Linkage studies often yield intervals containing several hundred positional candidate genes. Different manual or automatic approaches exist for the determination of the gene most likely to cause the disease. While the manual search is very flexible and takes advantage of the researchers' background knowledge and intuition, it may be very cumbersome to collect and study the relevant data. Automatic solutions on the other hand usually focus on certain models, remain “black boxes” and do not offer the same degree of flexibility.
We have developed a web-based application that combines the advantages of both approaches. Information from various data sources such as gene-phenotype associations, gene expression patterns and protein-protein interactions was integrated into a central database. Researchers can select which information for the genes within a candidate interval or for single genes shall be displayed. Genes can also interactively be filtered, sorted and prioritised according to criteria derived from the background knowledge and preconception of the disease under scrutiny.
GeneDistiller provides knowledge-driven, fully interactive and intuitive access to multiple data sources. It displays maximum relevant information, while saving the user from drowning in the flood of data. A typical query takes less than two seconds, thus allowing an interactive and explorative approach to the hunt for the candidate gene.
GeneDistiller can be freely accessed at http://www.genedistiller.org
Citation: Seelow D, Schwarz JM, Schuelke M (2008) GeneDistiller—Distilling Candidate Genes from Linkage Intervals. PLoS ONE 3(12): e3874. https://doi.org/10.1371/journal.pone.0003874
Editor: Philip Awadalla, University of Montreal, Canada
Received: July 24, 2008; Accepted: November 10, 2008; Published: December 5, 2008
Copyright: © 2008 Seelow et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The work has been supported by funds of the NeuroCure Clinical Research Centre of the Charité Berlin, and by the Deutsche Forschungsgemeinschaft (SFB665 TP A6 to M.S.)
Competing interests: The authors have declared that no competing interests exist.
In recent years, genetic defects have been discovered for many monogenic diseases through linkage analysis, candidate gene approaches or a combination thereof. Crucial for this success were the access to large affected families in sufficient numbers or the availability of animal models that closely mimicked the human disease phenotype. However, of more than 25,000 human protein coding genes listed in the Entrez database, less than 2,000 have been associated with human disease phenotypes . Geneticists are increasingly confronted with smaller families affected with rare conditions that carry “private” mutations. Nevertheless, elucidation of the gene defects in such single families has opened whole new research areas (e.g. the KE family for FOXP2  in language development and the “Muscle baby” for Myostatin in muscle research , ). Linkage analyses of these small pedigrees have thus to be performed with relatively few meioses leading to more than one or to larger candidate intervals over 10 cM, whose LOD scores may remain below the threshold for significance of 3. Such large intervals may contain several hundred genes that have to be prioritised for mutation screening before labour and cost intensive gene sequencing is initiated.
The conventional manual approach usually does not follow any strict algorithm but is guided by the background knowledge and expectations of the researcher (Figure 1). In a conventional setting, this involves a search for all known genes in the linkage interval and a subsequent query of different databases to gather available data and extract the relevant information for prioritisation. Assessment of the validity of a positional candidate requires a thorough knowledge of many data relevant to the gene or protein of interest. Most of this information can be found on the Internet, but it is tedious to collect the fragments from different data sources. While some tools offer maps showing all genes within a region (NCBI MapViewer , UCSC Genome Browser ) without any gene-specific information, others (GeneCards ) feature detailed genetic data but only for one single gene at a time. Besides, all these tools suffer from the lack of more elaborate query options refining the output to a well-defined group of genes.
This scheme illustrates different approaches to choose reasonable candidate genes from a linkage interval. The researcher can either follow a hypothesis driven approach based on a functional model or simply choose genes based on single properties reflecting the likelihood of being disease causing, e.g. the co-expression with other disease genes that cause similar phenotypes. The general concepts are depicted as pink boxes, gene properties that can be queried by GeneDistiller as yellow boxes, and properties or models GeneDistiller presently does not offer as blue boxes. With GeneDistiller, the user is absolutely free to combine gene properties according to her or his own hypotheses.
In the past, several interactive, automatic or semiautomatic approaches to search for disease genes have been proposed  or implemented such as Endeavour , GeneWanderer , GeneSeeker , GeneSniffer (http://www.genesniffer.org/), PosMed (http://omicspace.riken.jp/PosMed/) and SUSPECTS . Some applications classify genes based on sequence features , or use protein-protein interaction networks ,  while others (GeneSeeker, SUSPECTS) combine different approaches. For the researchers, however, the algorithms of these programs remain largely inaccessible. In a meta-test of three software tools for automatic gene prioritisation of positional candidate genes the authors recommend to exert caution in relying solely on single positional candidate prioritisation tools . In any case, a researcher would usually want to read relevant gene specific information for the proposed candidate genes her- or himself before embarking upon a large sequencing project.
GeneDistiller is aimed at various strategies. It can either be used as a tool to query, select and project genes from within a linkage interval together with gene specific data or to display rich information on human candidate genes obtained with other prioritisation tools or of the researcher's interest. Besides, it offers a customisable user-driven prioritisation integrating the available data as specified by the researcher. The application is web-based and features an intuitive interface which enables the researcher to formulate simple queries without the need to read a software manual before, yet allowing more complex queries. The software returns all results on one HTML page which can easily be printed or saved. The kind of information included is determined by the researcher. Since the results of a search are presented on the fly, the software offers a high degree of interactivity, allowing the researcher to quickly change some parameters to follow new ideas which may arise when reading the results. She can thus explore the data with the help of the computer and combine newly gained insights with her background knowledge (Figure 2).
The user-friendly interface allows the researchers to incorporate their background knowledge about diseases and genes into the interactive “gene distilling” process. They can extract all the information relevant to their specific question at our one-stop shop. This saves them from drowning in the flood of data available on the WWW and helps them to determine the most promising candidates.
GeneDistiller offers different approaches to determine the most likely candidate genes:
GeneDistiller can list all genes within a linkage interval together with gene specific information. Among the different kinds of gene specific data, the researcher can select those relevant to her and print and read this information for all positional candidates to choose the most promising gene. This approach can be very helpful if she has only a vague idea of the disease causing gene.
The researcher can apply filters to the genes in the linkage interval, thus narrowing down their number to a small group of more promising candidates (Figure 3). This approach should be applied when the researcher is able to define conditions that must be fulfilled by the candidate gene, e.g. expression in a certain tissue or co-expression with another gene. Alternatively, “visual” filters can be used to highlight gene properties so that no gene will be excluded.
This figure shows how filters can be applied in GeneDistiller to reduce the number of genes to be studied. After defining the linkage interval, more and more selection criteria can be added by the researcher, narrowing down the genes to ever more likely candidates. The example depicts the hunt for candidate genes for epilepsy in a 60 Mbp region on chromosome 2. The size of a rectangle is proportional to the number of genes and the grey shades reflect the “distillation” process in which the best candidates are enriched.
Genes can be sorted according to certain parameters, e.g. their position, tissue specific expression or likelihood to encode mitochondrial proteins.
GeneDistiller offers a user-driven prioritisation function which ranks genes according to the researcher's specifications. Prioritisation approaches should be used when the researcher cannot exclude any gene in advance but wants to focus on the genes in falling order of “apparent” relevance.
The user is free to combine these methods to follow a strategy which best suits the problem, e.g. she can exclude genes using filters, choose the parameters to be used in the prioritisation process, select those to be displayed in the output and highlight interesting properties.
Application of the different strategies
While some researchers prefer to read the available information for all genes within a candidate interval, others may rather narrow down the number of genes beforehand and focus on those fulfilling certain conditions that are regarded as mandatory. We describe the application of the two latter approaches which are more complex and most commonly used, selection (filtering) and prioritisation, here together with valid “real life” examples. More examples are given on our website and help page.
Selection (Figure 3).
Imagine, a candidate locus for epilepsy could be mapped to a 60 Mbp region on chromosome 2. Entering the markers limiting the interval will yield 362 genes. Since epilepsy is a common disease and a well-studied subject, the researcher might wish to focus on those genes that are known to show a suitable phenotype in an animal model. She thus filters the genes for their described mouse phenotypes. By selecting nervous system phenotype and behaviour/neurological phenotype from the MGD phenotypes drop-down menu and limiting the query to the respective genes, the number of genes can be significantly reduced to 35 genes which are linked to at least one of these phenotypes. A further condensation can be reached when the descriptions for human phenotypes are considered: The researcher enters the broad term brain into the field highlight these keywords and restricts the search to genes in whose descriptions one of these keywords appear. The more specific word epilepsy is not used because she does not want to restrain her search to genes already known to cause epilepsy in humans. The list now contains 25 candidate genes. Since a gene responsible for epilepsy is likely to be expressed in brain, she now opens the expression tab and selects >1 (x median) for the expression in whole brain. Restriction to the genes with an expression above the median can be reached when show only genes fulfilling the conditions is selected and will yield 17 genes. From functional studies with her patients she knows that the prefrontal cortex might be involved and decides to focus on genes with a notable expression there. Setting a filter for prefrontal cortex expression >3 (x median) and connecting both expression filters with AND shortens the list to only 7 genes. As many epilepsy genes involve ion channels she could further reduce the number of genes by adding the Gene Ontology ID for ion transport (GO:0006811) into the highlight these GO IDs fields and restrict the search to those carrying this GO ID or a subclass. Now, only 2 genes, SCN1A and SCN3A remain in the list both of which are excellent candidates for an epilepsy phenotype.
For prioritisation the researcher can easily incorporate his or her background knowledge and follow various search avenues alone or in combination. GeneDistiller features predefined models suitable for the common approaches for prioritisation. In the output, GeneDistiller shows scores for each of the parameters chosen for the prioritisation so that the researcher can easily modify the weights given to the different parameters if she wants to shift the focus to certain aspects.
The disease under investigation may have a similar phenotype as a disease with a known gene defect or a transgenic mouse model. In this case the search comprises genes within the candidate region that are either known to be causing a similar phenotype in humans or mice or relate to disease-causing genes by experimentally proven protein-protein interactions, function in the same biochemical or signal transduction pathway, sequence similarities, similar protein domains or entries in the Gene Ontology  or share similar mRNA expression patterns. The latter approach stands in analogy to the credo of the neurophysiologist “Neurons that fire together, wire together”, changed into “Disease-linked genes more or less, co-express”. The set of known disease genes can either be defined by their gene symbol or gene ID or retrieved from the database by specifying suitable OMIM IDs or terms.
Genes may also be prioritised according to their suspected functional properties. The positional candidate may belong to a certain functional group of genes (e.g. various sodium channel proteins in Generalised Epilepsy with Febrile Seizures (GEFS+) ), biochemical pathways (e.g. O-glycolysation defects in congenital myopathies; FCMD, POMGNT1, POMT1, POMT2, LARGE ) or sub-cellular organelles (e.g. impaired mitochondrial protein synthesis in mutations of mitochondrial elongation factors EFG1 and TSFZ , ).
Let us imagine the same situation as depicted in the example for the selection approach with the same linkage interval. Instead of filtering the data for genes fulfilling all criteria, the genes within the linkage interval can also be prioritised according to their similarity to genes already known to cause epilepsy. Here, the predefined model prioritise with focus on possible pathways is chosen. We apply all our background knowledge to the query, i.e. we want to focus on genes with the assigned term brain, with known nervous system phenotype or behaviour/neurological phenotype in mice, expression in the relevant tissues and phenotypic, functional and expression similarities with genes known to be involved in epilepsy (Figure 4). As with the filtering approach, the best candidate, SCN1A, appears on top of the list. Here, however, no genes are discarded so that the researcher can scroll from the most to the least promising candidate, read the gene specific data and also their accordance to the prioritisation model as a whole and for every single parameter (Figure 5).
This figure shows the query interface of GeneDistiller for the prioritisation example for epilepsy described in the text. The interface is divided into different sections in which the parameters describing a similar aspect of the gene-specific data are listed. Sections not used can be closed (e.g. “prioritisation settings”). Please note that most of the available tissues in the expression section are omitted to improve readability.
GeneDistiller prints all results on a single HTML page. The genes are listed in the selected order, in case of prioritisation strategies also with their over-all scores and sub scores for different parameters. The gene specific data is presented with hyperlinks to the original data sources. Keywords or values that were used for filtering or highlighting are printed in bold letters. The same applies to values that are present in other genes known to be related with the selected disease (epilepsy, in this case). Please note that many NCBI GeneRIFs and OMIM reports for SCN1A were omitted in this figure to improve readability.
Database schema and contents
The GeneDistiller database stores data from various sources that are most frequently considered by researchers when manually searching for candidate genes. All gene-specific data is stored in satellite tables connected to a central database table GENES in which the genes are defined. These connections are either modelled as 1∶1, 1∶n or m∶n relations, depending on the nature of the data. The database schema therefore resembles the query-optimised star schema found in many data warehouses (the database schema can be found on GeneDistiller's website). Whenever database entities are defined by a stable numeric ID in their original environment, GeneDistiller uses this ID to facilitate later updates and hyperlinks to the original source. If such an ID is not available and m∶n relations must be modelled, an internal serial numeric ID is used instead. This is also the case when data from different sources are mixed in one table, e.g. for SNP markers which are not all necessarily included in dbSNP. In the schema, SNP and STR markers are not directly connected to the genes. If marker and gene information is mixed in a query, their physical position will be used.
The database schema makes extensive use of constraints to guarantee referential integrity and to exclude worthless information (e.g. genetic markers without a position). Dubious data (e.g. markers with more than one position, except for gonosomal markers) is either excluded or this state is indicated.
GeneDistiller includes the following data: Genes, gene positions, gene RIFs, gene ontology, cellular localisation of gene products, transcripts, exons, OMIM reports, mouse phenotypes, protein-protein interactions, gene expression data, protein domains, SNP markers, STR markers. A list of the external data presently integrated in GeneDistiller is given in Table 1. More data will be added in the future according to our and the community's needs. Whenever such data is displayed, a hyperlink to the original data source is generated so that users have the chance to easily drill-down the information. Besides, links to Genbank files via BioMart  and to Exon-Primer (http://ihg2.helmholtz-muenchen.de/ihg/ExonPrimer.html) are presented so that the researchers can directly choose their sequencing primers without the need to manually query a sequence database.
The data stored in the database is updated in regular intervals of 3 months. Further updates are performed whenever new data sources are integrated. Here again, the strict quality control measures described above are applied. Whenever data is queried, a time-stamp is printed indicating the last update or version of the data.
GeneDistiller is web-based; all interfaces are ordinary HTML pages without any Java applications to be installed. In the query interface (Figure 4), parameters are grouped into distinct blocks. Some more advanced parameters such as tissue-specific expression are not shown by default but all blocks can be switched on and off at the researcher's will.
To use GeneDistiller, in a first step, the possible candidate genes have to be chosen. They can either be positional candidates from a linkage interval or functional candidates. In the former case, the interval can be defined by entering its position or limiting markers, in the latter case, gene symbols or Entrez gene IDs can be specified. The researcher can now select which information shall be included in the output (or stick to the default settings suitable for a first glance). Using these settings, the selected data would be shown for all genes within the candidate interval.
To reduce the number of genes, filters can be applied by specifying conditions. These can be defined either by selecting one or more values from select boxes (when only a limited number of values is stored in the respective database table, e.g. mouse phenotypes) or by typing values. Depending on the parameter, the corresponding property table is either searched for tuples with exactly this value (e.g. GO IDs) or a full-text search is performed (e.g. OMIM reports). When numeric values are stored in the database, comparison operators (<, = , >) can be applied (e.g. for gene expression data). When the researcher does not want to exclude genes but to emphasise those fulfilling the conditions, the highlighting function can be used. In this case, keywords occurring in the text or matching values will be printed in bold and, in full-text, colour.
GeneDistiller supports the researcher with the option to sort or prioritise the genes so that the more likely candidates appear on top of the list. For sorting, a single parameter such as expression similarity or likelihood of incorporation into mitochondria can be chosen. Prioritisation offers even broader possibilities as different parameters can be combined into the ranking. The researcher can choose between different predefined settings for different prioritisation strategies (which focus on distinct approaches, e.g. similarity or tissue-specificity) and is absolutely free to choose further parameters to be included or lay more or less weight on any of them. When prioritisation is applied, a detailed prioritisation score is printed for each gene so that it becomes clear which parameter causes a gene to be highly ranked. Since a typical query takes less than 2 seconds, the researcher can easily modify his or her prioritisation settings on the basis of the results. The whole prioritisation process is therefore completely transparent and user-driven and allows a fast, intuitive, interactive and explorative access to the results.
GeneDistiller prints the results of a query in HTML format. The resulting page (Figure 5) does not make use of colour unless to highlight keywords chosen by the user. The genes are presented together with all the desired data in an order specified by the researcher and visually separated to increase readability. The page also includes hyperlinks to the original data to simplify access to more detailed data which might exist on the website of the data source. Below the actual data, a timestamp or version of the data is displayed. The page can be printed or saved for later use. The output also features two hyperlinks, one to the results page and one to the query interface with all current settings. Bookmarking this hyperlink allows a researcher to return to the query interface and change the query at any time without having to fill out the form once again. It can also be shared with other researchers so that they can refine the search on the basis of their own background knowledge or focus and eventually return their concept as another bookmarked query instead of a static list of genes.
GeneDistiller can also be called and used from other applications. Since all settings, e.g. regions, gene lists, information to be displayed filtering criteria etc., can be specified in the call, GeneDistiller can easily be integrated into other applications. This can be especially worthwhile for prioritisation tools which could extend their list of suggested candidate genes with gene specific data from GeneDistiller, hence facilitate the decision to exclude certain genes from sequencing.
GeneDistiller is aimed at the geneticists themselves. We have therefore developed an interface that is relatively easy to use. While this makes the use of GeneDistiller quite intuitive, queries with a high degree of complexity are not feasible. For example, filters for different kinds of data are always joined by AND. While an interface allowing to enter the Boolean logic might be useful to some bioinformaticians, we believe that it would tend to confuse the majority of geneticists.
Our software differs from the existing prioritisation tools because we deeply integrate the geneticist into the gene hunting process. In our opinion, the researcher's background knowledge and the human mind's capabilities to spontaneously associate information bear a potential that is neglected by automatic solutions. In these, the researcher can give some information about the nature of the disease before the data mining begins and exclude (negatively select) suggested candidates afterwards but he is not able to quickly apply his background knowledge in between, i.e. on the basis of the results. This is further complicated because most prioritisation tools lack the capability to display gene specific data comprehensively. Reading the rich information printed by GeneDistiller could also lead the researcher spontaneously to completely new ideas, he might thus discover something he did not expect.
However, GeneDistiller is not meant as a replacement for the existing prioritisation tools. It does for example not at all offer the same degree of sequence comparisons or evaluation of interaction networks, calculations in which computers easily outperform humans. We regard our software and automatic solutions as supplemental approaches which should be combined when a prioritisation strategy is applied. If a researcher decides to solely rely on automatic prioritisation, GeneDistiller could be a valuable resource to gather information about the candidate genes to exclude some of them before the cost-intensive sequencing process is started.
At present, GeneDistiller only offers information about human genes. We are currently integrating mouse data, as mice are often used as a model organism in gene hunting. Depending on the use of GeneDistiller by the community and suggestions from the users, other species, especially rat, might be added in the future.
The GeneDistiller database runs on PostgreSQL 8 under Debian Linux on an Intel QuadCore server with 8 GB of RAM. It uses a strictly conventional schema, no special data types or objects are used. Tables are connected with foreign keys to ensure referential integrity. The database schema is query-optimised and makes use of indexes whenever an attribute is referenced or frequently included in queries.
The software behind the interfaces was programmed in Perl 5.8. Submitted data is read using the CGI module, HTML::Template is used to create the query interface, database connections are made with the DBI module and the DBD::Pg database driver, bar charts are created with the GD module and the Statistics::Basic::Correlation module is used to calculate Pearson correlation for expression data.
Expression similarity is calculated using Pearson correlation. For this, the mean expression in any available tissue is used. This value can be used for prioritisation (multiplied by the user-defined weight), sorting and filtering. In the latter case, only genes with a correlation higher than the specified factor are shown.
The computation of the similarity of the user specified tissue specific expression is performed by comparison of each tissue's expression/median with the specified value. If the value is above the user input and the operator is ‘greater then’ or if it is below and ‘smaller then’ was selected, a positive score will be generated; in other cases the score will be negative. The score is calculated by division of the real expression/median by the user entered value, if the result is negative, the inverse will be taken. All scores for one gene are added to generate the final similarity score.
Querying fields with a hierarchical structure (e.g. GeneOntology) will also find descendants (subclasses) of an entity, e.g. querying for DNA repair will also find genes, which do not carry this term but its subclasses base-excision repair or mismatch repair instead. To achieve this, a recursive query is carried out using a PL/pgSQL function. Results are written into a temporary table and then used by GeneDistiller to either restrict a query or to highlight values (or their subclasses) matching the user's request.
The query interface and the results page accept input submitted as GET or POST requests and will generate and return the according HTML page. All settings which can be made in the query interface can also be included in such a call. A complete list of the options with examples is given on GeneDistiller's website. Please note that the use of the data collected in GeneDistiller might require a license.
The authors thank Kristina Jülich for reviewing the manuscript and the many colleagues who beta-tested the application, encouraged us and suggested improvements.
Conceived and designed the experiments: DS MS. Performed the experiments: DS JMS. Analyzed the data: DS JMS MS. Contributed reagents/materials/analysis tools: DS JMS. Wrote the paper: DS JMS MS. Had the idea and the conception to the software: MS. Has written most of the code and part of the article: DS. Wrote some of the code, did extensive beta-testing of the software, conceived the examples: JMS.
- 1. Hamosh A, Scott AF, Amberger JS, Bocchini CA, McKusick VA (2005) Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders. Nucleic Acids Res 33: D514–D517.A. HamoshAF ScottJS AmbergerCA BocchiniVA McKusick2005Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.Nucleic Acids Res33D514D517
- 2. Lai CS, Fisher SE, Hurst JA, Vargha-Khadem F, Monaco AP (2001) A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 413: 519–523.CS LaiSE FisherJA HurstF. Vargha-KhademAP Monaco2001A forkhead-domain gene is mutated in a severe speech and language disorder.Nature413519523
- 3. Schuelke M, Wagner KR, Stolz LE, Hubner C, Riebel T, et al. (2004) Myostatin mutation associated with gross muscle hypertrophy in a child. N Engl J Med 350: 2682–2688.M. SchuelkeKR WagnerLE StolzC. HubnerT. Riebel2004Myostatin mutation associated with gross muscle hypertrophy in a child.N Engl J Med35026822688
- 4. Wheeler DL, Barrett T, Benson DA, Bryant SH, Canese K, et al. (2008) Database resources of the National Center for Biotechnology Information. Nucleic Acids Res 36: D13–D21.DL WheelerT. BarrettDA BensonSH BryantK. Canese2008Database resources of the National Center for Biotechnology Information.Nucleic Acids Res36D13D21
- 5. Karolchik D, Kuhn RM, Baertsch R, Barber GP, Clawson H, et al. (2008) The UCSC Genome Browser Database: 2008 update. Nucleic Acids Res 36: D773–D779.D. KarolchikRM KuhnR. BaertschGP BarberH. Clawson2008The UCSC Genome Browser Database: 2008 update.Nucleic Acids Res36D773D779
- 6. Safran M, Chalifa-Caspi V, Shmueli O, Olender T, Lapidot M, et al. (2003) Human Gene-Centric Databases at the Weizmann Institute of Science: GeneCards, UDB, CroW 21 and HORDE. Nucleic Acids Res 31: 142–146.M. SafranV. Chalifa-CaspiO. ShmueliT. OlenderM. Lapidot2003Human Gene-Centric Databases at the Weizmann Institute of Science: GeneCards, UDB, CroW 21 and HORDE.Nucleic Acids Res31142146
- 7. Lage K, Karlberg EO, Storling ZM, Olason PI, Pedersen AG, et al. (2007) A human phenome-interactome network of protein complexes implicated in genetic disorders. Nat Biotechnol 25: 309–316.K. LageEO KarlbergZM StorlingPI OlasonAG Pedersen2007A human phenome-interactome network of protein complexes implicated in genetic disorders.Nat Biotechnol25309316
- 8. Aerts S, Lambrechts D, Maity S, Van LP, Coessens B, et al. (2006) Gene prioritization through genomic data fusion. Nat Biotechnol 24: 537–544.S. AertsD. LambrechtsS. MaityLP VanB. Coessens2006Gene prioritization through genomic data fusion.Nat Biotechnol24537544
- 9. Kohler S, Bauer S, Horn D, Robinson PN (2008) Walking the interactome for prioritization of candidate disease genes. Am J Hum Genet 82: 949–958.S. KohlerS. BauerD. HornPN Robinson2008Walking the interactome for prioritization of candidate disease genes.Am J Hum Genet82949958
- 10. van Driel MA, Cuelenaere K, Kemmeren PP, Leunissen JA, Brunner HG, et al. (2005) GeneSeeker: extraction and integration of human disease-related information from web-based genetic databases. Nucleic Acids Res 33: W758–W761.MA van DrielK. CuelenaerePP KemmerenJA LeunissenHG Brunner2005GeneSeeker: extraction and integration of human disease-related information from web-based genetic databases.Nucleic Acids Res33W758W761
- 11. Adie EA, Adams RR, Evans KL, Porteous DJ, Pickard BS (2006) SUSPECTS: enabling fast and effective prioritization of positional candidates. Bioinformatics 22: 773–774.EA AdieRR AdamsKL EvansDJ PorteousBS Pickard2006SUSPECTS: enabling fast and effective prioritization of positional candidates.Bioinformatics22773774
- 12. Adie EA, Adams RR, Evans KL, Porteous DJ, Pickard BS (2005) Speeding disease gene discovery by sequence based candidate prioritization. BMC Bioinformatics 6: 55.EA AdieRR AdamsKL EvansDJ PorteousBS Pickard2005Speeding disease gene discovery by sequence based candidate prioritization.BMC Bioinformatics655
- 13. Oti M, Snel B, Huynen MA, Brunner HG (2006) Predicting disease genes using protein-protein interactions. J Med Genet 43: 691–698.M. OtiB. SnelMA HuynenHG Brunner2006Predicting disease genes using protein-protein interactions.J Med Genet43691698
- 14. Thornblad TA, Elliott KS, Jowett J, Visscher PM (2007) Prioritization of positional candidate genes using multiple web-based software tools. Twin Res Hum Genet 10: 861–870.TA ThornbladKS ElliottJ. JowettPM Visscher2007Prioritization of positional candidate genes using multiple web-based software tools.Twin Res Hum Genet10861870
- 15. Harris MA, Clark J, Ireland A, Lomax J, Ashburner M, et al. (2004) The Gene Ontology (GO) database and informatics resource. Nucleic Acids Res 32: D258–D261.MA HarrisJ. ClarkA. IrelandJ. LomaxM. Ashburner2004The Gene Ontology (GO) database and informatics resource.Nucleic Acids Res32D258D261
- 16. Nakayama J, Arinami T (2006) Molecular genetics of febrile seizures. Epilepsy Res 70: Suppl 1S190–S198.J. NakayamaT. Arinami2006Molecular genetics of febrile seizures.Epilepsy Res70Suppl 1S190S198
- 17. Martin PT (2006) Mechanisms of disease: congenital muscular dystrophies-glycosylation takes center stage. Nat Clin Pract Neurol 2: 222–230.PT Martin2006Mechanisms of disease: congenital muscular dystrophies-glycosylation takes center stage.Nat Clin Pract Neurol2222230
- 18. Smeitink JA, Elpeleg O, Antonicka H, Diepstra H, Saada A, et al. (2006) Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTs. Am J Hum Genet 79: 869–877.JA SmeitinkO. ElpelegH. AntonickaH. DiepstraA. Saada2006Distinct clinical phenotypes associated with a mutation in the mitochondrial translation elongation factor EFTs.Am J Hum Genet79869877
- 19. Coenen MJ, Antonicka H, Ugalde C, Sasarman F, Rossi R, et al. (2004) Mutant mitochondrial elongation factor G1 and combined oxidative phosphorylation deficiency. N Engl J Med 351: 2080–2086.MJ CoenenH. AntonickaC. UgaldeF. SasarmanR. Rossi2004Mutant mitochondrial elongation factor G1 and combined oxidative phosphorylation deficiency.N Engl J Med35120802086
- 20. Kasprzyk A, Keefe D, Smedley D, London D, Spooner W, et al. (2004) EnsMart: a generic system for fast and flexible access to biological data. Genome Res 14: 160–169.A. KasprzykD. KeefeD. SmedleyD. LondonW. Spooner2004EnsMart: a generic system for fast and flexible access to biological data.Genome Res14160169
- 21. Maglott D, Ostell J, Pruitt KD, Tatusova T (2007) Entrez Gene: gene-centered information at NCBI. Nucleic Acids Res 35: D26–D31.D. MaglottJ. OstellKD PruittT. Tatusova2007Entrez Gene: gene-centered information at NCBI.Nucleic Acids Res35D26D31
- 22. Flicek P, Aken BL, Beal K, Ballester B, Caccamo M, et al. (2008) Ensembl 2008. Nucleic Acids Res 36: D707–D714.P. FlicekBL AkenK. BealB. BallesterM. Caccamo2008Ensembl 2008.Nucleic Acids Res36D707D714
- 23. Mitchell JA, Aronson AR, Mork JG, Folk LC, Humphrey SM, et al. (2003) Gene indexing: characterization and analysis of NLM's GeneRIFs. AMIA Annu Symp Proc 460–464.JA MitchellAR AronsonJG MorkLC FolkSM Humphrey2003Gene indexing: characterization and analysis of NLM's GeneRIFs.AMIA Annu Symp Proc460464
- 24. Sherry ST, Ward MH, Kholodov M, Baker J, Phan L, et al. (2001) dbSNP: the NCBI database of genetic variation. Nucleic Acids Res 29: 308–311.ST SherryMH WardM. KholodovJ. BakerL. Phan2001dbSNP: the NCBI database of genetic variation.Nucleic Acids Res29308311
- 25. Calvo S, Jain M, Xie X, Sheth SA, Chang B, et al. (2006) Systematic identification of human mitochondrial disease genes through integrative genomics. Nat Genet 38: 576–582.S. CalvoM. JainX. XieSA ShethB. Chang2006Systematic identification of human mitochondrial disease genes through integrative genomics.Nat Genet38576582
- 26. Guda C, Guda P, Fahy E, Subramaniam S (2004) MITOPRED: a web server for the prediction of mitochondrial proteins. Nucleic Acids Res 32: W372–W374.C. GudaP. GudaE. FahyS. Subramaniam2004MITOPRED: a web server for the prediction of mitochondrial proteins.Nucleic Acids Res32W372W374
- 27. Mulder NJ, Apweiler R, Attwood TK, Bairoch A, Bateman A, et al. (2007) New developments in the InterPro database. Nucleic Acids Res 35: D224–D228.NJ MulderR. ApweilerTK AttwoodA. BairochA. Bateman2007New developments in the InterPro database.Nucleic Acids Res35D224D228
- 28. Finn RD, Tate J, Mistry J, Coggill PC, Sammut SJ, et al. (2008) The Pfam protein families database. Nucleic Acids Res 36: D281–D288.RD FinnJ. TateJ. MistryPC CoggillSJ Sammut2008The Pfam protein families database.Nucleic Acids Res36D281D288
- 29. Kanehisa M, Araki M, Goto S, Hattori M, Hirakawa M, et al. (2008) KEGG for linking genomes to life and the environment. Nucleic Acids Res 36: D480–D484.M. KanehisaM. ArakiS. GotoM. HattoriM. Hirakawa2008KEGG for linking genomes to life and the environment.Nucleic Acids Res36D480D484
- 30. Eppig JT, Blake JA, Bult CJ, Kadin JA, Richardson JE (2007) The mouse genome database (MGD): new features facilitating a model system. Nucleic Acids Res 35: D630–D637.JT EppigJA BlakeCJ BultJA KadinJE Richardson2007The mouse genome database (MGD): new features facilitating a model system.Nucleic Acids Res35D630D637
- 31. Chaurasia G, Iqbal Y, Hanig C, Herzel H, Wanker EE, et al. (2007) UniHI: an entry gate to the human protein interactome. Nucleic Acids Res 35: D590–D594.G. ChaurasiaY. IqbalC. HanigH. HerzelEE Wanker2007UniHI: an entry gate to the human protein interactome.Nucleic Acids Res35D590D594
- 32. Su AI, Wiltshire T, Batalov S, Lapp H, Ching KA, et al. (2004) A gene atlas of the mouse and human protein-encoding transcriptomes. Proc Natl Acad Sci U S A 101: 6062–6067.AI SuT. WiltshireS. BatalovH. LappKA Ching2004A gene atlas of the mouse and human protein-encoding transcriptomes.Proc Natl Acad Sci U S A10160626067
- 33. Boeckmann B, Bairoch A, Apweiler R, Blatter MC, Estreicher A, et al. (2003) The SWISS-PROT protein knowledgebase and its supplement TrEMBL in 2003. Nucleic Acids Res 31: 365–370.B. BoeckmannA. BairochR. ApweilerMC BlatterA. Estreicher2003The SWISS-PROT protein knowledgebase and its supplement TrEMBL in 2003.Nucleic Acids Res31365370