ArticleBMC bioinformatics2015
Semi-supervised Learning for the BioNLP Gene Regulation Network.
Article in BMC bioinformatics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- Multimodal Collaborative Modeling of Molecular Structures and Biomedical Text for Accurate Drug-Drug Interaction Extraction.Biomedicines · 2026Article
- Artificial Intelligence and Cardiovascular Genetics.Life (Basel, Switzerland) · 2022Review
- Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThe BioNLP Gene Regulation Task has attracted a diverse collection of submissions showcasing state-of-the-art systems. However, a principal challenge remains in obtaining a significant amount of recall. We argue that this is an important quality for Information Extraction tasks in this field. We propose a semi-supervised framework, leveraging a large corpus of unannotated data available to us. In this framework, the annotated data is used to find plausible candidates for positive data points, which are included in the machine learning process. As this is a method principally designed for gaining recall, we further explore additional methods to improve precision on top of this. These are: weighted regularisation in the SVM framework, and filtering out unlabelled examples based on a probabilistic rule-finding method. The latter method also allows us to add candidates for negatives from unlabelled data, a method not viable in the unfiltered approach.
resultsWe replicate one of the original participant systems, and modify it to incorporate our methods. This allows us to test the extent of our proposed methods by applying them to the GRN task data. We find a considerable improvement in recall compared to the baseline system. We also investigate the evaluation metrics and find several mechanisms explaining a bias towards precision. Furthermore, these findings uncover an intricate precision-recall interaction, depriving recall of its habitual immediacy seen in traditional machine learning set-ups.
conclusionOur contributions are twofold.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.