Evidence map›Paper›PMID 38494268›Full record

ArticleJournal, genetic engineering & biotechnology2024

Human exons and introns classification using pre-trained Resnet-50 and GoogleNet models and 13-layers CNN model.

Feriel Ben Nasr Barber, Afef Elloumi Oueslati

Abstract read
In one paragraph

Article in Journal, genetic engineering & biotechnology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
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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.

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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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

2 authors.

Feriel Ben Nasr BarberElectrical Engineering Department, SITI Laboratory, National School of Engineers of Tunis (ENIT), BP37, Le Belvedere, 1002 Tunis, Tunisia; Electrical Engineering Department, National School of Engineers of Carthage (ENICarthage), Tunis, Tunisia. Electronic address: feriel.bennasr@enit.utm.tn.
Afef Elloumi OueslatiElectrical Engineering Department, SITI Laboratory, National School of Engineers of Tunis (ENIT), BP37, Le Belvedere, 1002 Tunis, Tunisia; Electrical Engineering Department, National School of Engineers of Carthage (ENICarthage), Tunis, Tunisia. Electronic address: afef.elloumi@enit.utm.tn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExamining functions and characteristics of DNA sequences is a highly challenging task. When it comes to the human genome, which is made up of exons and introns, this task is more challenging. Human exons and introns contain millions to billions of nucleotides, which contributes to the complexity observed in this sequences. Considering how complicated the subject of genomics is, it is obvious that using signal processing techniques and deep learning tools to build a strong predictive model can be very helpful for the development of the research of the human genome.

resultsAfter representing human exons and introns with color images using Frequency Chaos Game Representation, two pre-trained convolutional neural network models (Resnet-50 and GoogleNet) and a proposed CNN model having 13 hidden layers were used to classify our obtained images. We have reached a value of 92% for the accuracy rate for Resnet-50 model in about 7 h for the execution time, a value of 91.5% for the accuracy rate for the GoogleNet model in 2 h and a half for the execution time. For our proposed CNN model, we have reached 91.6% for the accuracy rate in 2 h and 37 min.

conclusionsOur proposed CNN model is faster than the Resnet-50 model in terms of execution time. It was able to slightly exceed the GoogleNet model for the accuracy rate value.

Indexed as

ClassificationCNNExonsGoogleNetIntronsRestnet-50

Identifiers

PMID38494268
PMCPMC10903757

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LicenceCC BY-NC-ND
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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.