Neurocarta: aggregating and sharing disease-gene relations for the neurosciences
© Portales-Casamar et al; licensee BioMed Central Ltd. 2013
Received: 31 July 2012
Accepted: 23 February 2013
Published: 26 February 2013
Understanding the genetic basis of diseases is key to the development of better diagnoses and treatments. Unfortunately, only a small fraction of the existing data linking genes to phenotypes is available through online public resources and, when available, it is scattered across multiple access tools.
Neurocarta is a knowledgebase that consolidates information on genes and phenotypes across multiple resources and allows tracking and exploring of the associations. The system enables automatic and manual curation of evidence supporting each association, as well as user-enabled entry of their own annotations. Phenotypes are recorded using controlled vocabularies such as the Disease Ontology to facilitate computational inference and linking to external data sources. The gene-to-phenotype associations are filtered by stringent criteria to focus on the annotations most likely to be relevant. Neurocarta is constantly growing and currently holds more than 30,000 lines of evidence linking over 7,000 genes to 2,000 different phenotypes.
Neurocarta is a one-stop shop for researchers looking for candidate genes for any disorder of interest. In Neurocarta, they can review the evidence linking genes to phenotypes and filter out the evidence they’re not interested in. In addition, researchers can enter their own annotations from their experiments and analyze them in the context of existing public annotations. Neurocarta’s in-depth annotation of neurodevelopmental disorders makes it a unique resource for neuroscientists working on brain development.
KeywordsPhenotype Genes Knowledgebase Brain development
There is a tremendous amount of research focusing on understanding the genetic basis of disease. Studies use a wide range of strategies, including targeted gene approaches, genome-wide screens, and animal models. As such studies continue to proliferate and provide insights on specific disorders, it is important to integrate the information in order to make the best use of the data and increase the level of insight that can be gained from new studies. Knowledge that crosses studies and disorders can be used to perform meta-analyses, to uncover commonalities among conditions, and to tease apart the factors that contribute to phenotypes that make up a disorder. However, currently, information about the genetic and molecular basis of diseases is distributed among a range of specialized or generic data resources, hindering its optimal use . Examples of more or less generic databases are Online Mendelian Inheritance in Man (OMIM) , the Rat Genome Database (RGD) , and the Comparative Toxicogenomics Database (CTD) . While these different resources overlap in their disease coverage and data sources, they are also complementary in that each of the curation teams making the annotations has different criteria for inclusion and different biases. Other databases are dedicated to specific disorders, these include the Simons Foundation Autism Research Initiative Gene Database (SFARI Gene) for autism , PDGene for Parkinson’s disease , Alzgene for Alzheimer’s disease , MSGene for multiple sclerosis , ADHDgene for Attention Deficit Hyperactivity Disorder , and CADgene for Coronary Artery Disease .
The resource we describe was motivated by the establishment of a large Canadian research network “NeuroDevNet”, with the goal of translating knowledge into improved diagnosis, prevention and treatment of neurodevelopmental disorders [11, 12]. To facilitate the design and interpretation of genetics studies, we recognized the need for a resource that captures existing information, but none of the resources mentioned above was sufficiently comprehensive. This was in part because genetic investigations of two of the disorders of interest to NeuroDevNet, Fetal Alcohol Spectrum Disorder (FASD) and Cerebral Palsy (CP) were not well covered by any existing database.
Neurocarta is an online resource focusing on the genetic basis of neurodevelopmental disorders. In addition to containing manually curated information on disorders of interest to neurodevelopmental researcher, Neurocarta aggregates data from multiple disease gene resources so that the neurodevelopmental annotations can be examined in the context of other disease annotations, providing a better understanding of how generic the function of the gene might be.
Construction and content
Database schema and implementation
Neurocarta benefits from the registration system implemented in Gemma  allowing users the option of registering and entering their own annotations. The annotations can be set to be either public or private. When private, the owner can decide whom to share them with, using a group-based authorization framework.
Top ten genes with the most associated phenotypes
# of phenotypes
tumor necrosis factor
prostaglandin-endoperoxide synthase 2
matrix metallopeptidase 9
phosphatase and tensin homolog
major histocompatibility complex, class II, DR beta 1
interleukin 1, beta
tumor protein p53
transforming growth factor, beta 1
Top ten phenotypes with the most associated genes
# of genes
autism spectrum disorder
type 2 diabetes mellitus
peripheral nervous system disease
Data extraction from external sources
We have defined stringent criteria for automatic inclusion of data from external sources, with the goal of limiting the inclusion of unreliable data or information that we deem of limited utility to our target audience. In this section we provide details of procedures for each resource. As we are continuing to add resources to the system, information on the inclusion criteria and import procedures is also maintained on the Neurocarta website at http://gemma-doc.chibi.ubc.ca/neurocarta/data-sources.
OMIM : The OMIM data files (morbidmap.txt and mim2gene.txt) are downloaded from the OMIM FTP site. We extract unique mappings between Phenotype MIM numbers and Gene MIM numbers from morbidmap.txt and map the genes to their NCBI identifiers in mim2gene.txt.
RGD : The RGD Gene-Disease association files (homo_genes_rdo, mus_genes_rdo, rattus_genes_rdo) are downloaded from the RGD FTP site. Annotations with the following evidence codes are ignored: ISS (redundant across species), NAS (non-traceable author’s statements are debatable), and IEA (electronic annotations come from other sources, GAD for example) and we prefer to get these annotations directly from the source). Annotations without a PubMed reference are ignored as well.
CTD : The CTD Gene-Disease association file (CTD_genes_diseases.tsv) is downloaded from the CTD website. We only consider curated annotations with Direct Evidence set to “marker/mechanism” or “therapeutic”, and at least one PubMed reference.
Disease-specific databases: The SFARI  annotation files (autism-gene-dataset.csv, gene-score.csv) are downloaded form the SFARI Gene website. Each PubMed reference is imported as separate literature evidence in Neurocarta, with the option of it being defined as “negative” whenever specified in the annotation file. The PDGene , AlzGene , and MSGene  “Top Results” are extracted from their respective websites. All three databases assess their results for their epidemiological credibility using two methods: (1) The HuGENet interim criteria for the cumulative assessment of genetic associations [20, 21], and (2) Bayesian analyses [22, 23]. Only meta-analysis results with P-values <0.00001 are considered. The “Hot gene list” from ADHDgene  is extracted from their website. This list includes all genes that have been identified in at least five independent studies. The ALSoD  top 20 genes are identified through the credibility score analysis provided on their website. The genes are ranked by the number of affected patients and by the number of mutations per gene, and the ranks are summed to determine the final rank for each gene. For the IDGene  and EpiGAD  databases, we wanted to extract more information than what was readily accessible through respective websites. We manually reviewed the genes listed in each database and used that information as a seed for targeted PubMed searches and manual curation of relevant publications.
Disease mapping from external sources to Disease Ontology (DO) terminology
For the disorder-specific databases we use the corresponding appropriate terms in DO (e.g., “autism spectrum disorder” for SFARI and “amyotrophic lateral sclerosis” for ALSoD). As described next, for other databases we used a combination of automatic and semi-automatic methods for mapping.
OMIM, RGD, and CTD: These three resources provide OMIM or MeSH terms that we mapped to DO terms as follows. First, we use the Xref mappings provided in the Human_DO.obo ontology file, which covers about 50% of the phenotype-gene mappings in these resources. For the remaining that use terms lacking a DO Xref, we use the NCBO Annotator Web service  followed by manual quality control to resolve partial matches, increasing coverage substantially. In total about 2/3 of the phenotype-gene associations present in OMIM, RGD, or CTD could be mapped to a DO term. This is due to non-disease terms that are listed in OMIM but not in DO (e.g., “Blood type”, “Ig levels”), and some disease terms missing from DO (mostly syndromic, e.g., TARP syndrome, Jawad syndrome), or missed mappings. We have notified the DO maintainers of these gaps and expect to eventually be able to import a greater fraction of these annotations into Neurocarta.
Manual curation of the literature
While the Neurocarta framework is generic, our curation team is focusing on annotations relevant to our primary research interest, neurodevelopmental disorders. In-depth annotations have been produced on the following Disease Ontology terms (including respective children terms): (i) “Autism Spectrum Disorder” (ASD; DOID_0060041); (ii) “Cerebral Palsy” (CP; DOID_1969); (iii) “Fetal Alcohol Spectrum Disorder” (FASD; DOID_0050696); (iv) “Epilepsy” (DOID_1826); and (v) and “Intellectual disability” (DOID_1059). When necessary, phenotype descriptions were complemented with more descriptive Human or Mammalian Phenotype Ontology terms such as “Memory impairment” (HP_0002354), “EEG abnormality” (HP_0002353), or “decreased brain size” (MP_0000774). Curators review the literature using PubMed searches across all fields (that is, the default PubMed setting) using queries such as “epilepsy” AND “genetics”. We avoid making searches that are gene-centric, except as a secondary mechanism to find additional citations on a gene-phenotype relationship identified through initial screening. When possible, review papers are used to identify primary research papers, which are then curated as “Experimental Type Evidence”. The curators record details about the experiment using controlled vocabularies, categorized as (for example) “Bio Source”, “Experiment Design”, or “Developmental Stage”. The criterion for inclusion is an experimentally-supported statement linking the gene to the phenotype. The exception is genome-wide studies where the results were not yet confirmed by follow-up experiments. The curated papers involve a wide variety of experiments including both animal models and human studies. For the former, if the authors describe the animal model as a specific model for the disorder of interest, the curators associate the gene studied in the paper directly to the human disease. If the authors describe an endophenotype that is related to the disease, the gene is associated to the endophenotype only. In some cases, review papers are used as the source of the annotations instead of drilling down to the original research papers. In that case, it is curated as “Literature Type Evidence” with no details about the experiments. To help users navigate through the evidence, we are, when possible, associating phenotypes to genes in a species-specific way. So, for instance, if the evidence comes from an experiment done in rats, it will be linked in Neurocarta to the rat gene.
Utility and discussion
Neurocarta was originally conceived to help researchers identify candidate genes that might be involved in their disorder of interest, based on existing knowledge, and put that information in the context of other phenotypes associated with the genes. Neurocarta allows users to extract the list of genes that have been associated to a specific disorder, look at the detail of the evidence, and apply further selection criteria. It can also be used to identify relevant literature pertaining to a gene or phenotype of interest. By aggregating data from multiple sources, we enable a global view of each gene’s involvement in diseases, facilitating the identification of genes specifically involved in one disorder versus genes involved in many disease processes. Such candidate gene lists can be used by researchers who perform genome-wide studies, helping them identifying the most likely candidates in their results. It can also inform more targeted approaches as to which gene to include in the study. Another unique aspect of Neurocarta is the ability that users have to enter their own annotations. This enables them to share unpublished results with collaborators as well as put their findings in the context of existing data and facilitate interpretation.
Investigating gene-to-phenotype associations for neurodevelopmental disorders
Genes in Neurocarta associated with neurodevelopmental disorders
# of specific genes
% of specific genes
Comparison to similar existing resources
Several genotype to phenotype databases have been created with the idea of aggregating data from several sources in a common standardized online tool . Some of existing tools rely entirely on OMIM annotations and only provide a more sophisticated portal to access data [29–31]. Others automatically aggregate data from a collection of resources, including OMIM, but they either focus only on human annotations , or on only one major phenotype database for a selection of model organisms . Finally, some of the tools have been designed for human genetic association studies only and aggregate data from automatic or curated review of the literature [34–37]. Neurocarta is unique compared to these various initiatives in that it aggregates data from different organisms (human and animal models of diseases) and different kinds of studies (from genetic association to basic molecular experiments). It puts side-by-side data automatically extracted from public resources as well as manually curated from selected papers in the literature. All data goes through a review process where only the most reliable annotations are kept to reduce noise in the system. Finally, Neurocarta is the only publicly-available online tool that allows users to enter their own genotype to phenotype associations, share them with other users, and analyze them in the context of all existing annotations.
We are planning several lines of improvements to Neurocarta’s data and software layers. Neurocarta currently includes very few data from genome-wide association studies because of the high rate of false positives that can arise from these data. We have included data from PDGene, AlzGene, and MSGene but only the top results that reached significance in their meta-analyses of the data. In the case of ADHDgene, we have decided to incorporate their Hot Gene list even though it was only based on the number of studies a gene was identified in. We are currently investigating different options to incorporate the most significant results from additional genetic association data from public resources such as GAD , GWASdb , or the GWAS catalog . Another development that we feel will add value to Neurocarta is to incorporate automated Gemma differential expression analysis results. Neurocarta is part of Gemma but currently does not take a full advantage of this integration. In Gemma, gene expression datasets comparing control vs. disease cases are tagged and easily identifiable. We will apply differential expression analysis to these datasets using stringent thresholds to identify genes differentially expressed in specific diseases. We will then incorporate this analysis result as a new type of evidence linking genes to phenotypes in Neurocarta. Finally, a challenge in making the best use of the data is that different sources have different levels of evidence quality associated with them. For example, human geneticists would generally rate evidence from animal models as weak. Neurocarta does not directly capture such distinctions, so we are in the process of devising an evidence-rating scheme that will be used to automatically rank genes with respect to their strength of evidence in association with each disorder.
Neurocarta is a new online resource linking genes to phenotypes. It brings together data from a wide variety of public resources and from manual curation of the literature. It is unique in that it allows users to enter their own annotations and keep them private if they wish to. In-depth annotations of genes involved in brain development disorders are available but Neurocarta is not restricted to a single disease. Instead, Neurocarta enables users to visualize all diseases their gene of interest might be associated with. This allows users not only to extract candidate gene lists from the system, but also to identify which of these genes are the most specific to their disorder of interest and to quickly find papers supporting these associations. Our analysis of the data in the context of neurodevelopmental disorders demonstrates that existing annotations linking genes to phenotypes are skewed to genes that are well known and involved in many biological functions. Neurocarta exposes this problem and makes it easier for researchers to focus their attention on more “specific” genes.
Availability and requirements
Neurocarta is publicly available at http://neurocarta.chibi.ubc.ca.
Attention deficit hyperactivity disorder gene database
Alzheimer’s disease gene database
Autism spectrum disorder
Comparative toxicogenomics database
Fetal alcohol spectrum disorder
Genetic association database
Genome-wide association study database
Inferred from electronic annotation
Inferred from sequence or structural similarity
Multiple sclerosis gene database
Non-traceable author statement
National Center for Biotechnology Information
Online mendelian inheritance in man
Parkinson’s disease gene database
Rat genome database
Simons Foundation Autism Research Initiative.
This work was supported by the NeuroDevNet Network of Centres of Excellence (Neuroinformatics Core and Opportunities Initiatives grants to PP) and NIH grant RO1-GM076990 to PP. We thank Sanja Rogic for comments on the manuscript, Thea Van Rossum for software and graphics contributions, James Reynolds, Michael Shevell, Lonnie Zwaigenbaum, Steven Scherer, and Marie-Pierre Dubé for advice and encouragement.
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