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Feature weighted models to address lineage dependency in drug-resistance prediction from Mycobacterium tuberculosis genome sequences
MOTIVATION: Tuberculosis (TB) is caused by members of the Mycobacterium tuberculosis complex (MTBC), which has a strain- or lineage-based clonal population structure. The evolution of drug-resistance in the MTBC poses a threat to successful treatment and eradication of TB. Machine learning approache...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351970/ https://www.ncbi.nlm.nih.gov/pubmed/37428143 http://dx.doi.org/10.1093/bioinformatics/btad428 |
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author | Billows, Nina Phelan, Jody E Xia, Dong Peng, Yonghong Clark, Taane G Chang, Yu-Mei |
author_facet | Billows, Nina Phelan, Jody E Xia, Dong Peng, Yonghong Clark, Taane G Chang, Yu-Mei |
author_sort | Billows, Nina |
collection | PubMed |
description | MOTIVATION: Tuberculosis (TB) is caused by members of the Mycobacterium tuberculosis complex (MTBC), which has a strain- or lineage-based clonal population structure. The evolution of drug-resistance in the MTBC poses a threat to successful treatment and eradication of TB. Machine learning approaches are being increasingly adopted to predict drug-resistance and characterize underlying mutations from whole genome sequences. However, such approaches may not generalize well in clinical practice due to confounding from the population structure of the MTBC. RESULTS: To investigate how population structure affects machine learning prediction, we compared three different approaches to reduce lineage dependency in random forest (RF) models, including stratification, feature selection, and feature weighted models. All RF models achieved moderate-high performance (area under the ROC curve range: 0.60–0.98). First-line drugs had higher performance than second-line drugs, but it varied depending on the lineages in the training dataset. Lineage-specific models generally had higher sensitivity than global models which may be underpinned by strain-specific drug-resistance mutations or sampling effects. The application of feature weights and feature selection approaches reduced lineage dependency in the model and had comparable performance to unweighted RF models. AVAILABILITY AND IMPLEMENTATION: https://github.com/NinaMercedes/RF_lineages. |
format | Online Article Text |
id | pubmed-10351970 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-103519702023-07-18 Feature weighted models to address lineage dependency in drug-resistance prediction from Mycobacterium tuberculosis genome sequences Billows, Nina Phelan, Jody E Xia, Dong Peng, Yonghong Clark, Taane G Chang, Yu-Mei Bioinformatics Original Paper MOTIVATION: Tuberculosis (TB) is caused by members of the Mycobacterium tuberculosis complex (MTBC), which has a strain- or lineage-based clonal population structure. The evolution of drug-resistance in the MTBC poses a threat to successful treatment and eradication of TB. Machine learning approaches are being increasingly adopted to predict drug-resistance and characterize underlying mutations from whole genome sequences. However, such approaches may not generalize well in clinical practice due to confounding from the population structure of the MTBC. RESULTS: To investigate how population structure affects machine learning prediction, we compared three different approaches to reduce lineage dependency in random forest (RF) models, including stratification, feature selection, and feature weighted models. All RF models achieved moderate-high performance (area under the ROC curve range: 0.60–0.98). First-line drugs had higher performance than second-line drugs, but it varied depending on the lineages in the training dataset. Lineage-specific models generally had higher sensitivity than global models which may be underpinned by strain-specific drug-resistance mutations or sampling effects. The application of feature weights and feature selection approaches reduced lineage dependency in the model and had comparable performance to unweighted RF models. AVAILABILITY AND IMPLEMENTATION: https://github.com/NinaMercedes/RF_lineages. Oxford University Press 2023-07-10 /pmc/articles/PMC10351970/ /pubmed/37428143 http://dx.doi.org/10.1093/bioinformatics/btad428 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Billows, Nina Phelan, Jody E Xia, Dong Peng, Yonghong Clark, Taane G Chang, Yu-Mei Feature weighted models to address lineage dependency in drug-resistance prediction from Mycobacterium tuberculosis genome sequences |
title | Feature weighted models to address lineage dependency in drug-resistance prediction from Mycobacterium tuberculosis genome sequences |
title_full | Feature weighted models to address lineage dependency in drug-resistance prediction from Mycobacterium tuberculosis genome sequences |
title_fullStr | Feature weighted models to address lineage dependency in drug-resistance prediction from Mycobacterium tuberculosis genome sequences |
title_full_unstemmed | Feature weighted models to address lineage dependency in drug-resistance prediction from Mycobacterium tuberculosis genome sequences |
title_short | Feature weighted models to address lineage dependency in drug-resistance prediction from Mycobacterium tuberculosis genome sequences |
title_sort | feature weighted models to address lineage dependency in drug-resistance prediction from mycobacterium tuberculosis genome sequences |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10351970/ https://www.ncbi.nlm.nih.gov/pubmed/37428143 http://dx.doi.org/10.1093/bioinformatics/btad428 |
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