Evidence map›Paper›PMID 38572749›Full record

ArticleNucleic acids research2024

Discovering DNA shape motifs with multiple DNA shape features: generalization, methods, and validation.

Nanjun Chen, Jixiang Yu, Zhe Liu, Lingkuan Meng, Xiangtao Li, Ka-Chun Wong

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.1field-weighted citation impact, top 13% of its field
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

5 citing papers in PubMed, 9 citations in OpenAlex.

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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

6 authors at 2 institutions in 2 countries.

Nanjun ChenDepartment of Computer Science, City University of Hong Kong, Kowloon Tong, Hong Kong SAR.ORCID 0000-0003-1432-3495
Jixiang YuDepartment of Computer Science, City University of Hong Kong, Kowloon Tong, Hong Kong SAR.ORCID 0000-0001-8163-3253
Zhe LiuDepartment of Computer Science, City University of Hong Kong, Kowloon Tong, Hong Kong SAR.ORCID 0000-0003-0726-2727
Lingkuan MengDepartment of Computer Science, City University of Hong Kong, Kowloon Tong, Hong Kong SAR.ORCID 0000-0003-0909-6849
Xiangtao LiSchool of Artificial Intelligence, Jilin University, Changchun City, Jilin Province, China.ORCID 0000-0002-8716-9823
Ka-Chun WongDepartment of Computer Science, City University of Hong Kong, Kowloon Tong, Hong Kong SAR.ORCID 0000-0001-6062-733X
City University of Hong Kong · HKJilin University · CN

Funding

City University of Hong Kong 2021SIRG036Innovation and Technology Commission ITB/FBL/9037/22/SNational Natural Science Foundation of China 32170654Research Grants Council of the Hong Kong Special Administrative Region CityU 11203723
6 · The paper itself

Abstract

DNA motifs are crucial patterns in gene regulation. DNA-binding proteins (DBPs), including transcription factors, can bind to specific DNA motifs to regulate gene expression and other cellular activities. Past studies suggest that DNA shape features could be subtly involved in DNA-DBP interactions. Therefore, the shape motif annotations based on intrinsic DNA topology can deepen the understanding of DNA-DBP binding. Nevertheless, high-throughput tools for DNA shape motif discovery that incorporate multiple features altogether remain insufficient. To address it, we propose a series of methods to discover non-redundant DNA shape motifs with the generalization to multiple motifs in multiple shape features. Specifically, an existing Gibbs sampling method is generalized to multiple DNA motif discovery with multiple shape features. Meanwhile, an expectation-maximization (EM) method and a hybrid method coupling EM with Gibbs sampling are proposed and developed with promising performance, convergence capability, and efficiency. The discovered DNA shape motif instances reveal insights into low-signal ChIP-seq peak summits, complementing the existing sequence motif discovery works. Additionally, our modelling captures the potential interplays across multiple DNA shape features. We provide a valuable platform of tools for DNA shape motif discovery. An R package is built for open accessibility and long-lasting impact: https://zenodo.org/doi/10.5281/zenodo.10558980.

Indexed as

DNANucleotide MotifsAlgorithmsBinding SitesChromatin Immunoprecipitation SequencingDNA-Binding ProteinsHumansNucleic Acid ConformationProtein BindingTranscription FactorsDNADNA-Binding ProteinsTranscription Factors

Identifiers

PMID38572749
PMCPMC11077088
OpenAlexW4393947775

What OpenQuestion holds

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LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.