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The effect of mislabeled phenotypic status on the identification of mutation-carriers from SNP genotypes in dairy cattle
BACKGROUND: Statistical and machine learning applications are increasingly popular in animal breeding and genetics, especially to compute genomic predictions for phenotypes of interest. Noise (errors) in the data may have a negative impact on the accuracy of predictions. The effects of noisy data ha...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485573/ https://www.ncbi.nlm.nih.gov/pubmed/28651561 http://dx.doi.org/10.1186/s13104-017-2540-x |
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author | Biffani, Stefano Pausch, Hubert Schwarzenbacher, Hermann Biscarini, Filippo |
author_facet | Biffani, Stefano Pausch, Hubert Schwarzenbacher, Hermann Biscarini, Filippo |
author_sort | Biffani, Stefano |
collection | PubMed |
description | BACKGROUND: Statistical and machine learning applications are increasingly popular in animal breeding and genetics, especially to compute genomic predictions for phenotypes of interest. Noise (errors) in the data may have a negative impact on the accuracy of predictions. The effects of noisy data have been investigated in genome-wide association studies for case–control experiments, and in genomic predictions for binary traits in plants. No studies have been published yet on the impact of noisy data in animal genomics. In this work, the susceptibility to noise of five classification models (Lasso-penalised logistic regression—Lasso, K-nearest neighbours—KNN, random forest—RF, support vector machines with linear—SVML—or radial—SVMR—kernel) was tested. As illustration, the identification of carriers of a recessive mutation in cattle (Bos taurus) was used. A population of 3116 Fleckvieh animals with SNP genotypes on the same chromosome as the mutation locus (BTA 19) was available. The carrier status (0/1 phenotype) was randomly sampled to generate noise. Increasing proportions of noise—up to 20%— were introduced in the data. RESULTS: SVMR and Lasso were relatively more robust to noise in the data, with total accuracy still above 0.975 and TPR (true positive rate; accuracy in the minority class) in the range 0.5–0.80 also with 17.5–20% mislabeled observations. The performance of SVML and RF decreased monotonically with increasing noise in the data, while KNN constantly failed to identify mutation carriers (observations in the minority class). The computation time increased with noise in the data, especially for the two support vector machines classifiers. CONCLUSIONS: This work was the first to assess the impact of phenotyping errors on the accuracy of genomic predictions in animal genetics. The choice of the classification method can influence results in terms of higher or lower susceptibility to noise. In the presented problem, SVM with radial kernel performed relatively well even when the proportion of errors in the data reached 12.5%. Lasso was the second best method, while SVML, RF and KNN were very sensitive to noise. Taking into account both accuracy and computation time, Lasso provided the best combination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-017-2540-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5485573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54855732017-06-30 The effect of mislabeled phenotypic status on the identification of mutation-carriers from SNP genotypes in dairy cattle Biffani, Stefano Pausch, Hubert Schwarzenbacher, Hermann Biscarini, Filippo BMC Res Notes Research Article BACKGROUND: Statistical and machine learning applications are increasingly popular in animal breeding and genetics, especially to compute genomic predictions for phenotypes of interest. Noise (errors) in the data may have a negative impact on the accuracy of predictions. The effects of noisy data have been investigated in genome-wide association studies for case–control experiments, and in genomic predictions for binary traits in plants. No studies have been published yet on the impact of noisy data in animal genomics. In this work, the susceptibility to noise of five classification models (Lasso-penalised logistic regression—Lasso, K-nearest neighbours—KNN, random forest—RF, support vector machines with linear—SVML—or radial—SVMR—kernel) was tested. As illustration, the identification of carriers of a recessive mutation in cattle (Bos taurus) was used. A population of 3116 Fleckvieh animals with SNP genotypes on the same chromosome as the mutation locus (BTA 19) was available. The carrier status (0/1 phenotype) was randomly sampled to generate noise. Increasing proportions of noise—up to 20%— were introduced in the data. RESULTS: SVMR and Lasso were relatively more robust to noise in the data, with total accuracy still above 0.975 and TPR (true positive rate; accuracy in the minority class) in the range 0.5–0.80 also with 17.5–20% mislabeled observations. The performance of SVML and RF decreased monotonically with increasing noise in the data, while KNN constantly failed to identify mutation carriers (observations in the minority class). The computation time increased with noise in the data, especially for the two support vector machines classifiers. CONCLUSIONS: This work was the first to assess the impact of phenotyping errors on the accuracy of genomic predictions in animal genetics. The choice of the classification method can influence results in terms of higher or lower susceptibility to noise. In the presented problem, SVM with radial kernel performed relatively well even when the proportion of errors in the data reached 12.5%. Lasso was the second best method, while SVML, RF and KNN were very sensitive to noise. Taking into account both accuracy and computation time, Lasso provided the best combination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13104-017-2540-x) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-26 /pmc/articles/PMC5485573/ /pubmed/28651561 http://dx.doi.org/10.1186/s13104-017-2540-x Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Biffani, Stefano Pausch, Hubert Schwarzenbacher, Hermann Biscarini, Filippo The effect of mislabeled phenotypic status on the identification of mutation-carriers from SNP genotypes in dairy cattle |
title | The effect of mislabeled phenotypic status on the identification of mutation-carriers from SNP genotypes in dairy cattle |
title_full | The effect of mislabeled phenotypic status on the identification of mutation-carriers from SNP genotypes in dairy cattle |
title_fullStr | The effect of mislabeled phenotypic status on the identification of mutation-carriers from SNP genotypes in dairy cattle |
title_full_unstemmed | The effect of mislabeled phenotypic status on the identification of mutation-carriers from SNP genotypes in dairy cattle |
title_short | The effect of mislabeled phenotypic status on the identification of mutation-carriers from SNP genotypes in dairy cattle |
title_sort | effect of mislabeled phenotypic status on the identification of mutation-carriers from snp genotypes in dairy cattle |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5485573/ https://www.ncbi.nlm.nih.gov/pubmed/28651561 http://dx.doi.org/10.1186/s13104-017-2540-x |
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