Evidence map›Paper›PMID 23387433›Full record

ArticleBMC bioinformatics2013

M-pick, a modularity-based method for OTU picking of 16S rRNA sequences.

Xiaoyu Wang, Jin Yao, Yijun Sun, Volker Mai

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Article in BMC bioinformatics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

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14citing papers in PubMed
–field-weighted citation impact
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3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. A clinician's guide to microbiome analysis.Nature reviews. Gastroenterology & hepatology · 2017
    Review
  7. Article
  8. High-resolution characterization of the human microbiome.Translational research : the journal of laboratory and clinical medicine · 2017
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Phylogenetics and the human microbiome.Systematic biology · 2015
    Review
  14. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xiaoyu WangDepartment of Epidemiology, College of Public Health and Health Professions and College of Medicine, Emerging Pathogens Institute, University of Florida, Gainesville, FL 32610, USA.
Jin Yao
Yijun Sun
Volker Mai

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBinning 16S rRNA sequences into operational taxonomic units (OTUs) is an initial crucial step in analyzing large sequence datasets generated to determine microbial community compositions in various environments including that of the human gut. Various methods have been developed, but most suffer from either inaccuracies or from being unable to handle millions of sequences generated in current studies. Furthermore, existing binning methods usually require a priori decisions regarding binning parameters such as a distance level for defining an OTU.

resultsWe present a novel modularity-based approach (M-pick) to address the aforementioned problems. The new method utilizes ideas from community detection in graphs, where sequences are viewed as vertices on a weighted graph, each pair of sequences is connected by an imaginary edge, and the similarity of a pair of sequences represents the weight of the edge. M-pick first generates a graph based on pairwise sequence distances and then applies a modularity-based community detection technique on the graph to generate OTUs to capture the community structures in sequence data. To compare the performance of M-pick with that of existing methods, specifically CROP and ESPRIT-Tree, sequence data from different hypervariable regions of 16S rRNA were used and binning results were compared.

conclusionsA new modularity-based clustering method for OTU picking of 16S rRNA sequences is developed in this study. The algorithm does not require a predetermined cut-off level, and our simulation studies suggest that it is superior to existing methods that require specified distance levels to define OTUs. The source code is available at http://plaza.ufl.edu/xywang/Mpick.htm.

Indexed as

AlgorithmsClassificationCluster AnalysisGastrointestinal TractGenetic VariationHumansRNA, Ribosomal, 16SSequence Analysis, DNARNA, Ribosomal, 16S

Identifiers

PMID23387433
PMCPMC3599145

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LicenceCC BY
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.