Evidence map›Paper›PMID 34183066›Full record

ArticleBioData mining2021

New neural network classification method for individuals ancestry prediction from SNPs data.

H Soumare, S Rezgui, N Gmati, A Benkahla

Open access · goldAbstract read
In one paragraph

Article in BioData mining, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
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

4 authors at 3 institutions in 2 countries.

H SoumareThe Laboratory of Mathematical Modelling and Numeric in Engineering Sciences, National Engineering School of Tunis, Rue Béchir Salem Belkhiria Campus universitaire, B.P. 37, 1002 Tunis Belvédère, University of Tunis El Manar, Tunis, Tunisia. soumare.harouna@enit.utm.tn.ORCID http://orcid.org/0000-0002-5326-7783
S RezguiADAGOS. Le Belvédère centre, 61 rue El Khartoum, El Menzah, Tunis, Tunisia.
N GmatiCollege of sciences & Basic and Applied Scientific Research Center, Imam Abdulrahman Bin Faisal University, P.O. Box 1982, 31441, Dammam, Kingdom of Saudi Arabia, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
A BenkahlaLaboratory of BioInformatics, bioMathematics, and bioStatistics, 13 place Pasteur, B.P. 74 1002 Tunis, Belvédère, Institut Pasteur de Tunis, University of Tunis El Manar, Tunis, Tunisia.
Imam Abdulrahman Bin Faisal University · SANational Engineering School of Tunis · TNTunis University · TN

Funding

H3ABioNet: a sustainable African Bioinformatics Network for H3AfricaU41HG006941 · NHGRI · UNIVERSITY OF CAPE TOWN · PI MULDER, NICOLA · 2012 to 2017
$14.8M
NHGRI NIH HHS U41 HG006941
6 · The paper itself

Abstract

Artificial Neural Network (ANN) algorithms have been widely used to analyse genomic data. Single Nucleotide Polymorphisms(SNPs) represent the genetic variations, the most common in the human genome, it has been shown that they are involved in many genetic diseases, and can be used to predict their development. Developing ANN to handle this type of data can be considered as a great success in the medical world. However, the high dimensionality of genomic data and the availability of a limited number of samples can make the learning task very complicated. In this work, we propose a New Neural Network classification method based on input perturbation. The idea is first to use SVD to reduce the dimensionality of the input data and to train a classification network, which prediction errors are then reduced by perturbing the SVD projection matrix. The proposed method has been evaluated on data from individuals with different ancestral origins, the experimental results have shown the effectiveness of the proposed method. Achieving up to 96.23% of classification accuracy, this approach surpasses previous Deep learning approaches evaluated on the same dataset.

Indexed as

Artificial neural networkDimensionality reductionInput perturbationSingle nucleotide polymorphismSingular value decomposition

Identifiers

PMID34183066
PMCPMC8240223
OpenAlexW3111384249

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.