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  1. ; ; ; ; ( , BMC Medical Informatics and Decision Making)
    Abstract Background

    Alzheimer’s Disease (AD) is a devastating disease that destroys memory and other cognitive functions. There has been an increasing research effort to prevent and treat AD. In the US, two major data sharing resources for AD research are the National Alzheimer’s Coordinating Center (NACC) and the Alzheimer’s Disease Neuroimaging Initiative (ADNI); Additionally, the National Institutes of Health (NIH) Common Data Elements (CDE) Repository has been developed to facilitate data sharing and improve the interoperability among data sets in various disease research areas.

     Method

    To better understand how AD-related data elements in these resources are interoperable with each other, we leverage different representation models to map data elements from different resources: NACC to ADNI, NACC to NIH CDE, and ADNI to NIH CDE. We explore bag-of-words based and word embeddings based models (Word2Vec and BioWordVec) to perform the data element mappings in these resources.

     Results

    The data dictionaries downloaded on November 23, 2021 contain 1,195 data elements in NACC, 13,918 in ADNI, and 27,213 in NIH CDE Repository. Data element preprocessing reduced the numbers of NACC and ADNI data elements for mapping to 1,099 and 7,584 respectively. Manual evaluation of the mapping results showed that the bag-of-words based approach achieved the best precision, while the BioWordVec based approach attained the best recall. In total, the three approaches mapped 175 out of 1,099 (15.92%) NACC data elements to ADNI; 107 out of 1,099 (9.74%) NACC data elements to NIH CDE; and 171 out of 7,584 (2.25%) ADNI data elements to NIH CDE.

     Conclusions

    The bag-of-words based and word embeddings based approaches showed promise in mapping AD-related data elements between different resources. Although the mapping approaches need further improvement, our result indicates that there is a critical need to standardize CDEs across these valuable AD research resources in order to maximize the discoveries regarding AD pathophysiology, diagnosis, and treatment that can be gleaned from them.

     
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    Free, publicly-accessible full text available April 19, 2025
  2. ; ; ( , BMC Medical Informatics and Decision Making)
    Abstract Background

    As biomedical knowledge is rapidly evolving, concept enrichment of biomedical terminologies is an active research area involving automatic identification of missing or new concepts. Previously, we prototyped a lexical-based formal concept analysis (FCA) approach in which concepts were derived by intersecting bags of words, to identify potentially missing concepts in the National Cancer Institute (NCI) Thesaurus. However, this prototype did not handle concept naming and positioning. In this paper, we introduce a sequenced-based FCA approach to identify potentially missing concepts, supporting concept naming and positioning.

     Methods

    We consider the concept name sequences as FCA attributes to construct the formal context. The concept-forming process is performed by computing the longest common substrings of concept name sequences. After new concepts are formalized, we further predict their potential positions in the original hierarchy by identifying their supertypes and subtypes from original concepts. Automated validation via external terminologies in the Unified Medical Language System (UMLS) and biomedical literature in PubMed is performed to evaluate the effectiveness of our approach.

     Results

    We applied our sequenced-based FCA approach to all the sub-hierarchies underDisease or Disorderin the NCI Thesaurus (19.08d version) and five sub-hierarchies underClinical FindingandProcedurein the SNOMED CT (US Edition, March 2020 release). In total, 1397 potentially missing concepts were identified in the NCI Thesaurus and 7223 in the SNOMED CT. For NCI Thesaurus, 85 potentially missing concepts were found in external terminologies and 315 of the remaining 1312 appeared in biomedical literature. For SNOMED CT, 576 were found in external terminologies and 1159 out of the remaining 6647 were found in biomedical literature.

     Conclusion

    Our sequence-based FCA approach has shown the promise for identifying potentially missing concepts in biomedical terminologies.

     
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  3. ; ; ( , AMIA 2021 Annual Symposium)
    Uncovering and fixing errors in biomedical terminologies is essential so that they provide accurate knowledge to downstream applications that rely on them. Non-lattice-based methods have been applied to identify various kinds of inconsistencies in different biomedical terminologies. In previous work, we have introduced two inference-based approaches that were applied in an exhaustive manner to audit hierarchical relations in the Gene Ontology: (1) Lexical-based inference framework, and (2) Subsumption-based sub-term inference framework. However, it is unclear how effective these exhaustive approaches perform compared with their corresponding non-lattice-based approaches. Therefore, in this paper, we implement the non-lattice versions of these two exhaustive approaches, and perform a comprehensive comparison between non-lattice-based and exhaustive approaches to audit the Gene Ontology. The domain expert evaluations performed for the two exhaustive approaches are leveraged to evaluate the non-lattice versions. The results indicate that the non-lattice versions have increased precision than their exhaustive counterparts even though they do not capture some of the potential inconsistencies that the exhaustive approaches identify. 
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    Accepted Manuscript Full Text Available
  4. ; ; ; ( , 2021 IEEE International Conference on Bioinformatics and Biomedicine (BIBM))
    Missing hierarchical is-a relations and missing concepts are common quality issues in biomedical ontologies. Non-lattice subgraphs have been extensively studied for automatically identifying missing is-a relations in biomedical ontologies like SNOMED CT. However, little is known about non-lattice subgraphs’ capability to uncover new or missing concepts in biomedical ontologies. In this work, we investigate a lexical-based intersection approach based on non-lattice subgraphs to identify potential missing concepts in SNOMED CT. We first construct lexical features of concepts using their fully specified names. Then we generate hierarchically unrelated concept pairs in non-lattice subgraphs as the candidates to derive new concepts. For each candidate pair of concepts, we conduct an order-preserving intersection based on the two concepts’ lexical features, with the intersection result serving as the potential new concept name suggested. We further perform automatic validation through terminologies in the Unified Medical Language System (UMLS) and literature in PubMed. Applying this approach to the March 2021 release of SNOMED CT US Edition, we obtained 7,702 potential missing concepts, among which 1,288 were validated through UMLS and 1,309 were validated through PubMed. The results showed that non-lattice subgraphs have the potential to facilitate suggestion of new concepts for SNOMED CT. 
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    Full Text Available 
  5. ; ( , 2020 IEEE International Conference on Bioinformatics and Biomedicine (BIBM))
    null (Ed.)
    Biomedical terminologies have been increasingly used in modern biomedical research and applications to facilitate data management and ensure semantic interoperability. As part of the evolution process, new concepts are regularly added to biomedical terminologies in response to the evolving domain knowledge and emerging applications. Most existing concept enrichment methods suggest new concepts via directly importing knowledge from external sources. In this paper, we introduced a lexical method based on formal concept analysis (FCA) to identify potentially missing concepts in a given terminology by leveraging its intrinsic knowledge - concept names. We first construct the FCA formal context based on the lexical features of concepts. Then we perform multistage intersection to formalize new concepts and detect potentially missing concepts. We applied our method to the Disease or Disorder sub-hierarchy in the National Cancer Institute (NCI) Thesaurus (19.08d version) and identified a total of 8,983 potentially missing concepts. As a preliminary evaluation of our method to validate the potentially missing concepts, we further checked whether they were included in any external source terminology in the Unified Medical Language System (UMLS). The result showed that 592 out of 8,937 potentially missing concepts were found in the UMLS. 
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    Full Text Available 
  6. ; ; ; ; ; ( , BMC Medical Informatics and Decision Making)
    null (Ed.)
    Abstract Background The National Cancer Institute (NCI) Thesaurus provides reference terminology for NCI and other systems. Previously, we proposed a hybrid prototype utilizing lexical features and role definitions of concepts in non-lattice subgraphs to identify missing IS-A relations in the NCI Thesaurus. However, no domain expert evaluation was provided in our previous work. In this paper, we further enhance the hybrid approach by leveraging a novel lexical feature—roots of noun chunks within concept names. Formal evaluation of our enhanced approach is also performed. Method We first compute all the non-lattice subgraphs in the NCI Thesaurus. We model each concept using its role definitions, words and roots of noun chunks within its concept name and its ancestor’s names. Then we perform subsumption testing for candidate concept pairs in the non-lattice subgraphs to automatically detect potentially missing IS-A relations. Domain experts evaluated the validity of these relations. Results We applied our approach to 19.08d version of the NCI Thesaurus. A total of 55 potentially missing IS-A relations were identified by our approach and reviewed by domain experts. 29 out of 55 were confirmed as valid by domain experts and have been incorporated in the newer versions of the NCI Thesaurus. 7 out of 55 further revealed incorrect existing IS-A relations in the NCI Thesaurus. Conclusions The results showed that our hybrid approach by leveraging lexical features and role definitions is effective in identifying potentially missing IS-A relations in the NCI Thesaurus. 
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    Full Text Available 
  7. ; ; ; ; ( , Journal of the American Medical Informatics Association)
    null (Ed.)
    Abstract Objective The Unified Medical Language System (UMLS) integrates various source terminologies to support interoperability between biomedical information systems. In this article, we introduce a novel transformation-based auditing method that leverages the UMLS knowledge to systematically identify missing hierarchical IS-A relations in the source terminologies. Materials and Methods Given a concept name in the UMLS, we first identify its base and secondary noun chunks. For each identified noun chunk, we generate replacement candidates that are more general than the noun chunk. Then, we replace the noun chunks with their replacement candidates to generate new potential concept names that may serve as supertypes of the original concept. If a newly generated name is an existing concept name in the same source terminology with the original concept, then a potentially missing IS-A relation between the original and the new concept is identified. Results Applying our transformation-based method to English-language concept names in the UMLS (2019AB release), a total of 39 359 potentially missing IS-A relations were detected in 13 source terminologies. Domain experts evaluated a random sample of 200 potentially missing IS-A relations identified in the SNOMED CT (U.S. edition) and 100 in Gene Ontology. A total of 173 of 200 and 63 of 100 potentially missing IS-A relations were confirmed by domain experts, indicating that our method achieved a precision of 86.5% and 63% for the SNOMED CT and Gene Ontology, respectively. Conclusions Our results showed that our transformation-based method is effective in identifying missing IS-A relations in the UMLS source terminologies. 
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    Full Text Available 
  8. ; ; ; ; ; ; ; ; ; ; et al ( , JCO Clinical Cancer Informatics)
    PURPOSE To audit and improve the completeness of the hierarchic (or is-a) relations of the National Cancer Institute (NCI) Thesaurus to support its role as a faceted system for querying cancer registry data. METHODS We performed quality auditing of the 19.01d version of the NCI Thesaurus. Our hybrid auditing method consisted of three main steps: computing nonlattice subgraphs, constructing lexical features for concepts in each subgraph, and performing subsumption reasoning with each subgraph to automatically suggest potentially missing is-a relations. RESULTS A total of 9,512 nonlattice subgraphs were obtained. Our method identified 925 potentially missing is-a relations in 441 nonlattice subgraphs; 72 of 176 reviewed samples were confirmed as valid missing is-a relations and have been incorporated in the newer versions of the NCI Thesaurus. CONCLUSION Autosuggested changes resulting from our auditing method can improve the structural organization of the NCI Thesaurus in supporting its new role for faceted query. 
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    Full Text Available 
  9. ; ; ; ; ; ( , Semantic Web)
    Full Text Available 
  10. ; ; ; ( , AMIA Summits on Translational Science Proceedings)
    Accepted Manuscript Full Text Available