- Open Access
Disjunctive shared information between ontology concepts: application to Gene Ontology
© Couto and Mário; licensee BioMed Central Ltd. 2011
- Received: 26 April 2011
- Accepted: 31 August 2011
- Published: 31 August 2011
The large-scale effort in developing, maintaining and making biomedical ontologies available motivates the application of similarity measures to compare ontology concepts or, by extension, the entities described therein. A common approach, known as semantic similarity, compares ontology concepts through the information content they share in the ontology. However, different disjunctive ancestors in the ontology are frequently neglected, or not properly explored, by semantic similarity measures.
This paper proposes a novel method, dubbed DiShIn, that effectively exploits the multiple inheritance relationships present in many biomedical ontologies. DiShIn calculates the shared information content of two ontology concepts, based on the information content of the disjunctive common ancestors of the concepts being compared. DiShIn identifies these disjunctive ancestors through the number of distinct paths from the concepts to their common ancestors.
DiShIn was applied to Gene Ontology and its performance was evaluated against state-of-the-art measures using CESSM, a publicly available evaluation platform of protein similarity measures. By modifying the way traditional semantic similarity measures calculate the shared information content, DiShIn was able to obtain a statistically significant higher correlation between semantic and sequence similarity. Moreover, the incorporation of DiShIn in existing applications that exploit multiple inheritance would reduce their execution time.
- Gene Ontology
- Direct Acyclic Graph
- Semantic Similarity
- Protein Pair
- Ontology Concept
Comparison techniques have always been essential tools for managing knowledge. For example, the study and analysis of a given protein often starts by comparing it with related proteins, and that characterization can be helpful to better understand it. However, the number of possible proteins that can be compared is huge and does not stop growing, due to contemporary high-throughput technologies. Thus, the quest for efficient advanced computational sequence comparison techniques to search for similar proteins is omnipresent in many fields of proteomics.
The most straightforward comparison methods are sequence-based. They only require information on their internal structure (the sequence itself), but limit the analysis to proteins sharing a similar structure, independently of their biological role. This ignores ontological knowledge about the properties and relationships among proteins. For example, when looking for proteins with an oxidoreductase activity, we may be not only interested in proteins annotated with this activity, but also other similar activities, such as monooxygenase activity, independently on how structurally similar the proteins are. Thus, in opposition or as a complement to structural similarity, we should also attempt to compare proteins based on the relationships between them .
This has motivated the development of ontology-based similarity measures in the past , defining similarity between concepts as a combination of the measures of their common and distinctive relationships, inspired on Tversky's contrast model . Ontology-based similarity has become a prominent approach to compare biomedical entities based on their biomedical activity. Many similarity measures have been applied to biomedical ontologies, and compared against traditional structural similarity measures [4–8]. In the biomedical field, ontology-based similarity measures are normally referred to as semantic similarity measures, contrasting with structural similarity measures, and thus this paper also adopts that nomenclature.
Measures based on the information content that two concepts share were the first to identify a correlation between protein sequence similarity and semantic similarity . More recently, the notion of shared information content has been applied to semantically compare diseases, phenotypes and chemical compounds [10–12]. Most ontologies represent relationships between their concepts as Directed Acyclic Graphs (DAG). Thus, the shared information between two concepts is normally proportional to the information content of the Most Informative Common Ancestor (MICA) in the DAG, and the Information Content (IC) of a concept is inversely proportional to its frequency in a given corpus. The frequency of a concept is also propagated to its ancestors, making the IC of a concept related to its depth in the DAG. When entity mappings are available, frequency is normally defined as the number of entities mapped to each concept, normally referred to as annotations.
Using only the MICA to define similarity equates to considering the DAG as a tree, i.e. neglecting the multiple inheritance nature of the DAG. This problem was identified by Resnik, who decided to use only one of the possibilities for each concept . The decision is consistent with previous treatments of disjunctive concepts , where they define the distance between two disjunctive sets of concepts as the minimum path length from any element of the first set to any element of the second. Despite the value of this approach in natural language processing applications, in other domains, such as the Life Sciences, similarity measures are expected to account for the multi-faceted nature of their concepts and entities. The exploitation of multiple inheritance was previously addressed by GraSM, where the shared information content between two concepts is re-defined as the average of all their disjunctive ancestors . GraSM assumes that two common ancestors are disjunctive if there are independent paths from both ancestors to each concept. The implementation of GraSM is rather complex, and it lowers the similarity of concepts that share parallel interpretations instead of raising it, as this represents a stronger relation between concepts sharing more independent information. Taking the example in Figure 1, GraSM considers platinum and palladium more similar than platinum and gold, since gold can have a different interpretation (coinage). However, we could also expect that silver and gold to be more similar than platinum and gold or platinum and palladium, since silver and gold share two parallel interpretations, precious and coinage. GraSM considers the opposite, since silver and gold have two interpretations, it reduces their similarity, which is counterintuitive.
To overcome the problems described above, this paper proposes a novel method for calculating the shared information content between two concepts, dubbed Disjunctive Shared Information (DiShIn), based on the number of distinct paths between the concepts and their common ancestors. Like GraSM, DiShIn re-defines the shared information content between two concepts as the average of all their disjunctive ancestors. However, DiShIn assumes that an ancestor is disjunctive if the difference between the number of distinct paths from the concepts to it is different from that of any other more informative ancestor. In other words, a disjunctive ancestor is the most informative ancestor representing a given set of parallel interpretations. Like GraSM, DiShIn can be directly integrated into any semantic similarity measure based on the MICA. Taking again the example of Figure 1, DiShIn still considers platinum and palladium more similar than platinum and gold. This happens because the number of distinct paths from both platinum and palladium to precious and metal is one. Therefore, only precious is considered to be a disjunctive ancestor. On the other hand, the number of distinct paths from both platinum and gold to precious is one but from gold to metal is two. Therefore, both precious and metal are considered to be disjunctive ancestors. Since the shared information is defined as the average of the disjunctive ancestors and the IC of metal is smaller than precious, then the similarity between platinum and palladium is higher than platinum and gold. However, unlike GraSM, DiShIn does not consider silver and gold less similar than platinum and gold or platinum and palladium. This happens because the number of distinct paths from both silver and gold to precious and coinage is one and to metal is two. All ancestors have the same number of distinct paths from each concept, thus only precious or coinage will be considered a disjunctive ancestor, depending of which has the highest IC. This means that the similarity between silver and gold will be higher than platinum and gold and at least equal to platinum and palladium.
We applied DiShIn to one of most popular ontologies in the biomedical domain, the Gene Ontology. The performance of DiShIn was evaluated using CESSM, an existing platform for collaborative and automated evaluation of protein similarity measures . For a pre-defined list of pairs of proteins, CESSM calculates the correlation coefficients between semantic and sequence similarity. Sequence similarity is considered here the golden standard, following the common assumption that entities that are globally similar in structure tend to have similar biological activity . DiShIn was able to obtain statistically significant higher correlation coefficients than GraSM and MICA alone.
Thus, the main contributions of this paper are:
formalization of a novel method, DiShIn, to calculate shared information content using multiple inheritance (Methods Section);
application of DiShIn to Gene Ontology (Gene Ontology Application Section);
evaluation of DiShIn performance against state-of-the-art methods (Results and Discussion Section).
This section presents the current approaches to define similarity between ontology concepts as a combination of their common and distinctive relationships in the ontology.
where Paths(a, c) gives the set of distinct paths from c to a in the DAG.
In the case where IC(precious) < IC(coinage) we will have the opposite, but Share grasm (silver, gold) will still be penalized against any other pair of concepts that only share coinage.
where Paths gives the number of distinct paths from c to a in the DAG.
To illustrate how DiShIn handles parallel interpretations differently from GraSM, this section presents the application of DiShIn to the case of multiple inheritance of Figure 1.
This shows that, unlike GraSM, DiShIn does not penalize pairs of concepts with parallel interpretations, and, like GraSM, it penalizes pairs of concepts with distinct paths for the same interpretation.
Before using DiShIn, we need to estimate the IC for each concept, and calculate the number of distinct paths from one concept to another, Paths(c1, c2). These preliminary calculations depend on the used ontology and on the available annotations. In the worst-case scenario, we need to use an all-pairs shortest paths algorithm to calculate Paths(c1, c2) and propagate the frequency of concepts to obtain their IC, so we can estimate a computational complexity of for these preliminary calculations, where n is the number of ontology concepts . However, the calculations only need to be performed once, and updated as new versions of the ontology become available. Thus, the time spent on these calculations has no impact on the performance of DiShIn.
After calculating the IC(c) and Paths(c1, c2), let's assume that we store their information in a relational database as two tables, IC and Paths, respectively. The table IC is composed of two columns, holding the concept identifier and a value representing the information content of the concept. The table Paths is composed of three columns, holding a concept identifier, another concept identifier representing an ancestor of the former concept, and a value representing the number of paths between the two concepts. Thus, with these two tables DiShIn could be implemented as a single SQL query:
SELECT AVG(DCA. value)
(SELECT MAX(IC. value) as value
(SELECT p1. ancestor as ancestor,
ABS (p1. value - p2. value)
FROM Paths p1, Paths p2
WHERE p1. concept = c1
AND p2. concept = c2
AND p1. ancestor = p2. ancestor
AND p1. value > 0 AND p2. value > 0
) as PD
WHERE IC. concept = PD. ancestor
GROUP BY PD. value
) as DCA;
The SQL query contains a subquery that calculates the value of P D(c1, c2, a) according to the values of P aths(c1, a) and P aths(c2, a) for each a ∈ CA(c1, c2). Note that the constraint a ∈ CA(a1, a2) is implemented by checking that Paths(c1, a) > 0 and Paths(c2, a) > 0. Next, another subquery groups the results of the previous query by the PD(c1, c2, a) values, and selects the most informative ancestor of each group, which represents the common disjunctive ancestors: DCA dishin (c1, c2). Finally, the query calculates the average of the information content values, i.e. the shared information: Share dishin (a1, a2)
The first subquery returns one row for each common ancestor, so the number of rows returned is limited to n. The usage of indexes on table Paths enables the computation of this subquery in constant time. Since the other subqueries only perform group and average operations over the rows returned by the first subquery, the computational complexity of the SQL query that implements DiShIn is . Note that the SQL query is universal to any ontology structured as a DAG, only the preliminary calculation of IC and Paths are dependent on the ontology used.
Semantic similarity measures have been applied to Gene Ontology (GO), a popular biomedical ontology , mainly to compare genes or proteins based on the similarity of their activities (modelled as GO concepts).
The IC was estimated using the same approach used by most measures applied to GO , where the frequency of a given concept is calculated by counting the number of proteins annotated with it or with any of its descendants in the DAG. Together with the ontology, the GO consortium also provides publicly available releases of these GO annotations.
GO also provides the transitive closure of each DAG, which was used for calculating the number of distinct paths between any pair of concepts. The calculation was performed for all pairs of concepts connected through the transitive closure. Every pair of concepts directly connected in the DAG was considered to have only one distinct path between them. And for every pair of concepts not directly connected, it was identified an intermediate concept directly connected to one of the concepts and whose number of paths to the other concept was already calculated.
A commonly used approach for evaluating semantic similarity measures in biomedical ontologies is based on comparing their correlation with structural similarity. This correlation may not be always accurate, but this approach represents a comprehensive analysis, since structural similarity is present everywhere in Molecular Biology. For example, even functional classifications, like PFAM, rely mostly on structural similarity methods . Therefore, this evaluation assumes that on average the results obtained from a large number of examples should be close to their real value, even if some exceptions exist. A systematic difference between semantic and structural similarity would undermine this assumption, but this is not expected to exist under the assumed correlation between protein function and its structure .
Recent studies on GO similarity have used CESSM, a platform that supports the collaborative and automated evaluation of similarity measures based on GO . CESSM provides an unbiased comparison of novel similarity measures against several existing ones by testing them on the same task and data, and then calculating the same performance indicators. The data are composed of a list of protein pairs, a specific release of GO and protein annotations; the task is comparing proteins; and the performance indicators are the correlation coefficients between semantic and sequence similarity.
CESSM provides a list of UniProt protein pairs which have been selected based on their quality of GO annotations, and indicates a specific release of GO and UniProt  in which the similarity should be based on. In January of 2011, CESSM was using the August of 2008 release of GO and GO-UniProt datasets and provided a list of 13,430 proteins pairs. For these proteins, we have an average of 5.9 GO annotations per protein in the Biological Process, 2.9 in the Cellular Component, and 3.7 in the Molecular Function. Thus, the DiShIn's pre-processing described above was performed over these datasets, using all protein annotations they contained (manual and electronic).
Semantic similarity measures enable a quantitative comparison between ontology concepts, but not directly between the entities annotated with them, such as proteins. To calculate protein similarity some specialized graph matching measures have been proposed, such as simGIC, but, by extension, semantic similarity measures can also be adapted to compare the entities mapped to the concepts. This adaptation has to result from combining the similarity of the concepts that the entities are mapped to. Note that an entity, such as a protein, may be mapped to multiple concepts, since proteins are usually involved in multiple biological activities. The most effective adaptation approach is composite (best-match) averages, where each concept of the first protein is paired only with the most similar concept of the second one and vice-versa [24–26]. Thus, for this study, DiShIn adopted this approach to work as a protein similarity measure.
After uploading the similarity values for each measure, CESSM provides the Pearson's linear correlation with sequence similarity , a popular approach for comparing proteins and for evaluating GO similarity measures . Therefore, this study used CESSM to obtain the correlation coefficients for the measures: Sim resnik , Sim lin , Dist jc , Simresnik:dishinand Simresnik:grasm, all adapted as protein similarity measures by using the best-match approach.
Pearson's linear correlation
Pearson's correlation coefficients
Using Fisher's transformation and a one-sample z test, Table 1 presents the p-values for the correlation coefficients of Simresnik:grasmand Simresnik:dishin, considering the null hypothesis as that these coefficients being equal to the coefficients of Sim resnik and Simresnik:grasm, respectively [, eq. 11.22]. Fisher's parametric statistics has been used by many GO applications to measure the significance of obtained results , including previous semantic similarity studies .
Confidence level on Pearson's correlation coefficients
Simresnik:dishinwas able to improve correlation because it managed to calculate the shared information in a more effective manner than Simresnik:grasmand Sim resnik . The increase is even more relevant if we take into account that multiple inheritance only affects about 10% of the GO similarity calculations. For example, we only had 5,530 out of 513,850 similarity calculations performed in the Molecular Function subontology, with Sim resnik , Simresnik:dishin. However, the best-match approach averages the GO similarity values obtained by combining the GO concepts annotated with both proteins, where a single GO similarity change may affect the final protein similarity value. Since the proteins in the CESSM dataset are all well annotated, multiple inheritance affected most of similarity values of the 13,430 protein pairs; more specifically this happened in 95% of the proteins pairs in the Biological Process, 93% in the Cellular Component, and 75% in the Molecular Function. Note that these percentages are also coherent with the edge density of each subontology, as described above. For example, in the Molecular Function subontology using only the 75% of the proteins pairs that were affected by multiple inheritance drops the correlation coefficients of Sim resnik , Simresnik:dishinand Simresnik:dishinto 0.4008, 0.4024 and 0.4149, respectively. Simresnik:dishinstill presents a significant improvement, but the lower coefficients indicate that proteins with multiple inheritance tend to have a complex biological role that is not so well correlated with sequence similarity. Nonetheless, in 10% of the cases where multiple inheritance exists, Simresnik:dishinmanaged it in a much more effective way than Simresnik:grasmin order to have achieved the overall improvement of correlation presented above. This also corroborates the hypothesis that multiple inheritance, even if scarce, can have an important overall impact, as previously proposed for GraSM. Hence, when multiple inheritance exists, it should not be neglected, as in the Resnik approach based only on the most informative common ancestor.
To exemplify how DiShIn differs from GraSM, this section discusses their values when comparing the leaf concepts of Figure 2, steroid and oxysterol 7-alpha-hydroxylase activity.
According to GraSM, these concepts have two disjunctive common ancestors: oxidoreductase with oxygen and steroid hydroxylase, whose IC in this study was 0.3846 and 0.6671, respectively. Thus, GraSM returns the average of their IC,
On the other hand, for each common ancestor, the number of paths from steroid to that ancestor is always equal to the number of paths from oxysterol to that same ancestor. For example, the top oxidoreductase has two distinct paths to each concept and steroid has one distinct path to each concept. Therefore, according to DiShIn there is only one disjunctive common ancestor, the MICA, and thus we have: Simresnik:dishin= 0.6671. Therefore, unlike GraSM, DiShIn does not penalize steroid and oxysterol for sharing parallel interpretations. Note that we cannot apply simGIC to this example, since simGIC calculates similarity between proteins (entities), not between the concepts themselves.
One of the disadvantages of using GraSM was its non-linear computational complexity. GraSM improves correlation but its execution times are about 3 times higher than using Resnik, a strong limitation due to the large size of biomedical ontologies and the vast amount of entities annotated with them.
DiShIn is not a new semantic similarity measure. In fact, it can be considered as an add-on that efficiently incorporates multiple inheritance in the calculation of the information content that two concepts share in an ontology represented as a DAG.
DiShIn was not specifically designed to measure protein similarity either. In fact, it was adapted to do so, since protein semantic and structural similarity correlation has been a generally accepted way to assess semantic similarity approaches in the biomedical field. However, semantic and structural correlation may not be the best way to assess semantic similarity, and better gold standards, not biased by structural features, are much required, especially in the case of DiShIn, where multiple inheritance is often associated with complex entities.
DiShIn does not take advantage of the higher expressivity of more advanced ontology features than the straightforward subsumption relationships present in DAGs . For semantic similarity, subsumption relationships may be enough, but as we evolve to semantic relatedness, other relationships have to be considered and additional levels of distinction between asserted and inferred hierarchies may be required.
This paper presents DiShIn, a novel method for effectively exploiting multiple inheritance when calculating the shared information content between two ontology concepts. DiShIn can be easily integrated in any semantic similarity measure dependent on the information content shared by two concepts.
DiShIn was applied to GO similarity measures, and its performance was evaluated against state-of-the-art measures using an existing platform for evaluation of protein similarity measures. In this setting, DiShIn was able to improve the correlation coefficients between semantic and sequence similarity, and also reduce the computational time of the common disjunctive ancestors identification, as previously proposed by GraSM. These results represent an important contribution towards effective management of multiple inheritance in large-scale comparative studies.
As ontologies grow and interoperability between ontologies is required , multiple inheritance will become a prominent issue for semantic similarity measures. For example, the comparison of complex biomedical entities, such as disease and epidemiological models, is a non-trivial task due to their multiple domain features and complexity. Moreover, even the single comparison of anatomical locations remains a challenge due to the lack of a common coordinate space . Thus, methods like DiShIn will certainly represent a valuable contribution for the development of multi-domain similarity measures based on an effective exploitation of multiple inheritance.
The data sets supporting the results of this article are available in the CESSM repository, http://xldb.di.fc.ul.pt/tools/cessm/.
The authors want to thank the European Commission for the financial support of the EPIWORK project under the Seventh Framework Programme (Grant #231807), and FCT (Portuguese research funding agency) for its LaSIGE Multi-annual support.
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