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Biodiversity Soup II: A bulk-sample metabarcoding pipeline emphasizing error reduction

Yang, C, Bohmann, K, Wang, X, Cai, W, Wales, N, Ding, Z, Gopalakrishnan, S and Yu, DW (2021) Biodiversity Soup II: A bulk-sample metabarcoding pipeline emphasizing error reduction. Methods in Ecology and Evolution, 12 (7). pp. 1252-1264. ISSN 2041-210X

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Open Access URL: https://doi.org/10.1111/2041-210X.13602 (Published version)


Despite widespread recognition of its great promise to aid decision-making in environmental management, the applied use of metabarcoding requires improvements to reduce the multiple errors that arise during PCR amplification, sequencing and library generation. We present a co-designed wet-lab and bioinformatic workflow for metabarcoding bulk samples that removes both false-positive (tag jumps, chimeras, erroneous sequences) and false-negative (‘dropout’) errors. However, we find that it is not possible to recover relative-abundance information from amplicon data, due to persistent species-specific biases. To present and validate our workflow, we created eight mock arthropod soups, all containing the same 248 arthropod morphospecies but differing in absolute and relative DNA concentrations, and we ran them under five different PCR conditions. Our pipeline includes qPCR-optimized PCR annealing temperature and cycle number, twin-tagging, multiple independent PCR replicates per sample, and negative and positive controls. In the bioinformatic portion, we introduce Begum, which is a new version of DAMe (Zepeda-Mendoza et al., 2016. BMC Res. Notes 9:255) that ignores heterogeneity spacers, allows primer mismatches when demultiplexing samples and is more efficient. Like DAMe, Begum removes tag-jumped reads and removes sequence errors by keeping only sequences that appear in more than one PCR above a minimum copy number per PCR. The filtering thresholds are user-configurable. We report that OTU dropout frequency and taxonomic amplification bias are both reduced by using a PCR annealing temperature and cycle number on the low ends of the ranges currently used for the Leray-FolDegenRev primers. We also report that tag jumps and erroneous sequences can be nearly eliminated with Begum filtering, at the cost of only a small rise in dropouts. We replicate published findings that uneven size distribution of input biomasses leads to greater dropout frequency and that OTU size is a poor predictor of species input biomass. Finally, we find no evidence for ‘tag-biased’ PCR amplification. To aid learning, reproducibility, and the design and testing of alternative metabarcoding pipelines, we provide our Illumina and input-species sequence datasets, scripts, a spreadsheet for designing primer tags and a tutorial.

Item Type: Article
Uncontrolled Keywords: ARTHROPODS; BIAS; bulk‐ DIET; DIVERSITY; Ecology; environmental DNA; ENVIRONMENTAL DNA; environmental impact assessment; Environmental Sciences & Ecology; false negatives; false positives; Illumina high‐ Life Sciences & Biomedicine; PCR; sample DNA metabarcoding; Science & Technology; tag bias; throughput sequencing; Science & Technology; Life Sciences & Biomedicine; Ecology; Environmental Sciences & Ecology; bulk‐ sample DNA metabarcoding; environmental DNA; environmental impact assessment; false negatives; false positives; Illumina high‐ throughput sequencing; tag bias; ENVIRONMENTAL DNA; DIVERSITY; ARTHROPODS; DIET; BIAS; PCR; 0502 Environmental Science and Management; 0602 Ecology; 0603 Evolutionary Biology
Subjects: Q Science > QH Natural history > QH301 Biology
Divisions: Biological & Environmental Sciences (from Sep 19)
Publisher: Wiley
SWORD Depositor: A Symplectic
Date Deposited: 07 Oct 2022 11:41
Last Modified: 07 Oct 2022 11:45
DOI or ID number: 10.1111/2041-210X.13602
URI: https://researchonline.ljmu.ac.uk/id/eprint/17754
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