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YTLR: Extracting yeast transcription factor-gene associations from the literature using automated literature readers

Cells adapt to environmental stresses mainly via transcription reprogramming. Correct transcription control is mediated by the interactions between transcription factors (TF) and their target genes. These TF-gene associations can be probed by chromatin immunoprecipitation techniques and knockout exp...

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Autores principales: Yang, Tzu-Hsien, Wang, Chung-Yu, Tsai, Hsiu-Chun, Yang, Ya-Chiao, Liu, Cheng-Tse
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449546/
https://www.ncbi.nlm.nih.gov/pubmed/36090812
http://dx.doi.org/10.1016/j.csbj.2022.08.041
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author Yang, Tzu-Hsien
Wang, Chung-Yu
Tsai, Hsiu-Chun
Yang, Ya-Chiao
Liu, Cheng-Tse
author_facet Yang, Tzu-Hsien
Wang, Chung-Yu
Tsai, Hsiu-Chun
Yang, Ya-Chiao
Liu, Cheng-Tse
author_sort Yang, Tzu-Hsien
collection PubMed
description Cells adapt to environmental stresses mainly via transcription reprogramming. Correct transcription control is mediated by the interactions between transcription factors (TF) and their target genes. These TF-gene associations can be probed by chromatin immunoprecipitation techniques and knockout experiments, revealing TF binding (TFB) and regulatory (TFR) evidence, respectively. Nevertheless, most evidence is still fragmentary in the literature and requires tremendous human resources to curate. We developed the first pipeline called YTLR (Yeast Transcription-regulation Literature Reader) to automate TF-gene relation extraction from the literature. YTLR first identifies articles with TFB and TFR information. Then TF-gene binding pairs are extracted from the TFB articles, and TF-gene regulatory associations are recognized from the TFR papers. On gathered test sets, YTLR achieves an AUC value of 98.8% in identifying articles with TFB evidence and AUC = 83.4% in extracting the detailed TF-gene binding pairs. And similarly, YTLR also obtains an AUC value of 98.2% in identifying TFR articles and AUC = 80.4% in extracting the detailed TF-gene regulatory associations. Furthermore, YTLR outperforms previous methods in both tasks. To facilitate researchers in extracting TF-gene transcriptional relations from large-scale queried articles, an automated and easy-to-use software tool based on the YTLR pipeline is constructed. In summary, YTLR aims to provide easier literature pre-screening for curators and help researchers gather yeast TF-gene transcriptional relation conclusions from articles in a high-throughput fashion. The YTLR pipeline software tool can be downloaded at https://github.com/cobisLab/YTLR/.
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spelling pubmed-94495462022-09-09 YTLR: Extracting yeast transcription factor-gene associations from the literature using automated literature readers Yang, Tzu-Hsien Wang, Chung-Yu Tsai, Hsiu-Chun Yang, Ya-Chiao Liu, Cheng-Tse Comput Struct Biotechnol J Method Article Cells adapt to environmental stresses mainly via transcription reprogramming. Correct transcription control is mediated by the interactions between transcription factors (TF) and their target genes. These TF-gene associations can be probed by chromatin immunoprecipitation techniques and knockout experiments, revealing TF binding (TFB) and regulatory (TFR) evidence, respectively. Nevertheless, most evidence is still fragmentary in the literature and requires tremendous human resources to curate. We developed the first pipeline called YTLR (Yeast Transcription-regulation Literature Reader) to automate TF-gene relation extraction from the literature. YTLR first identifies articles with TFB and TFR information. Then TF-gene binding pairs are extracted from the TFB articles, and TF-gene regulatory associations are recognized from the TFR papers. On gathered test sets, YTLR achieves an AUC value of 98.8% in identifying articles with TFB evidence and AUC = 83.4% in extracting the detailed TF-gene binding pairs. And similarly, YTLR also obtains an AUC value of 98.2% in identifying TFR articles and AUC = 80.4% in extracting the detailed TF-gene regulatory associations. Furthermore, YTLR outperforms previous methods in both tasks. To facilitate researchers in extracting TF-gene transcriptional relations from large-scale queried articles, an automated and easy-to-use software tool based on the YTLR pipeline is constructed. In summary, YTLR aims to provide easier literature pre-screening for curators and help researchers gather yeast TF-gene transcriptional relation conclusions from articles in a high-throughput fashion. The YTLR pipeline software tool can be downloaded at https://github.com/cobisLab/YTLR/. Research Network of Computational and Structural Biotechnology 2022-08-24 /pmc/articles/PMC9449546/ /pubmed/36090812 http://dx.doi.org/10.1016/j.csbj.2022.08.041 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Method Article
Yang, Tzu-Hsien
Wang, Chung-Yu
Tsai, Hsiu-Chun
Yang, Ya-Chiao
Liu, Cheng-Tse
YTLR: Extracting yeast transcription factor-gene associations from the literature using automated literature readers
title YTLR: Extracting yeast transcription factor-gene associations from the literature using automated literature readers
title_full YTLR: Extracting yeast transcription factor-gene associations from the literature using automated literature readers
title_fullStr YTLR: Extracting yeast transcription factor-gene associations from the literature using automated literature readers
title_full_unstemmed YTLR: Extracting yeast transcription factor-gene associations from the literature using automated literature readers
title_short YTLR: Extracting yeast transcription factor-gene associations from the literature using automated literature readers
title_sort ytlr: extracting yeast transcription factor-gene associations from the literature using automated literature readers
topic Method Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9449546/
https://www.ncbi.nlm.nih.gov/pubmed/36090812
http://dx.doi.org/10.1016/j.csbj.2022.08.041
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