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Full-Length Envelope Analyzer (FLEA): A tool for longitudinal analysis of viral amplicons
Next generation sequencing of viral populations has advanced our understanding of viral population dynamics, the development of drug resistance, and escape from host immune responses. Many applications require complete gene sequences, which can be impossible to reconstruct from short reads. HIV env,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6314628/ https://www.ncbi.nlm.nih.gov/pubmed/30543621 http://dx.doi.org/10.1371/journal.pcbi.1006498 |
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author | Eren, Kemal Weaver, Steven Ketteringham, Robert Valentyn, Morné Laird Smith, Melissa Kumar, Venkatesh Mohan, Sanjay Kosakovsky Pond, Sergei L. Murrell, Ben |
author_facet | Eren, Kemal Weaver, Steven Ketteringham, Robert Valentyn, Morné Laird Smith, Melissa Kumar, Venkatesh Mohan, Sanjay Kosakovsky Pond, Sergei L. Murrell, Ben |
author_sort | Eren, Kemal |
collection | PubMed |
description | Next generation sequencing of viral populations has advanced our understanding of viral population dynamics, the development of drug resistance, and escape from host immune responses. Many applications require complete gene sequences, which can be impossible to reconstruct from short reads. HIV env, the protein of interest for HIV vaccine studies, is exceptionally challenging for long-read sequencing and analysis due to its length, high substitution rate, and extensive indel variation. While long-read sequencing is attractive in this setting, the analysis of such data is not well handled by existing methods. To address this, we introduce FLEA (Full-Length Envelope Analyzer), which performs end-to-end analysis and visualization of long-read sequencing data. FLEA consists of both a pipeline (optionally run on a high-performance cluster), and a client-side web application that provides interactive results. The pipeline transforms FASTQ reads into high-quality consensus sequences (HQCSs) and uses them to build a codon-aware multiple sequence alignment. The resulting alignment is then used to infer phylogenies, selection pressure, and evolutionary dynamics. The web application provides publication-quality plots and interactive visualizations, including an annotated viral alignment browser, time series plots of evolutionary dynamics, visualizations of gene-wide selective pressures (such as dN/dS) across time and across protein structure, and a phylogenetic tree browser. We demonstrate how FLEA may be used to process Pacific Biosciences HIV env data and describe recent examples of its use. Simulations show how FLEA dramatically reduces the error rate of this sequencing platform, providing an accurate portrait of complex and variable HIV env populations. A public instance of FLEA is hosted at http://flea.datamonkey.org. The Python source code for the FLEA pipeline can be found at https://github.com/veg/flea-pipeline. The client-side application is available at https://github.com/veg/flea-web-app. A live demo of the P018 results can be found at http://flea.murrell.group/view/P018. |
format | Online Article Text |
id | pubmed-6314628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-63146282019-01-11 Full-Length Envelope Analyzer (FLEA): A tool for longitudinal analysis of viral amplicons Eren, Kemal Weaver, Steven Ketteringham, Robert Valentyn, Morné Laird Smith, Melissa Kumar, Venkatesh Mohan, Sanjay Kosakovsky Pond, Sergei L. Murrell, Ben PLoS Comput Biol Research Article Next generation sequencing of viral populations has advanced our understanding of viral population dynamics, the development of drug resistance, and escape from host immune responses. Many applications require complete gene sequences, which can be impossible to reconstruct from short reads. HIV env, the protein of interest for HIV vaccine studies, is exceptionally challenging for long-read sequencing and analysis due to its length, high substitution rate, and extensive indel variation. While long-read sequencing is attractive in this setting, the analysis of such data is not well handled by existing methods. To address this, we introduce FLEA (Full-Length Envelope Analyzer), which performs end-to-end analysis and visualization of long-read sequencing data. FLEA consists of both a pipeline (optionally run on a high-performance cluster), and a client-side web application that provides interactive results. The pipeline transforms FASTQ reads into high-quality consensus sequences (HQCSs) and uses them to build a codon-aware multiple sequence alignment. The resulting alignment is then used to infer phylogenies, selection pressure, and evolutionary dynamics. The web application provides publication-quality plots and interactive visualizations, including an annotated viral alignment browser, time series plots of evolutionary dynamics, visualizations of gene-wide selective pressures (such as dN/dS) across time and across protein structure, and a phylogenetic tree browser. We demonstrate how FLEA may be used to process Pacific Biosciences HIV env data and describe recent examples of its use. Simulations show how FLEA dramatically reduces the error rate of this sequencing platform, providing an accurate portrait of complex and variable HIV env populations. A public instance of FLEA is hosted at http://flea.datamonkey.org. The Python source code for the FLEA pipeline can be found at https://github.com/veg/flea-pipeline. The client-side application is available at https://github.com/veg/flea-web-app. A live demo of the P018 results can be found at http://flea.murrell.group/view/P018. Public Library of Science 2018-12-13 /pmc/articles/PMC6314628/ /pubmed/30543621 http://dx.doi.org/10.1371/journal.pcbi.1006498 Text en © 2018 Eren et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://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 Eren, Kemal Weaver, Steven Ketteringham, Robert Valentyn, Morné Laird Smith, Melissa Kumar, Venkatesh Mohan, Sanjay Kosakovsky Pond, Sergei L. Murrell, Ben Full-Length Envelope Analyzer (FLEA): A tool for longitudinal analysis of viral amplicons |
title | Full-Length Envelope Analyzer (FLEA): A tool for longitudinal analysis of viral amplicons |
title_full | Full-Length Envelope Analyzer (FLEA): A tool for longitudinal analysis of viral amplicons |
title_fullStr | Full-Length Envelope Analyzer (FLEA): A tool for longitudinal analysis of viral amplicons |
title_full_unstemmed | Full-Length Envelope Analyzer (FLEA): A tool for longitudinal analysis of viral amplicons |
title_short | Full-Length Envelope Analyzer (FLEA): A tool for longitudinal analysis of viral amplicons |
title_sort | full-length envelope analyzer (flea): a tool for longitudinal analysis of viral amplicons |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6314628/ https://www.ncbi.nlm.nih.gov/pubmed/30543621 http://dx.doi.org/10.1371/journal.pcbi.1006498 |
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