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GAMBIT (Genomic Approximation Method for Bacterial Identification and Tracking): A methodology to rapidly leverage whole genome sequencing of bacterial isolates for clinical identification
Whole genome sequencing (WGS) of clinical bacterial isolates has the potential to transform the fields of diagnostics and public health. To realize this potential, bioinformatic software that reports identification results needs to be developed that meets the quality standards of a diagnostic test....
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934365/ https://www.ncbi.nlm.nih.gov/pubmed/36795668 http://dx.doi.org/10.1371/journal.pone.0277575 |
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author | Lumpe, Jared Gumbleton, Lynette Gorzalski, Andrew Libuit, Kevin Varghese, Vici Lloyd, Tyler Tadros, Farid Arsimendi, Tyler Wagner, Eileen Stephens, Craig Sevinsky, Joel Hess, David Pandori, Mark |
author_facet | Lumpe, Jared Gumbleton, Lynette Gorzalski, Andrew Libuit, Kevin Varghese, Vici Lloyd, Tyler Tadros, Farid Arsimendi, Tyler Wagner, Eileen Stephens, Craig Sevinsky, Joel Hess, David Pandori, Mark |
author_sort | Lumpe, Jared |
collection | PubMed |
description | Whole genome sequencing (WGS) of clinical bacterial isolates has the potential to transform the fields of diagnostics and public health. To realize this potential, bioinformatic software that reports identification results needs to be developed that meets the quality standards of a diagnostic test. We developed GAMBIT (Genomic Approximation Method for Bacterial Identification and Tracking) using k-mer based strategies for identification of bacteria based on WGS reads. GAMBIT incorporates this algorithm with a highly curated searchable database of 48,224 genomes. Herein, we describe validation of the scoring methodology, parameter robustness, establishment of confidence thresholds and the curation of the reference database. We assessed GAMBIT by way of validation studies when it was deployed as a laboratory-developed test in two public health laboratories. This method greatly reduces or eliminates false identifications which are often detrimental in a clinical setting. |
format | Online Article Text |
id | pubmed-9934365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-99343652023-02-17 GAMBIT (Genomic Approximation Method for Bacterial Identification and Tracking): A methodology to rapidly leverage whole genome sequencing of bacterial isolates for clinical identification Lumpe, Jared Gumbleton, Lynette Gorzalski, Andrew Libuit, Kevin Varghese, Vici Lloyd, Tyler Tadros, Farid Arsimendi, Tyler Wagner, Eileen Stephens, Craig Sevinsky, Joel Hess, David Pandori, Mark PLoS One Research Article Whole genome sequencing (WGS) of clinical bacterial isolates has the potential to transform the fields of diagnostics and public health. To realize this potential, bioinformatic software that reports identification results needs to be developed that meets the quality standards of a diagnostic test. We developed GAMBIT (Genomic Approximation Method for Bacterial Identification and Tracking) using k-mer based strategies for identification of bacteria based on WGS reads. GAMBIT incorporates this algorithm with a highly curated searchable database of 48,224 genomes. Herein, we describe validation of the scoring methodology, parameter robustness, establishment of confidence thresholds and the curation of the reference database. We assessed GAMBIT by way of validation studies when it was deployed as a laboratory-developed test in two public health laboratories. This method greatly reduces or eliminates false identifications which are often detrimental in a clinical setting. Public Library of Science 2023-02-16 /pmc/articles/PMC9934365/ /pubmed/36795668 http://dx.doi.org/10.1371/journal.pone.0277575 Text en © 2023 Lumpe et al 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 use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lumpe, Jared Gumbleton, Lynette Gorzalski, Andrew Libuit, Kevin Varghese, Vici Lloyd, Tyler Tadros, Farid Arsimendi, Tyler Wagner, Eileen Stephens, Craig Sevinsky, Joel Hess, David Pandori, Mark GAMBIT (Genomic Approximation Method for Bacterial Identification and Tracking): A methodology to rapidly leverage whole genome sequencing of bacterial isolates for clinical identification |
title | GAMBIT (Genomic Approximation Method for Bacterial Identification and Tracking): A methodology to rapidly leverage whole genome sequencing of bacterial isolates for clinical identification |
title_full | GAMBIT (Genomic Approximation Method for Bacterial Identification and Tracking): A methodology to rapidly leverage whole genome sequencing of bacterial isolates for clinical identification |
title_fullStr | GAMBIT (Genomic Approximation Method for Bacterial Identification and Tracking): A methodology to rapidly leverage whole genome sequencing of bacterial isolates for clinical identification |
title_full_unstemmed | GAMBIT (Genomic Approximation Method for Bacterial Identification and Tracking): A methodology to rapidly leverage whole genome sequencing of bacterial isolates for clinical identification |
title_short | GAMBIT (Genomic Approximation Method for Bacterial Identification and Tracking): A methodology to rapidly leverage whole genome sequencing of bacterial isolates for clinical identification |
title_sort | gambit (genomic approximation method for bacterial identification and tracking): a methodology to rapidly leverage whole genome sequencing of bacterial isolates for clinical identification |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9934365/ https://www.ncbi.nlm.nih.gov/pubmed/36795668 http://dx.doi.org/10.1371/journal.pone.0277575 |
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