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Libra: scalable k-mer–based tool for massive all-vs-all metagenome comparisons
BACKGROUND: Shotgun metagenomics provides powerful insights into microbial community biodiversity and function. Yet, inferences from metagenomic studies are often limited by dataset size and complexity and are restricted by the availability and completeness of existing databases. De novo comparative...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354030/ https://www.ncbi.nlm.nih.gov/pubmed/30597002 http://dx.doi.org/10.1093/gigascience/giy165 |
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author | Choi, Illyoung Ponsero, Alise J Bomhoff, Matthew Youens-Clark, Ken Hartman, John H Hurwitz, Bonnie L |
author_facet | Choi, Illyoung Ponsero, Alise J Bomhoff, Matthew Youens-Clark, Ken Hartman, John H Hurwitz, Bonnie L |
author_sort | Choi, Illyoung |
collection | PubMed |
description | BACKGROUND: Shotgun metagenomics provides powerful insights into microbial community biodiversity and function. Yet, inferences from metagenomic studies are often limited by dataset size and complexity and are restricted by the availability and completeness of existing databases. De novo comparative metagenomics enables the comparison of metagenomes based on their total genetic content. RESULTS: We developed a tool called Libra that performs an all-vs-all comparison of metagenomes for precise clustering based on their k-mer content. Libra uses a scalable Hadoop framework for massive metagenome comparisons, Cosine Similarity for calculating the distance using sequence composition and abundance while normalizing for sequencing depth, and a web-based implementation in iMicrobe (http://imicrobe.us) that uses the CyVerse advanced cyberinfrastructure to promote broad use of the tool by the scientific community. CONCLUSIONS: A comparison of Libra to equivalent tools using both simulated and real metagenomic datasets, ranging from 80 million to 4.2 billion reads, reveals that methods commonly implemented to reduce compute time for large datasets, such as data reduction, read count normalization, and presence/absence distance metrics, greatly diminish the resolution of large-scale comparative analyses. In contrast, Libra uses all of the reads to calculate k-mer abundance in a Hadoop architecture that can scale to any size dataset to enable global-scale analyses and link microbial signatures to biological processes. |
format | Online Article Text |
id | pubmed-6354030 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63540302019-02-05 Libra: scalable k-mer–based tool for massive all-vs-all metagenome comparisons Choi, Illyoung Ponsero, Alise J Bomhoff, Matthew Youens-Clark, Ken Hartman, John H Hurwitz, Bonnie L Gigascience Technical Note BACKGROUND: Shotgun metagenomics provides powerful insights into microbial community biodiversity and function. Yet, inferences from metagenomic studies are often limited by dataset size and complexity and are restricted by the availability and completeness of existing databases. De novo comparative metagenomics enables the comparison of metagenomes based on their total genetic content. RESULTS: We developed a tool called Libra that performs an all-vs-all comparison of metagenomes for precise clustering based on their k-mer content. Libra uses a scalable Hadoop framework for massive metagenome comparisons, Cosine Similarity for calculating the distance using sequence composition and abundance while normalizing for sequencing depth, and a web-based implementation in iMicrobe (http://imicrobe.us) that uses the CyVerse advanced cyberinfrastructure to promote broad use of the tool by the scientific community. CONCLUSIONS: A comparison of Libra to equivalent tools using both simulated and real metagenomic datasets, ranging from 80 million to 4.2 billion reads, reveals that methods commonly implemented to reduce compute time for large datasets, such as data reduction, read count normalization, and presence/absence distance metrics, greatly diminish the resolution of large-scale comparative analyses. In contrast, Libra uses all of the reads to calculate k-mer abundance in a Hadoop architecture that can scale to any size dataset to enable global-scale analyses and link microbial signatures to biological processes. Oxford University Press 2018-12-28 /pmc/articles/PMC6354030/ /pubmed/30597002 http://dx.doi.org/10.1093/gigascience/giy165 Text en © The Author(s) 2018. Published by Oxford University Press. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Technical Note Choi, Illyoung Ponsero, Alise J Bomhoff, Matthew Youens-Clark, Ken Hartman, John H Hurwitz, Bonnie L Libra: scalable k-mer–based tool for massive all-vs-all metagenome comparisons |
title | Libra: scalable k-mer–based tool for massive all-vs-all metagenome comparisons |
title_full | Libra: scalable k-mer–based tool for massive all-vs-all metagenome comparisons |
title_fullStr | Libra: scalable k-mer–based tool for massive all-vs-all metagenome comparisons |
title_full_unstemmed | Libra: scalable k-mer–based tool for massive all-vs-all metagenome comparisons |
title_short | Libra: scalable k-mer–based tool for massive all-vs-all metagenome comparisons |
title_sort | libra: scalable k-mer–based tool for massive all-vs-all metagenome comparisons |
topic | Technical Note |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6354030/ https://www.ncbi.nlm.nih.gov/pubmed/30597002 http://dx.doi.org/10.1093/gigascience/giy165 |
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