Evidence map›Paper›PMID 36136096›Full record

ArticleInterdisciplinary sciences, computational life sciences2023

Improving language model of human genome for DNA-protein binding prediction based on task-specific pre-training.

Hanyu Luo, Wenyu Shan, Cheng Chen, Pingjian Ding, Lingyun Luo

Abstract read
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In one paragraph

Article in Interdisciplinary sciences, computational life sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing 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.

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3 · Its place in the literature

Who cites it

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

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  8. Deciphering genomic codes using advanced natural language processing techniques: a scoping review.Journal of the American Medical Informatics Association : JAMIA · 2025
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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

5 authors.

Hanyu LuoSchool of Computer Science, University of South China, Hengyang, Hunan, 421001, People's Republic of China.
Wenyu ShanSchool of Computer Science, University of South China, Hengyang, Hunan, 421001, People's Republic of China.
Cheng ChenSchool of Computer Science, University of South China, Hengyang, Hunan, 421001, People's Republic of China.
Pingjian DingSchool of Computer Science, University of South China, Hengyang, Hunan, 421001, People's Republic of China.
Lingyun LuoSchool of Computer Science, University of South China, Hengyang, Hunan, 421001, People's Republic of China. luoly@usc.edu.cn.ORCID http://orcid.org/0000-0002-8239-9056

Funding

Innovative Research Group Project of the National Natural Science Foundation of China No. 62002154Natural Science Foundation of Hunan Province No. 2019JJ50520Natural Science Foundation of Hunan Province No. 2021JJ40467Science and Technology Innovative Research Team in Higher Educational Institutions of Hunan Province No. 20C1579Scientific Research Startup Foundation of University of South China No. 190XQD096
6 · The paper itself

Abstract

The DNA-protein binding plays a pivotal role in regulating gene expression and evolution, and computational identification of DNA-protein has drawn more and more attention in bioinformatics. Recently, variants of BERT are also used to capture the semantic information of DNA sequences for predicting DNA-protein bindings. In this study, we leverage a task-specific pre-training strategy on BERT using large-scale multi-source DNA-protein binding data and present TFBert. TFBert treats DNA sequences as natural sentences and k-mer nucleotides as words. It can effectively extract upstream and downstream nucleotide context information by pre-training the 690 unlabeled ChIP-seq datasets. Experiments show that the pre-trained model can achieve promising performance on every single dataset in the 690 ChIP-seq datasets after simple fine tuning, especially on small datasets. The average AUC is 94.7%, outperforming existing popular methods. In conclusion, this study provides a variant of BERT based on pre-training and achieved state-of-the-art results in predicting DNA-protein bindings. We believe that TFBert can provide insights into other biological sequence classification problems.

Indexed as

Genome, HumanProteinsDNAHumansLanguageProtein BindingDNAProteinsBERTBiological sequenceDNA–protein bindingPre-training

Identifiers

PMID36136096

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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.