Robust computational analysis of rRNA hypervariable tag datasets.

Next-generation DNA sequencing is increasingly being utilized to probe microbial communities, such as gastrointestinal microbiomes, where it is important to be able to quantify measures of abundance and diversity. The fragmented nature of the 16S rRNA datasets obtained, coupled with their unpreceden...

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Main Authors: Maksim Sipos, Patricio Jeraldo, Nicholas Chia, Ani Qu, A Singh Dhillon, Michael E Konkel, Karen E Nelson, Bryan A White, Nigel Goldenfeld
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3013109?pdf=render
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spelling doaj-e28836e2814343adb6eb8f68a81a339b2020-11-25T02:00:17ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-01-01512e1522010.1371/journal.pone.0015220Robust computational analysis of rRNA hypervariable tag datasets.Maksim SiposPatricio JeraldoNicholas ChiaAni QuA Singh DhillonMichael E KonkelKaren E NelsonBryan A WhiteNigel GoldenfeldNext-generation DNA sequencing is increasingly being utilized to probe microbial communities, such as gastrointestinal microbiomes, where it is important to be able to quantify measures of abundance and diversity. The fragmented nature of the 16S rRNA datasets obtained, coupled with their unprecedented size, has led to the recognition that the results of such analyses are potentially contaminated by a variety of artifacts, both experimental and computational. Here we quantify how multiple alignment and clustering errors contribute to overestimates of abundance and diversity, reflected by incorrect OTU assignment, corrupted phylogenies, inaccurate species diversity estimators, and rank abundance distribution functions. We show that straightforward procedural optimizations, combining preexisting tools, are effective in handling large (10(5)-10(6)) 16S rRNA datasets, and we describe metrics to measure the effectiveness and quality of the estimators obtained. We introduce two metrics to ascertain the quality of clustering of pyrosequenced rRNA data, and show that complete linkage clustering greatly outperforms other widely used methods.http://europepmc.org/articles/PMC3013109?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Maksim Sipos
Patricio Jeraldo
Nicholas Chia
Ani Qu
A Singh Dhillon
Michael E Konkel
Karen E Nelson
Bryan A White
Nigel Goldenfeld
spellingShingle Maksim Sipos
Patricio Jeraldo
Nicholas Chia
Ani Qu
A Singh Dhillon
Michael E Konkel
Karen E Nelson
Bryan A White
Nigel Goldenfeld
Robust computational analysis of rRNA hypervariable tag datasets.
PLoS ONE
author_facet Maksim Sipos
Patricio Jeraldo
Nicholas Chia
Ani Qu
A Singh Dhillon
Michael E Konkel
Karen E Nelson
Bryan A White
Nigel Goldenfeld
author_sort Maksim Sipos
title Robust computational analysis of rRNA hypervariable tag datasets.
title_short Robust computational analysis of rRNA hypervariable tag datasets.
title_full Robust computational analysis of rRNA hypervariable tag datasets.
title_fullStr Robust computational analysis of rRNA hypervariable tag datasets.
title_full_unstemmed Robust computational analysis of rRNA hypervariable tag datasets.
title_sort robust computational analysis of rrna hypervariable tag datasets.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2010-01-01
description Next-generation DNA sequencing is increasingly being utilized to probe microbial communities, such as gastrointestinal microbiomes, where it is important to be able to quantify measures of abundance and diversity. The fragmented nature of the 16S rRNA datasets obtained, coupled with their unprecedented size, has led to the recognition that the results of such analyses are potentially contaminated by a variety of artifacts, both experimental and computational. Here we quantify how multiple alignment and clustering errors contribute to overestimates of abundance and diversity, reflected by incorrect OTU assignment, corrupted phylogenies, inaccurate species diversity estimators, and rank abundance distribution functions. We show that straightforward procedural optimizations, combining preexisting tools, are effective in handling large (10(5)-10(6)) 16S rRNA datasets, and we describe metrics to measure the effectiveness and quality of the estimators obtained. We introduce two metrics to ascertain the quality of clustering of pyrosequenced rRNA data, and show that complete linkage clustering greatly outperforms other widely used methods.
url http://europepmc.org/articles/PMC3013109?pdf=render
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