction in the database is annotated with a benchmarked numerical confidence score, which can be used to filter the interaction network at any desired stringency. All data in STRING are stored in relational database tables. The interaction information is freely available for download, but download of the entire database content requires a license agreement to prevent redistribution (free for academic users who only access the previous version number).


Figure 1
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Figure 1 Protein interaction network in STRING. Screenshot from STRING showing a network of Saccharomyces cerevisiae proteins [the exosome complex, upper right, is seen weakly associated with proteins from nuclear transport, lower left, see also Ref. (26)]. The inset shows the context menu available for all STRING proteins—in the context menu, annotation and domain architecture are shown directly, and links to other databases and tools are available (22,23). In the network, links between proteins signify the various interaction data supporting the network, colored by evidence type (see STRING website for color legend).

 

    KNOWN AND PREDICTED INTERACTIONS
 TOP
 ABSTRACT
 INTRODUCTION
 KNOWN AND PREDICTED INTERACTIONS
 NEW FEATURES AND IMPROVEMENTS...
 REFERENCES
 
Known interactions in STRING are primarily imported from existing excellent interaction databases (15,8,9), and are complemented by automated text mining of PubMed abstracts and several other bodies of scientific text [such as from Ref. (6)]. As is the case for all interactions in STRING, imported interactions are mapped onto a consistent set of proteins and identifiers, thereby facilitating comparison between datasets. STRING does not store specific details regarding splicing isoforms or post-translational modifications, but instead reduces protein isoforms to a single protein per locus (usually as defined by the longest known protein-coding transcript). This level of resolution enables efficient storage and is compatible with most prediction/transfer algorithms, which usually operate only at the level of the gene locus.

Known interactions are further complemented by de novo interaction predictions derived from several comparative genomics prediction algorithms that are mainly applicable to prokaryotes (1319). These algorithms systematically compare genomes, searching for frequently observed gene neighborhoods, gene fusion events and similarities in gene occurrence across genomes. For each prediction algorithm, dedicated viewers of the genomic evidence are available in STRING.

Interaction evidence from model organisms is often useful for other organisms as well, especially when orthologs of interacting proteins can be clearly identified in the second organism. STRING systematically executes such orthology transfers, using both precomputed orthologs from the COG database (20), as well as a homology-based orthology scheme computed de novo (11). STRING can thus immediately predict a large number of interactions for any newly sequenced genome, as soon as it is included into the system. The combination of known, predicted and transferred interactions is unique, making STRING the most comprehensive interaction resource available to date, especially for organisms not addressed experimentally.

The homology data stored in STRING form the basis for the interaction transfers, and are the result of more than 7 x 1011 pairwise protein comparisons using the sensitive Smith–Waterman dynamic programming algorithm. This dataset is a very useful asset in itself [see also (21)], and can be accessed independently of the protein interaction networks by locally installing the STRING database files. Users of the website can also browse all of the homologs detected for any protein of interest, and can inspect alignments with very fast response times (Figure 2).


Figure 2
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Figure 2 Precomputed homology relations and alignments. For most genomes contained in STRING, sensitive all-against-all homology searches using the Smith–Waterman algorithm are included. These form the basis for assigning orthologs and transferring interaction information, but are also available directly to the user. Because they are stored in a relational database, access to homologs and alignments for any protein of interest is possible without the usual waiting time.

 

    NEW FEATURES AND IMPROVEMENTS IN STRING 7
 TOP
 ABSTRACT
 INTRODUCTION
 KNOWN AND PREDICTED INTERACTIONS
 NEW FEATURES AND IMPROVEMENTS...
 REFERENCES
 
The network viewer in STRING (Figure 1) is the central information source and navigation hub for the user. It has been extended through a context-sensitive menu-box, which displays associated information for any protein in the network. This menu includes a graphical summary of protein domains and features, and allows the user to link out to other external resources such as the motif discovery tool DILIMOT (22). STRING is now also tightly integrated with the SMART protein architecture research tool (23). With the latter it shares a common set of genomes and proteins, for which consistent results are pre-computed and stored. This enables automatic interlinking between both resources (SMART includes interaction previews, and STRING includes domain architecture previews). The topology and evolution of interaction networks can thus be studied both at the level of proteins as well as at the level of individual domains.

Since the last update (11), STRING has grown substantially both in terms of data sources and number of organisms covered. Five new databases are included [MINT, HPRD, BioGRID, DIP and Reactome (25,8)], as well as 194 new organisms. Especially due to this latter increase in completely sequenced organisms, the architecture of STRING had to be substantially upgraded so that it can accommodate present and future growth. With respect to the user interface, this required changes in the viewers for the genomic context data, which could no longer show all of the genomes simultaneously by default. Instead, STRING uses a phylogenetic tree of species to collapse redundant genomes; this tree has been derived from concatenated alignments of a small number of universal protein families (24). Users can navigate the tree by expanding or collapsing its sub-branches, thus choosing which organisms to focus on. AJAX technology (‘Asynchronous JavaScript and XML’) is then used to fetch the requested information into the existing, pre-loaded browser page, thus increasing useability and speed.

With respect to the underlying database structure, changes were necessary in the way homology data and interaction transfers are stored. Both can no longer be computed and stored in an ‘all-against-all’ fashion, because of their quadratic scaling with the number of genomes. Beginning with version 7, STRING therefore adopts a two-layered approach when accommodating fully sequenced genomes (Figure 3): important model organisms and those for which experimental data are available form the ‘core genomes’, all other genomes form the periphery. Within the core, homology searches and interaction transfers are still executed in an all-against-all fashion, whereas for peripheral genomes only searches against the core are included. These and other changes in STRING dramatically improve the scalability of the resource, leading to faster update cycles even when the number of sequenced genomes is to increase as fast as currently projected. Together with future plans to increase the scope and specificity of the stored interaction information, STRING should thus continue to facilitate not only network research but also wider projects that range from phylogenetics to metagenomics (24,25).


Figure 3
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Figure 3 Organisms covered by STRING. STRING currently contains 373 fully sequenced organisms. These are divided into ‘Core Organisms’ and ‘Peripheral Organisms’. The former include all important model organisms for which experimental data are available, as well as selected representatives for cases of redundant genome sequencing (e.g. when several closely related strains of a bacterial species have been sequenced, only one strain is included). The ‘Peripheral Organisms’ form the remainder; they tend to be somewhat redundant, and usually have little more than genomic sequence information annotated. For the core organisms, homology relations and interaction transfers are fully computed, whereas the peripheral organisms are only connected to the core but not among themselves (the graphic shows only a small selection of organisms; lines indicate homology searches and interaction transfers). This architecture allows STRING to encompass all sequenced genomes, while still keeping database size and computation time within reasonable limits.

 

    ACKNOWLEDGEMENTS
 
The authors wish to thank Dianna Fisk from the Saccharomyces Genome Database for access to the Gene Summary Paragraphs, and Toby Gibson, Martijn Huynen, Victor Neduva, Rune Linding and members of the Bork group for continued feedback and discussions. This work was supported in part by grants from the Bundesministerium für Forschung und Bildung, Germany, as well as through the ADIT Integrated Project, contract number LSHB-CT-2005-511065, and through the BioSapiens Network of Excellence, contract number LSHG-CT-2003-503265, both funded by the European Commission FP6 Programme. Funding to pay the Open Access publication charges for this article was provided by the University of Zurich, through its Research Priority Program ‘Systems Biology and Functional Genomics’.

Conflict of interest statement. None declared.


    Footnotes
 
The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors


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K. Stingl, K. Schauer, C. Ecobichon, A. Labigne, P. Lenormand, J.-C. Rousselle, A. Namane, and H. de Reuse
In Vivo Interactome of Helicobacter pylori Urease Revealed by Tandem Affinity Purification
Mol. Cell. Proteomics, December 1, 2008; 7(12): 2429 - 2441.
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Genome ResHome page
Y. Qi, Y. Suhail, Y.-y. Lin, J. D. Boeke, and J. S. Bader
Finding friends and enemies in an enemies-only network: A graph diffusion kernel for predicting novel genetic interactions and co-complex membership from yeast genetic interactions
Genome Res., December 1, 2008; 18(12): 1991 - 2004.
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BioinformaticsHome page
S. V. Rajagopala, J. Goll, N.D. D. Gowda, K. C. Sunil, B. Titz, A. Mukherjee, S. S. Mary, N. Raviswaran, C. S. Poojari, S. Ramachandra, et al.
MPI-LIT: a literature-curated dataset of microbial binary protein--protein interactions
Bioinformatics, November 15, 2008; 24(22): 2622 - 2627.
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Sci SignalHome page
M. B. Major, B. S. Roberts, J. D. Berndt, S. Marine, J. Anastas, N. Chung, M. Ferrer, X. Yi, C. L. Stoick-Cooper, P. D. von Haller, et al.
New Regulators of Wnt/{beta}-Catenin Signaling Revealed by Integrative Molecular Screening
Sci. Signal., November 11, 2008; 1(45): ra12 - ra12.
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Nucleic Acids ResHome page
M. A. A. Castro, R. J. S. Dalmolin, J. C. F. Moreira, J. C. M. Mombach, and R. M. C. de Almeida
Evolutionary origins of human apoptosis and genome-stability gene networks
Nucleic Acids Res., November 1, 2008; 36(19): 6269 - 6283.
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Physiol. GenomicsHome page
E. W. Deutsch, H. Lam, and R. Aebersold
Data analysis and bioinformatics tools for tandem mass spectrometry in proteomics
Physiol Genomics, October 8, 2008; 33(1): 18 - 25.
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Proc. Natl. Acad. Sci. USAHome page
N. Ruiz
Bioinformatics identification of MurJ (MviN) as the peptidoglycan lipid II flippase in Escherichia coli
PNAS, October 7, 2008; 105(40): 15553 - 15557.
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Physiol. GenomicsHome page
N. Tiffin, I. Okpechi, C. Perez-Iratxeta, M. A. Andrade-Navarro, and R. Ramesar
Prioritization of candidate disease genes for metabolic syndrome by computational analysis of its defining phenotypes
Physiol Genomics, September 17, 2008; 35(1): 55 - 64.
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J. Virol.Home page
M. E. McLaughlin-Drubin, K.-W. Huh, and K. Munger
Human Papillomavirus Type 16 E7 Oncoprotein Associates with E2F6
J. Virol., September 1, 2008; 82(17): 8695 - 8705.
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BioinformaticsHome page
S. F. Saccone, N. L. Saccone, G. E. Swan, P. A. F. Madden, A. M. Goate, J. P. Rice, and L. J. Bierut
Systematic biological prioritization after a genome-wide association study: an application to nicotine dependence
Bioinformatics, August 15, 2008; 24(16): 1805 - 1811.
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MicrobiologyHome page
F. Santos-Beneit, A. Rodriguez-Garcia, E. Franco-Dominguez, and J. F. Martin
Phosphate-dependent regulation of the low- and high-affinity transport systems in the model actinomycete Streptomyces coelicolor
Microbiology, August 1, 2008; 154(8): 2356 - 2370.
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BioinformaticsHome page
J. Goll, S. V. Rajagopala, S. C. Shiau, H. Wu, B. T. Lamb, and P. Uetz
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Bioinformatics, August 1, 2008; 24(15): 1743 - 1744.
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Mol Biol EvolHome page
B. E. Dutilh, B. Snel, T. J. G. Ettema, and M. A. Huynen
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Mol. Biol. Evol., August 1, 2008; 25(8): 1659 - 1667.
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Brief BioinformHome page
Z. Hu, E. S. Snitkin, and C. DeLisi
VisANT: an integrative framework for networks in systems biology
Brief Bioinform, July 1, 2008; 9(4): 317 - 325.
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Mol. Cell. Biol.Home page
M.-E. Caruso, S. Jenna, M. Bouchecareilh, D. L. Baillie, D. Boismenu, D. Halawani, M. Latterich, and E. Chevet
GTPase-Mediated Regulation of the Unfolded Protein Response in Caenorhabditis elegans Is Dependent on the AAA+ ATPase CDC-48
Mol. Cell. Biol., July 1, 2008; 28(13): 4261 - 4274.
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BioinformaticsHome page
M. T. Dittrich, G. W. Klau, A. Rosenwald, T. Dandekar, and T. Muller
Identifying functional modules in protein-protein interaction networks: an integrated exact approach
Bioinformatics, July 1, 2008; 24(13): i223 - i231.
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Nucleic Acids ResHome page
J. Klein, S. Leupold, R. Munch, C. Pommerenke, T. Johl, U. Karst, L. Jansch, D. Jahn, and I. Retter
ProdoNet: identification and visualization of prokaryotic gene regulatory and metabolic networks
Nucleic Acids Res., July 1, 2008; 36(suppl_2): W460 - W464.
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Nucleic Acids ResHome page
B. E. Dutilh, Y. He, M. L. Hekkelman, and M. A. Huynen
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Nucleic Acids Res., July 1, 2008; 36(suppl_2): W470 - W474.
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Nucleic Acids ResHome page
C.-Y. Lin, C.-H. Chin, H.-H. Wu, S.-H. Chen, C.-W. Ho, and M.-T. Ko
Hubba: hub objects analyzer--a framework of interactome hubs identification for network biology
Nucleic Acids Res., July 1, 2008; 36(suppl_2): W438 - W443.
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Nucleic Acids ResHome page
L.-C. Tranchevent, R. Barriot, S. Yu, S. Van Vooren, P. Van Loo, B. Coessens, B. De Moor, S. Aerts, and Y. Moreau
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Nucleic Acids Res., July 1, 2008; 36(suppl_2): W377 - W384.
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Nucleic Acids ResHome page
C. E. Martinez-Guerrero, R. Ciria, C. Abreu-Goodger, G. Moreno-Hagelsieb, and E. Merino
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S. Brohee, K. Faust, G. Lima-Mendez, O. Sand, R. Janky, G. Vanderstocken, Y. Deville, and J. van Helden
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Int. J. Syst. Evol. Microbiol.Home page
D. C. Teixeira, S. Eveillard, P. Sirand-Pugnet, A. Wulff, C. Saillard, A. J. Ayres, and J. M. Bove
The tufB-secE-nusG-rplKAJL-rpoB gene cluster of the liberibacters: sequence comparisons, phylogeny and speciation
Int J Syst Evol Microbiol, June 1, 2008; 58(6): 1414 - 1421.
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Mol. Cell. ProteomicsHome page
D. Li, W. Liu, Z. Liu, J. Wang, Q. Liu, Y. Zhu, and F. He
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Mol. Cell. Proteomics, June 1, 2008; 7(6): 1043 - 1052.
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Z. Mashhadi, H. Zhang, H. Xu, and R. H. White
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J. Bacteriol., April 1, 2008; 190(7): 2615 - 2618.
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BioinformaticsHome page
I. V. Tetko, I. V. Rodchenkov, M. C. Walter, T. Rattei, and H.-W. Mewes
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Bioinformatics, March 1, 2008; 24(5): 621 - 628.
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J R Soc InterfaceHome page
P. R Kensche, V. van Noort, B. E Dutilh, and M. A Huynen
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J R Soc Interface, February 6, 2008; 5(19): 151 - 170.
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B. W. Davies and G. C. Walker
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BioinformaticsHome page
G. Moreno-Hagelsieb and K. Latimer
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Bioinformatics, February 1, 2008; 24(3): 319 - 324.
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L. J. Jensen, P. Julien, M. Kuhn, C. von Mering, J. Muller, T. Doerks, and P. Bork
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Nucleic Acids Res., January 11, 2008; 36(suppl_1): D250 - D254.
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C. Su, J. M. Peregrin-Alvarez, G. Butland, S. Phanse, V. Fong, A. Emili, and J. Parkinson
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F. Diella, C. M. Gould, C. Chica, A. Via, and T. J. Gibson
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R. Linding, L. J. Jensen, A. Pasculescu, M. Olhovsky, K. Colwill, P. Bork, M. B. Yaffe, and T. Pawson
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Nucleic Acids ResHome page
P. Pagel, M. Oesterheld, O. Tovstukhina, N. Strack, V. Stumpflen, and D. Frishman
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Nucleic Acids ResHome page
M. Kuhn, C. von Mering, M. Campillos, L. J. Jensen, and P. Bork
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Nucleic Acids Res., January 11, 2008; 36(suppl_1): D684 - D688.
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BioinformaticsHome page
A.D.J. van Dijk, C.J.F. ter Braak, R.G. Immink, G.C. Angenent, and R.C.H.J. van Ham
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BioinformaticsHome page
R. Varshavsky, A. Gottlieb, D. Horn, and M. Linial
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Bioinformatics, December 15, 2007; 23(24): 3343 - 3349.
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J. Livny, Y. Yamaichi, and M. K. Waldor
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J. Bacteriol., December 1, 2007; 189(23): 8693 - 8703.
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B. S. Srinivasan, N. H. Shah, J. A. Flannick, E. Abeliuk, A. F. Novak, and S. Batzoglou
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C. M. Arraiano, J. Bamford, H. Brussow, A. J. Carpousis, V. Pelicic, K. Pfluger, P. Polard, and J. Vogel
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R. W. Shultz, V. M. Tatineni, L. Hanley-Bowdoin, and W. F. Thompson
Genome-Wide Analysis of the Core DNA Replication Machinery in the Higher Plants Arabidopsis and Rice
Plant Physiology, August 1, 2007; 144(4): 1697 - 1714.
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Nucleic Acids ResHome page
C. Perez-Iratxeta, P. Bork, and M. A. Andrade-Navarro
Update of the G2D tool for prioritization of gene candidates to inherited diseases
Nucleic Acids Res., July 13, 2007; 35(suppl_2): W212 - W216.
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Nucleic Acids ResHome page
P. Smits, J. A. M. Smeitink, L. P. van den Heuvel, M. A. Huynen, and T. J. G. Ettema
Reconstructing the evolution of the mitochondrial ribosomal proteome
Nucleic Acids Res., July 9, 2007; 35(14): 4686 - 4703.
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BioinformaticsHome page
G. Dawelbait, C. Winter, Y. Zhang, C. Pilarsky, R. Grutzmann, J.-C. Heinrich, and M. Schroeder
Structural templates predict novel protein interactions and targets from pancreas tumour gene expression data
Bioinformatics, July 1, 2007; 23(13): i115 - i124.
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