posted on 2025-05-09, 14:40authored bySimon A. Hardwick, Wendy Y. Chen, Catherine E. Lovelock, Brett NeilanBrett Neilan, Tim R. Mercer, Ted Wong, Bindu S. Kanakamedala, Ira W. Deveson, Sarah E. Ongley, Nadia S. Santini, Esteban Marcellin, Martin A. Smith, Lars K. Nielsen
The complexity of microbial communities, combined with technical biases in next-generation sequencing, pose a challenge to metagenomic analysis. Here, we develop a set of internal DNA standards, termed “sequins” (sequencing spike-ins), that together constitute a synthetic community of artificial microbial genomes. Sequins are added to environmental DNA samples prior to library preparation, and undergo concurrent sequencing with the accompanying sample. We validate the performance of sequins by comparison to mock microbial communities, and demonstrate their use in the analysis of real metagenome samples. We show how sequins can be used to measure fold change differences in the size and structure of accompanying microbial communities, and perform quantitative normalization between samples. We further illustrate how sequins can be used to benchmark and optimize new methods, including nanopore long-read sequencing technology. We provide metagenome sequins, along with associated data sets, protocols, and an accompanying software toolkit, as reference standards to aid in metagenomic studies.
Funding
NHMRC
1062470
History
Journal title
Nature Communication
Volume
9
Article number
3096
Publisher
Nature Publishing Group
Language
en, English
College/Research Centre
Faculty of Science
School
School of Environmental and Life Sciences
Rights statement
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