Demo Data from EDBT 2026 / reviewers in the wild / expert
Quoc-Chinh Bui
dblp:91/8253
· DBLP profile ↗
5ranked-venue papers
4as first author
0since 2021 · last 2014
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 5 · 4 first-author
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
3 papers |
Bioinformatics and computational biology · 100% | |
| Artificial intelligence
3 papers |
Information extraction and text analysis · 100% |
Topics — the 5 heaviest of 6, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
biomedical text mining |
0.5 | 3 | 2014 | A novel feature-based approach to extract drug-drug interactions from biomedical text · Bioinform. 2014 A robust approach to extract biomedical events from literature · Bioinform. 2012 A hybrid approach to extract protein-protein interactions · Bioinform. 2011 |
Bioinformatics and computational biology › biomedical text mining
drug-drug interaction extraction |
0.2 | 1 | 2014 | A novel feature-based approach to extract drug-drug interactions from biomedical text · Bioinform. 2014 |
Bioinformatics and computational biology › biomedical text mining
biomedical event extraction |
0.1 | 1 | 2012 | A robust approach to extract biomedical events from literature · Bioinform. 2012 |
Bioinformatics and computational biology › biomedical text mining › relation extraction
protein-protein interaction extraction |
0.1 | 1 | 2011 | A hybrid approach to extract protein-protein interactions · Bioinform. 2011 |
Natural language and speech › Information extraction and text analysis › relation extraction
relation classification |
0.1 | 2 | 2014 | A novel feature-based approach to extract drug-drug interactions from biomedical text · Bioinform. 2014 A hybrid approach to extract protein-protein interactions · Bioinform. 2011 |
Methods — techniques the papers use, named apart from their topics
support vector machine · 0.6syntactic parsing · 0.4feature engineering · 0.4template-based rule learning · 0.3semantic categorization · 0.2
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2014 | A novel feature-based approach to extract drug-drug interactions from biomedical textabstractMOTIVATION: Knowledge of drug-drug interactions (DDIs) is crucial for health-care professionals to avoid adverse effects when co-administering drugs to patients. As most newly discovered DDIs are made available through scientific publications, automatic DDI extraction is highly relevant. RESULTS: We propose a novel feature-based approach to extract DDIs from text. Our approach consists of three steps. First, we apply text preprocessing to convert input sentences from a given dataset into structured representations. Second, we map each candidate DDI pair from that dataset into a suitable syntactic structure. Based on that, a novel set of features is used to generate feature vectors for these candidate DDI pairs. Third, the obtained feature vectors are used to train a support vector machine (SVM) classifier. When evaluated on two DDI extraction challenge test datasets from 2011 and 2013, our system achieves F-scores of 71.1% and 83.5%, respectively, outperforming any state-of-the-art DDI extraction system. AVAILABILITY AND IMPLEMENTATION: The source code is available for academic use at http://www.biosemantics.org/uploads/DDI.zip. Quoc-Chinh Bui, Peter M. A. Sloot, Erik M. van Mulligen, Jan A. Kors |
Bioinform. | 1 |
| 2014 | Knowledge-based extraction of adverse drug events from biomedical textabstractBACKGROUND: Many biomedical relation extraction systems are machine-learning based and have to be trained on large annotated corpora that are expensive and cumbersome to construct. We developed a knowledge-based relation extraction system that requires minimal training data, and applied the system for the extraction of adverse drug events from biomedical text. The system consists of a concept recognition module that identifies drugs and adverse effects in sentences, and a knowledge-base module that establishes whether a relation exists between the recognized concepts. The knowledge base was filled with information from the Unified Medical Language System. The performance of the system was evaluated on the ADE corpus, consisting of 1644 abstracts with manually annotated adverse drug events. Fifty abstracts were used for training, the remaining abstracts were used for testing. RESULTS: The knowledge-based system obtained an F-score of 50.5%, which was 34.4 percentage points better than the co-occurrence baseline. Increasing the training set to 400 abstracts improved the F-score to 54.3%. When the system was compared with a machine-learning system, jSRE, on a subset of the sentences in the ADE corpus, our knowledge-based system achieved an F-score that is 7 percentage points higher than the F-score of jSRE trained on 50 abstracts, and still 2 percentage points higher than jSRE trained on 90% of the corpus. CONCLUSION: A knowledge-based approach can be successfully used to extract adverse drug events from biomedical text without need for a large training set. Whether use of a knowledge base is equally advantageous for other biomedical relation-extraction tasks remains to be investigated. Ning Kang 0002, Quoc-Chinh Bui, Zubair Afzal, Erik M. van Mulligen, Jan A. Kors |
BMC Bioinform. | 3 |
| 2012 | A robust approach to extract biomedical events from literatureabstractMOTIVATION: The abundance of biomedical literature has attracted significant interest in novel methods to automatically extract biomedical relations from the literature. Until recently, most research was focused on extracting binary relations such as protein-protein interactions and drug-disease relations. However, these binary relations cannot fully represent the original biomedical data. Therefore, there is a need for methods that can extract fine-grained and complex relations known as biomedical events. RESULTS: In this article we propose a novel method to extract biomedical events from text. Our method consists of two phases. In the first phase, training data are mapped into structured representations. Based on that, templates are used to extract rules automatically. In the second phase, extraction methods are developed to process the obtained rules. When evaluated against the Genia event extraction abstract and full-text test datasets (Task 1), we obtain results with F-scores of 52.34 and 53.34, respectively, which are comparable to the state-of-the-art systems. Furthermore, our system achieves superior performance in terms of computational efficiency. AVAILABILITY: Our source code is available for academic use at http://dl.dropbox.com/u/10256952/BioEvent.zip. Quoc-Chinh Bui, Peter M. A. Sloot |
Bioinform. | 1 |
| 2011 | A hybrid approach to extract protein-protein interactionsabstractMOTIVATION: Protein-protein interactions (PPIs) play an important role in understanding biological processes. Although recent research in text mining has achieved a significant progress in automatic PPI extraction from literature, performance of existing systems still needs to be improved. RESULTS: In this study, we propose a novel algorithm for extracting PPIs from literature which consists of two phases. First, we automatically categorize the data into subsets based on its semantic properties and extract candidate PPI pairs from these subsets. Second, we apply support vector machines (SVMs) to classify candidate PPI pairs using features specific for each subset. We obtain promising results on five benchmark datasets: AIMed, BioInfer, HPRD50, IEPA and LLL with F-scores ranging from 60% to 84%, which are comparable with the state-of-the-art PPI extraction systems. Furthermore, our system achieves the best performance on cross-corpora evaluation and comparative performance in terms of computational efficiency. AVAILABILITY: The source code and scripts used in this article are available for academic use at http://staff.science.uva.nl/~bui/PPIs.zip CONTACT: [email protected]. Quoc-Chinh Bui, Sophia Katrenko, Peter M. A. Sloot |
Bioinform. | 1 |
| 2010 | Extracting causal relations on HIV drug resistance from literatureabstractBACKGROUND: In HIV treatment it is critical to have up-to-date resistance data of applicable drugs since HIV has a very high rate of mutation. These data are made available through scientific publications and must be extracted manually by experts in order to be used by virologists and medical doctors. Therefore there is an urgent need for a tool that partially automates this process and is able to retrieve relations between drugs and virus mutations from literature. RESULTS: In this work we present a novel method to extract and combine relationships between HIV drugs and mutations in viral genomes. Our extraction method is based on natural language processing (NLP) which produces grammatical relations and applies a set of rules to these relations. We applied our method to a relevant set of PubMed abstracts and obtained 2,434 extracted relations with an estimated performance of 84% for F-score. We then combined the extracted relations using logistic regression to generate resistance values for each pair. The results of this relation combination show more than 85% agreement with the Stanford HIVDB for the ten most frequently occurring mutations. The system is used in 5 hospitals from the Virolab project http://www.virolab.org to preselect the most relevant novel resistance data from literature and present those to virologists and medical doctors for further evaluation. CONCLUSIONS: The proposed relation extraction and combination method has a good performance on extracting HIV drug resistance data. It can be used in large-scale relation extraction experiments. The developed methods can also be applied to extract other type of relations such as gene-protein, gene-disease, and disease-mutation. Quoc-Chinh Bui, Breanndán Ó Nualláin, Charles A. Boucher, Peter M. A. Sloot |
BMC Bioinform. | 1 |