Evidence map›Paper›PMID 39213391›Full record

ArticleDatabase : the journal of biological databases and curation2024

Automatic extraction of transcriptional regulatory interactions of bacteria from biomedical literature using a BERT-based approach.

Alfredo Varela-Vega, Ali-Berenice Posada-Reyes, Carlos-Francisco Méndez-Cruz

Abstract read
In one paragraph

Article in Database : the journal of biological databases and curation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

3 authors.

Alfredo Varela-VegaPrograma de Genómica Computacional, Centro de Ciencias Genómicas, UNAM, Av. Universidad S/N Col. Chamilpa, Cuernavaca, Morelos 62210, México.ORCID 0000-0003-4857-4997
Ali-Berenice Posada-ReyesLaboratorio de Microbiología, Inmunología y Salud Pública, Facultad de Estudios Superiores Cuautitlán, UNAM, Carretera Cuautitlán-Teoloyucan Km. 2.5, Xhala, Cuautitlán Izcalli, Estado de México 54714, México.ORCID 0000-0003-3165-6099
Carlos-Francisco Méndez-CruzPrograma de Genómica Computacional, Centro de Ciencias Genómicas, UNAM, Av. Universidad S/N Col. Chamilpa, Cuernavaca, Morelos 62210, México.ORCID 0000-0002-2549-1614

Funding

Dirección General de Asuntos del Personal Académico, Universidad Nacional Autónoma de México IN219523
6 · The paper itself

Abstract

Transcriptional regulatory networks (TRNs) give a global view of the regulatory mechanisms of bacteria to respond to environmental signals. These networks are published in biological databases as a valuable resource for experimental and bioinformatics researchers. Despite the efforts to publish TRNs of diverse bacteria, many of them still lack one and many of the existing TRNs are incomplete. In addition, the manual extraction of information from biomedical literature ("literature curation") has been the traditional way to extract these networks, despite this being demanding and time-consuming. Recently, language models based on pretrained transformers have been used to extract relevant knowledge from biomedical literature. Moreover, the benefit of fine-tuning a large pretrained model with new limited data for a specific task ("transfer learning") opens roads to address new problems of biomedical information extraction. Here, to alleviate this lack of knowledge and assist literature curation, we present a new approach based on the Bidirectional Transformer for Language Understanding (BERT) architecture to classify transcriptional regulatory interactions of bacteria as a first step to extract TRNs from literature. The approach achieved a significant performance in a test dataset of sentences of Escherichia coli (F1-Score: 0.8685, Matthew's correlation coefficient: 0.8163). The examination of model predictions revealed that the model learned different ways to express the regulatory interaction. The approach was evaluated to extract a TRN of Salmonella using 264 complete articles. The evaluation showed that the approach was able to accurately extract 82% of the network and that it was able to extract interactions absent in curation data. To the best of our knowledge, the present study is the first effort to obtain a BERT-based approach to extract this specific kind of interaction. This approach is a starting point to address the limitations of reconstructing TRNs of bacteria and diseases of biological interest. Database URL: https://github.com/laigen-unam/BERT-trn-extraction.

Indexed as

Gene Regulatory NetworksBacteriaComputational BiologyDatabases, GeneticData CurationData Mining

Identifiers

PMID39213391
PMCPMC11363960

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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.