Evidence map›Paper›PMID 35180257›Full record

ArticlePloS one2022

The application of machine learning to predict genetic relatedness using human mtDNA hypervariable region I sequences.

Priyanka Govender, Stephen Gbenga Fashoto, Leah Maharaj, Matthew A Adeleke, Elliot Mbunge, Jeremiah Olamijuwon, Boluwaji Akinnuwesi, Moses Okpeku

Abstract read
In one paragraph

Article in PloS one, 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
  2. Biological data studies, scale-up the potential with machine learning.European journal of human genetics : EJHG · 2023
    Article
  3. Overview of frequent pattern mining.Genomics & informatics · 2022
    Article
  4. 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

8 authors.

Priyanka GovenderDiscipline of Genetics, School of Life Sciences, University of KwaZulu-Natal, Westville, South Africa.
Stephen Gbenga FashotoFaculty of Science and Engineering, Department of Computer Science, Computational Intelligence and Health Informatics Research Group, University of Eswatini, Kwaluseni, Kingdom of Eswatini.
Leah MaharajDiscipline of Genetics, School of Life Sciences, University of KwaZulu-Natal, Westville, South Africa.
Matthew A AdelekeDiscipline of Genetics, School of Life Sciences, University of KwaZulu-Natal, Westville, South Africa.
Elliot MbungeFaculty of Science and Engineering, Department of Computer Science, Computational Intelligence and Health Informatics Research Group, University of Eswatini, Kwaluseni, Kingdom of Eswatini.
Jeremiah OlamijuwonFaculty of Science and Engineering, Department of Computer Science, Computational Intelligence and Health Informatics Research Group, University of Eswatini, Kwaluseni, Kingdom of Eswatini.ORCID 0000-0003-4103-2765
Boluwaji AkinnuwesiFaculty of Science and Engineering, Department of Computer Science, Computational Intelligence and Health Informatics Research Group, University of Eswatini, Kwaluseni, Kingdom of Eswatini.ORCID 0000-0002-7755-6061
Moses OkpekuDiscipline of Genetics, School of Life Sciences, University of KwaZulu-Natal, Westville, South Africa.ORCID 0000-0002-8337-6294

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human identification of unknown samples following disaster and mass casualty events is essential, especially to bring closure to family and friends of the deceased. Unfortunately, victim identification is often challenging for forensic investigators as analysis becomes complicated when biological samples are degraded or of poor quality as a result of exposure to harsh environmental factors. Mitochondrial DNA becomes the ideal option for analysis, particularly for determining the origin of the samples. In such events, the estimation of genetic parameters plays an important role in modelling and predicting genetic relatedness and is useful in assigning unknown individuals to an ethnic group. Various techniques exist for the estimation of genetic relatedness, but the use of Machine learning (ML) algorithms are novel and presently the least used in forensic genetic studies. In this study, we investigated the ability of ML algorithms to predict genetic relatedness using hypervariable region I sequences; that were retrieved from the GenBank database for three race groups, namely African, Asian and Caucasian. Four ML classification algorithms; Support vector machines (SVM), Linear discriminant analysis (LDA), Quadratic discriminant analysis (QDA) and Random Forest (RF) were hybridised with one-hot encoding, Principal component analysis (PCA) and Bags of Words (BoW), and were compared for inferring genetic relatedness. The findings from this study on WEKA showed that genetic inferences based on PCA-SVM achieved an overall accuracy of 80-90% and consistently outperformed PCA-LDA, PCA-RF and PCA-QDA, while in Python BoW-PCA-RF achieved 94.4% accuracy which outperformed BoW-PCA-SVM, BoW-PCA-LDA and BoW-PCA-QDA respectively. ML results from the use of WEKA and Python software tools displayed higher accuracies as compared to the Analysis of molecular variance results. Given the results, SVM and RF algorithms are likely to also be useful in other sequence classification applications, making it a promising tool in genetics and forensic science. The study provides evidence that ML can be utilized as a supplementary tool for forensic genetics casework analysis.

Indexed as

Machine LearningPedigreeDNA, MitochondrialForensic GeneticsHumansPolymorphism, GeneticRacial GroupsDNA, Mitochondrial

Identifiers

PMID35180257
PMCPMC8856515

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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.