Evidence map›Paper›PMID 38764593›Full record

ArticleArXiv2023

Evaluation of GPT and BERT-based models on identifying proteinprotein interactions in biomedical text.

Hasin Rehana, Nur Bengisu Çam, Mert Basmaci, Jie Zheng, Christianah Jemiyo, Yongqun He, Arzucan Özgür, Junguk Hur

Abstract readPreprint
In one paragraph

Article in ArXiv, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Hasin RehanaComputer Science Graduate Program, University of North Dakota, Grand Forks, North Dakota, 58202, USA.
Nur Bengisu ÇamDepartment of Computer Engineering, Bogazici University, 34342 Istanbul, Turkey.
Mert BasmaciDepartment of Computer Engineering, Bogazici University, 34342 Istanbul, Turkey.
Jie ZhengUnit for Laboratory Animal Medicine, Department of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, 48109, USA.
Christianah JemiyoDepartment of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota, 58202, USA.
Yongqun HeUnit for Laboratory Animal Medicine, Department of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan, 48109, USA.
Arzucan ÖzgürDepartment of Computer Engineering, Bogazici University, 34342 Istanbul, Turkey.
Junguk HurDepartment of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, North Dakota, 58202, USA.

Funding

VIOLIN 2.0: Vaccine Information and Ontology LInked kNowledgebaseU24AI171008 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Yongqun He, Junguk Hur · 2022 to 2026
$4.2M
NIAID NIH HHS U24 AI171008
6 · The paper itself

Abstract

Detecting protein-protein interactions (PPIs) is crucial for understanding genetic mechanisms, disease pathogenesis, and drug design. However, with the fast-paced growth of biomedical literature, there is a growing need for automated and accurate extraction of PPIs to facilitate scientific knowledge discovery. Pre-trained language models, such as generative pre-trained transformers (GPT) and bidirectional encoder representations from transformers (BERT), have shown promising results in natural language processing (NLP) tasks. We evaluated the performance of PPI identification of multiple GPT and BERT models using three manually curated gold-standard corpora: Learning Language in Logic (LLL) with 164 PPIs in 77 sentences, Human Protein Reference Database with 163 PPIs in 145 sentences, and Interaction Extraction Performance Assessment with 335 PPIs in 486 sentences. BERT-based models achieved the best overall performance, with BioBERT achieving the highest recall (91.95%) and F1-score (86.84%) and PubMedBERT achieving the highest precision (85.25%). Interestingly, despite not being explicitly trained for biomedical texts, GPT-4 achieved commendable performance, comparable to the top-performing BERT models. It achieved a precision of 88.37%, a recall of 85.14%, and an F1-score of 86.49% on the LLL dataset. These results suggest that GPT models can effectively detect PPIs from text data, offering promising avenues for application in biomedical literature mining. Further research could explore how these models might be fine-tuned for even more specialized tasks within the biomedical domain.

Identifiers

PMID38764593
PMCPMC11101131

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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.