Evidence map›Paper›PMID 35263332›Full record

ArticlePLoS computational biology2022

Base-resolution prediction of transcription factor binding signals by a deep learning framework.

Qinhu Zhang, Ying He, Siguo Wang, Zhanheng Chen, Zhenhao Guo, Zhen Cui, Qi Liu, De-Shuang Huang

Abstract read
In one paragraph

Article in PLoS computational biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–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

13 citing papers in PubMed.

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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

8 authors.

Qinhu ZhangTranslational Medical Center for Stem Cell Therapy and Institute for Regenerative Medicine, Shanghai East Hospital, Bioinformatics Department, School of Life Sciences and Technology, Tongji University, Shanghai, China.ORCID 0000-0002-4232-7736
Ying HeInstitute of Machine Learning and Systems Biology, School of Electronics and Information Engineering, Tongji University, Shanghai, China.ORCID 0000-0002-9592-7727
Siguo WangInstitute of Machine Learning and Systems Biology, School of Electronics and Information Engineering, Tongji University, Shanghai, China.ORCID 0000-0002-3244-3629
Zhanheng ChenCollege of Computer Science and Software Engineering, Shenzhen University, Shenzhen, China.
Zhenhao GuoInstitute of Machine Learning and Systems Biology, School of Electronics and Information Engineering, Tongji University, Shanghai, China.
Zhen CuiInstitute of Machine Learning and Systems Biology, School of Electronics and Information Engineering, Tongji University, Shanghai, China.ORCID 0000-0001-5522-6750
Qi LiuTranslational Medical Center for Stem Cell Therapy and Institute for Regenerative Medicine, Shanghai East Hospital, Bioinformatics Department, School of Life Sciences and Technology, Tongji University, Shanghai, China.
De-Shuang HuangInstitute of Machine Learning and Systems Biology, School of Electronics and Information Engineering, Tongji University, Shanghai, China.ORCID 0000-0002-6759-2691

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcription factors (TFs) play an important role in regulating gene expression, thus the identification of the sites bound by them has become a fundamental step for molecular and cellular biology. In this paper, we developed a deep learning framework leveraging existing fully convolutional neural networks (FCN) to predict TF-DNA binding signals at the base-resolution level (named as FCNsignal). The proposed FCNsignal can simultaneously achieve the following tasks: (i) modeling the base-resolution signals of binding regions; (ii) discriminating binding or non-binding regions; (iii) locating TF-DNA binding regions; (iv) predicting binding motifs. Besides, FCNsignal can also be used to predict opening regions across the whole genome. The experimental results on 53 TF ChIP-seq datasets and 6 chromatin accessibility ATAC-seq datasets show that our proposed framework outperforms some existing state-of-the-art methods. In addition, we explored to use the trained FCNsignal to locate all potential TF-DNA binding regions on a whole chromosome and predict DNA sequences of arbitrary length, and the results show that our framework can find most of the known binding regions and accept sequences of arbitrary length. Furthermore, we demonstrated the potential ability of our framework in discovering causal disease-associated single-nucleotide polymorphisms (SNPs) through a series of experiments.

Indexed as

Deep LearningBinding SitesChromatin Immunoprecipitation SequencingProtein BindingTranscription FactorsTranscription Factors

Identifiers

PMID35263332
PMCPMC8982852

What OpenQuestion holds

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Registered trials

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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.