Evidence map›Paper›PMID 36671456›Full record

ArticleBiomolecules2022

An Efficient Lightweight Hybrid Model with Attention Mechanism for Enhancer Sequence Recognition.

Suliman Aladhadh, Saleh A Almatroodi, Shabana Habib, Abdulatif Alabdulatif, Saeed Ullah Khattak, Muhammad Islam

Abstract read
In one paragraph

Article in Biomolecules, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
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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.

Suliman AladhadhDepartment of Information Technology, College of Computer, Qassim University, Buraydah 51452, Saudi Arabia.ORCID 0000-0003-4349-8710
Saleh A AlmatroodiDepartment of Medical Laboratories, College of Applied Medical Sciences, Qassim University, Buraydah 51452, Saudi Arabia.ORCID 0000-0002-5260-0265
Shabana HabibDepartment of Information Technology, College of Computer, Qassim University, Buraydah 51452, Saudi Arabia.ORCID 0000-0002-6543-2520
Abdulatif AlabdulatifDepartment of Computer Science, College of Computer, Qassim University, Buraydah 51452, Saudi Arabia.ORCID 0000-0003-0646-5872
Saeed Ullah KhattakCentre of Biotechnology and Microbiology, University of Peshawar, Peshawar 25120, Pakistan.
Muhammad IslamDepartment of Electrical Engineering, College of Engineering and Information Technology, Onaizah Colleges, Onaizah 56447, Saudi Arabia.ORCID 0000-0002-2379-4451

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Enhancers are sequences with short motifs that exhibit high positional variability and free scattering properties. Identification of these noncoding DNA fragments and their strength are extremely important because they play a key role in controlling gene regulation on a cellular basis. The identification of enhancers is more complex than that of other factors in the genome because they are freely scattered, and their location varies widely. In recent years, bioinformatics tools have enabled significant improvement in identifying this biological difficulty. Cell line-specific screening is not possible using these existing computational methods based solely on DNA sequences. DNA segment chromatin accessibility may provide useful information about its potential function in regulation, thereby identifying regulatory elements based on its chromatin accessibility. In chromatin, the entanglement structure allows positions far apart in the sequence to encounter each other, regardless of their proximity to the gene to be acted upon. Thus, identifying enhancers and assessing their strength is difficult and time-consuming. The goal of our work was to overcome these limitations by presenting a convolutional neural network (CNN) with attention-gated recurrent units (AttGRU) based on Deep Learning. It used a CNN and one-hot coding to build models, primarily to identify enhancers and secondarily to classify their strength. To test the performance of the proposed model, parallels were drawn between enhancer-CNNAttGRU and existing state-of-the-art methods to enable comparisons. The proposed model performed the best for predicting stage one and stage two enhancer sequences, as well as their strengths, in a cross-species analysis, achieving best accuracy values of 87.39% and 84.46%, respectively. Overall, the results showed that the proposed model provided comparable results to state-of-the-art models, highlighting its usefulness.

Indexed as

ChromatinEnhancer Elements, GeneticComputational BiologyDNANeural Networks, ComputerChromatinDNAconvolution neural networkdeep learningenhancer sequencesequential learning modelstemporal attention mechanism

Identifiers

PMID36671456
PMCPMC9855522

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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.