Evidence map›Paper›PMID 33101452›Full record

ArticleBiomedical signal processing and control2021

New methodology for repetitive sequences identification in

Rabeb Touati, Asma Tajouri, Imen Mesaoudi, Afef Elloumi Oueslati, Zied Lachiri, Maher Kharrat

Open access · greenAbstract read
In one paragraph

Article in Biomedical signal processing and control, 2021. 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
0.4field-weighted citation impact, top 39% 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

4 citing papers in PubMed, 8 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 1 country.

Rabeb TouatiUniversity of Tunis El Manar, LR99ES10 Human Genetics Laboratory, Faculty of Medicine of Tunis (FMT), Tunisia.
Asma TajouriUniversity of Tunis El Manar, LR99ES10 Human Genetics Laboratory, Faculty of Medicine of Tunis (FMT), Tunisia.
Imen MesaoudiUniversity of Tunis El Manar, SITI Laboratory, National School of Engineers of Tunis, BP 37, Le Belvédère, 1002, Tunis, Tunisia.
Afef Elloumi OueslatiUniversity of Tunis El Manar, SITI Laboratory, National School of Engineers of Tunis, BP 37, Le Belvédère, 1002, Tunis, Tunisia.
Zied LachiriUniversity of Tunis El Manar, SITI Laboratory, National School of Engineers of Tunis, BP 37, Le Belvédère, 1002, Tunis, Tunisia.
Maher KharratUniversity of Tunis El Manar, LR99ES10 Human Genetics Laboratory, Faculty of Medicine of Tunis (FMT), Tunisia.
National Engineering School of Tunis · TNFaculté de médecine de Tunis

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Repetitive DNA sequences occupy the major proportion of DNA in the human genome and even in the other species' genomes. The importance of each repetitive DNA type depends on many factors: structural and functional roles, positions, lengths and numbers of these repetitions are clear examples. Conserving such DNA sequences or not in different locations in the chromosome remains a challenge for researchers in biology. Detecting their location despite their great variability and finding novel repetitive sequences remains a challenging task. To side-step this problem, we developed a new method based on signal and image processing tools. In fact, using this method we could find repetitive patterns in DNA images regardless of the repetition length. This new technique seems to be more efficient in detecting new repetitive sequences than bioinformatics tools. In fact, the classical tools present limited performances especially in case of mutations (insertion or deletion). However, modifying one or a few numbers of pixels in the image doesn't affect the global form of the repetitive pattern. As a consequence, we generated a new repetitive patterns database which contains tandem and dispersed repeated sequences. The highly repetitive sequences, we have identified in X and Y chromosomes, are shown to be located in other human chromosomes or in other genomes. The data we have generated is then taken as input to a Convolutional neural network classifier in order to classify them. The system we have constructed is efficient and gives an average of 94.4% as recognition score.

Indexed as

Canny edge detectionConvolutional neural network (CNN)Human genomeNew repetitions databaseRepetitive sequencesSatellitesWavelet transform

Identifiers

PMID33101452
PMCPMC7572123
OpenAlexW3093941455

What OpenQuestion holds

Textmetadata
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.