Visual annotation display (VLAD): a tool for finding functional themes in lists of genes
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Experiments that employ genome scale technology platforms frequently result in lists of tens to thousands of genes with potential significance to a specific biological process or disease. Searching for biologically relevant connections among the genes or gene products in these lists is a common data analysis task. We have implemented a software application for uncovering functional themes in sets of genes based on their annotations to bio-ontologies, such as the gene ontology and the mammalian phenotype ontology. The application, called VisuaL Annotation Display (VLAD), performs a statistical analysis to test for the enrichment of ontology terms in a set of genes submitted by a researcher. The results for each analysis using VLAD includes a table of ontology terms, sorted in decreasing order of significance. Each row contains the term, statistics such as the number of annotated terms, the p value, etc., and the symbols of annotated genes. An accompanying graphical display shows portions of the ontology hierarchy, where node sizes are scaled based on p values. Although numerous ontology term enrichment programs already exist, VLAD is unique in that it allows users to upload their own annotation files and ontologies for customized term enrichment analyses, supports the analysis of multiple gene sets at once, provides interfaces to customize graphical output, and is tightly integrated with functional and biological details about mouse genes in the Mouse Genome Informatics (MGI) database. VLAD is available as a web-based application from the MGI web site (http://proto.informatics.jax.org/prototypes/vlad/).
KeywordsGene Ontology Term Enrichment Mouse Genome Informatics Mammalian Phenotype VisuaL Annotation
One of the challenges facing biologists in the era of genome scale science is to glean biological meaning from large experimental datasets such as those generated by microarray, RNA Seq, ChIP (chromatin immunoprecipitation) Seq, genome wide copy number variation (CNV) analysis, and exome sequencing. The development of biomedical ontologies such as the Gene Ontology (GO) (Ashburner et al. 2000; Gene Ontology 2015) and annotated gene sets (Subramanian et al. 2005) have been essential for mining functional properties of genes from large-scale datasets.
Numerous software tools that use curated annotations and ontologies for extracting functional information from gene sets have been developed over the years including GO::TermFinder (Boyle et al. 2004), DAVID (da Huang et al. 2009), BiNGO (Maere et al. 2005), AmiGO (Carbon et al. 2009), GoMiner (Zeeberg et al. 2003), and WebGestalt (Wang et al. 2013). In general, these programs are designed to analyze gene sets that show statistically significant patterns of gene expression, variation, etc. Other gene set analysis methods such as gene set enrichment analysis (GSEA) (Subramanian et al. 2005), parametric analysis of gene set enrichment (PAGE) (Kim and Volsky 2005), and generally applicable gene set enrichment (GAGE) (Luo et al. 2009) allow for the analysis of all genes in global transcriptomics studies. These methods were developed to address the issue that not all meaningful gene expression changes rise to the level of statistical significance. Both the “cutoff -based” and “cutoff-free” methods (Luo et al. 2009) rely on comparisons of experimental gene sets to annotated gene sets and ontologies to facilitate data interpretation.
We describe here a web-based application called VLAD (VisuaL Annotation Display) for finding functional themes in sets of genes based on their ontology term annotations. VLAD uses the hypergeometric test for determining significance and is appropriate for the analysis of gene sets that are generated by “cutoff-based” statistical analyses methods. VLAD is highly configurable; there are many parameters that can be set by users that control input, data processing, and output. A unique feature of the software relative to existing term enrichment tools is that it is not limited to the two native ontologies in the system: the Gene Ontology (Ashburner et al. 2000) and the Mammalian Phenotype Ontology (Smith and Eppig 2012); rather, VLAD can compare lists of genes to any structured vocabulary that is in the standard open biological and biomedical ontologies (OBO) format (http://www.obofoundry.org) (Smith et al. 2007) and for which there is a file of gene-to-annotation-term associations in the GO Annotation Format (GAF; http://geneontology.org/page/go-annotation-file-gaf-format-10). VLAD also provides users with a level of control over the graphical display of results that is not available in other similar analysis sites. VLAD is available as a web-based application from the Mouse Genome Informatics (MGI) web site (http://proto.informatics.jax.org/prototypes/vlad/).
Materials and methods
To illustrate the functionality of VLAD, we analyzed genes from a previously published study that described the genome wide gene expression patterns across key developmental stages of normal mouse diaphragm (Russell et al. 2012). In this study, the investigators used time-series analysis (Ernst and Bar-Joseph 2006) of microarray-based expression data to identify over 650 genes whose expression levels increased significantly between embryonic day 11.5 and embryonic day 16.5 and over 360 genes whose expression levels decreased significantly over this same time period.
To demonstrate the extensibility of VLAD to user-provided ontologies, an OBO ontology of mouse biochemical pathways (mousecyc_obo.txt) and a corresponding set of annotations in GAF format (mousecyc_gaf.txt) from the curated MouseCyc database (Evsikov et al. 2009) were downloaded from the MouseCyc project ftp site (ftp://informatics.jax.org/pub/curatorwork/MouseCycDB/) and chosen as the basis for a custom term enrichment analysis using the Annotation Data Set options on the VLAD homepage. The mouse diaphragm gene lists, OBO ontology, and GAF files are available as supplemental data and from the following ftp site: ftp://informatics.jax.org/pub/supplemental/MammGenome2015.
VLAD is preconfigured to work with either gene-function annotations from MGI using the GO and/or gene-phenotype annotations from MGI using the Mammalian Phenotype (MP) Ontology. The GO and MP annotations used by VLAD are updated weekly. A user may also upload a different ontology (a file in OBO format) and corresponding annotation dataset (a file in GAF format) to perform custom enrichments. Users may also use the built in MP and GO ontologies but supply their own gene-to-ontology term annotations.
To run an analysis with VLAD users submit one or more test sets of gene symbols or accession identifiers for the laboratory mouse. By default, the test set of genes is compared to the annotations for all genes in the mouse reference genome to determine the likelihood that the annotation terms associated with the test set would occur by chance. Alternatively, users can submit a custom list of genes to which their test set should be compared. This option may be preferable for the analysis of lists of genes from studies that use a targeted set of genes for analysis; the distribution of annotations for genes for such targeted studies may be quite different than the annotations for the genome as a whole. Annotations from all sources of evidence are included in the analysis by default. The user has the option of limiting the analysis to only those annotations derived from specific classes of evidence. For example, it may be desirable to limit analyses to only those annotations derived from direct experimental assays as opposed to those inferred from sequence similarity or homology. For custom enrichment analyses, users can include their own evidence codes in the input GAF file. These user-supplied codes can be specified in the evidence code parameter settings of VLAD to exclude specific sets of annotations from the enrichment analysis.
A unique feature of VLAD is the support for the analysis of multiple gene sets at a time. For example, the up-regulated and down-regulated gene sets from a transcriptomics experiment can be analyzed at the same time to evaluate the biological consequence of gene expression changes from the perspective of biological function. Each gene set is analyzed independently, and the results are shown in a combined display designed to reveal enrichment differences between the sets.
Calculating statistical significance of annotations for a gene set
Suppose out of a list of 100 genes up-regulated in a disease sample relative to normal, 40 are associated with mortality/aging phenotypes. Is 40 % significant? What would we expect to see if we simply picked 100 genes at random? Like many other ontology term enrichment tools, VLAD calculates significance based on the hypergeometric distribution. For every term, t, in the ontology, VLAD computes a p value, p t (k, n, K, N), where k is the number of genes in the query set annotated to t or its descendants, n is the size of the query set, K is the total number of genes in the database annotated to t or its descendants, and N is the total number of annotated genes. The results are sorted with the terms of highest significance at the top. The default analysis in VLAD is for term enrichment where the p value is the probability of drawing at least k successes in n tries given a population of K out of N. VLAD also offers the option of performing a depletion analysis where p is the probability of drawing at most k successes in n tries.
One issue that VLAD and similar tools must deal with is the multiple testing problem (Noble 2009), which in this case means that the reported p values are inflated simply because we are calculating them for so many terms (i.e., doing many tests). To account for multiple testing in VLAD an additional statistic, the q value is calculated, which is based on the concept of the positive false discovery rate (pFDR) (Storey 2002). The q value is the proportion of false positives when a given group of tests is called significant and is easily computed from the ordered p values. In terms of the results generated by VLAD, the q value in row i, q i, is interpreted as the rate of false positives if we were to consider all terms in rows 0…i to be significant.
The output from the VLAD program includes both graphical and tabular representations of the ontology terms associated with the user-supplied gene list (i.e., the query set) and the calculated significance scores. The tabular display shows the detailed results, i.e., all the ontology terms, their scores, statistics, and associated genes, sorted in order of decreasing significance. The graphical display provides a high level visual summary of the most significant terms from table. Each node in the graph corresponds to a term and node sizes are scaled by term significance. VLAD uses GraphViz (Gansner and North 1999) (http://www.graphviz.org/) for graph layout and visualization. The nodes in the graph and the rows in the tabular view are cross-linked so the user can easily move between the two kinds of display. The results of a gene set analyses in VLAD can be downloaded and saved to a user’s local disk. VLAD also provides the option of downloading results as an Excel spreadsheet or tab-delimited file.
VLAD provides numerous options allowing the user to customize color, image size, and nodes to display. Even for small sets of genes, the number of associated ontology terms, and hence, the size of the resulting image, may be large. VLAD provides adjustable parameters that allow the user to limit the number and reduce the size of the nodes drawn in the image. The “limit nodes” option allows the user to display only those nodes that meet specific scoring criteria. The “cull interior nodes” option allows the user to further reduce the size of the graphic by omitting many uninformative interior nodes from the display. This option is “on” by default. The root node in the ontology is always included regardless of the settings because it is visually important and helps establish context for the user.
The lists of up- and down-regulated genes from a published mouse diaphragm development study (Russell et al. 2012) were analyzed for term enrichment for both the gene ontology and Mammalian Phenotype Ontology using VLAD. The graphical output for both of these analyses is shown in Fig. 1a, b. The results of the VLAD analysis demonstrate that the genes that decline over time during diaphragm development are primarily involved with general mammalian organogenesis and systems development, while genes that increase are associated with muscle development and contractility (Fig. 1a). Likewise, the down-regulated genes are enriched in phenotypes associated with abnormal survival, while the up-regulated gene set is associated with abnormal muscle phenotypes (Fig. 1b). The option in VLAD to display the enrichment results for both sets of genes simultaneously helps to highlight the biological and functional differences represented in the two sets of genes.
VLAD is a highly configurable web-based exploratory data analysis tool for the term enrichment analysis. Compared to web-based software tools with comparable functionality, VLAD is unique in the degree to which it can be adapted easily to use any ontology and annotation combination. In its current implementation, VLAD is designed to work best for term enrichment/depletion analysis for the laboratory mouse. Planned enhancements to the software will include support for more species, specifically for human gene sets. Future versions of VLAD will include additional algorithms for term enrichment (e.g., (Bauer et al. 2010; Glass and Girvan 2014; Prufer et al. 2007) and allow users to share ontology and annotation files they use for custom term enrichment analyses.
VLAD is available as a web-based application from the Mouse Genome Informatics (MGI) web site at the following URL: http://proto.informatics.jax.org/prototypes/vlad/. User documentation for VLAD is provided online from the VLAD home page.
The authors thank Drs. Gary Churchill and Matthew Hibbs for helpful discussions regarding the calculation of statistical significance using the hypergeometric distribution. Special thanks to Dr. John Eppig, whose interest in using VLAD contributed greatly to its development. The authors thank the anonymous reviewers for their thoughtful critiques. The development and implementation of VLAD was supported, in part, by NIH HG00330-P1.
- Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, Cherry JM, Davis AP, Dolinski K, Dwight SS, Eppig JT, Harris MA, Hill DP, Issel-Tarver L, Kasarskis A, Lewis S, Matese JC, Richardson JE, Ringwald M, Rubin GM, Sherlock G (2000) Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet 25:25–29PubMedCentralCrossRefPubMedGoogle Scholar
- Boyle EI, Weng S, Gollub J, Jin H, Botstein D, Cherry JM, Sherlock G (2004) GO:termFinder–open source software for accessing Gene Ontology information and finding significantly enriched Gene Ontology terms associated with a list of genes. Bioinformatics 20:3710–3715PubMedCentralCrossRefPubMedGoogle Scholar
- Gansner E, North S (1999) An open graph visualization system and its applications to software engineering. Softw Pract Exp S1:1–5Google Scholar
- Smith B, Ashburner M, Rosse C, Bard J, Bug W, Ceusters W, Goldberg LJ, Eilbeck K, Ireland A, Mungall CJ, Consortium OBI, Leontis N, Rocca-Serra P, Ruttenberg A, Sansone SA, Scheuermann RH, Shah N, Whetzel PL, Lewis S (2007) The OBO Foundry: coordinated evolution of ontologies to support biomedical data integration. Nature Biotechnol 25:1251–1255CrossRefGoogle Scholar
- Subramanian A, Tamayo P, Mootha VK, Mukherjee S, Ebert BL, Gillette MA, Paulovich A, Pomeroy SL, Golub TR, Lander ES, Mesirov JP (2005) Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profiles. Proc Natl Acad Sci USA 102:15545–15550PubMedCentralCrossRefPubMedGoogle Scholar
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