Evidence map›Paper›PMID 30887686›Full record

ArticleMolecular ecology resources2019

Laboratory contamination over time during low-biomass sample analysis.

Laura S Weyrich, Andrew G Farrer, Raphael Eisenhofer, Luis A Arriola, Jennifer Young, Caitlin A Selway, Matilda Handsley-Davis, Christina J Adler, James Breen, Alan Cooper

Abstract read
In one paragraph

Article in Molecular ecology resources, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 131 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
131citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

131 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Metagenomic Data Preprocessing and Quality Control.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

71 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Laura S WeyrichAustralian Centre for Ancient DNA, University of Adelaide, Adelaide, South Australia, Australia.ORCID https://orcid.org/0000-0001-5243-4634
Andrew G FarrerAustralian Centre for Ancient DNA, University of Adelaide, Adelaide, South Australia, Australia.
Raphael EisenhoferAustralian Centre for Ancient DNA, University of Adelaide, Adelaide, South Australia, Australia.
Luis A ArriolaAustralian Centre for Ancient DNA, University of Adelaide, Adelaide, South Australia, Australia.
Jennifer YoungAustralian Centre for Ancient DNA, University of Adelaide, Adelaide, South Australia, Australia.
Caitlin A SelwayAustralian Centre for Ancient DNA, University of Adelaide, Adelaide, South Australia, Australia.
Matilda Handsley-DavisAustralian Centre for Ancient DNA, University of Adelaide, Adelaide, South Australia, Australia.
Christina J AdlerSchool of Dentistry, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.
James BreenAustralian Centre for Ancient DNA, University of Adelaide, Adelaide, South Australia, Australia.
Alan CooperAustralian Centre for Ancient DNA, University of Adelaide, Adelaide, South Australia, Australia.

Funding

Australian Research Council DECRA 150101574
6 · The paper itself

Abstract

Bacteria are not only ubiquitous on earth but can also be incredibly diverse within clean laboratories and reagents. The presence of both living and dead bacteria in laboratory environments and reagents is especially problematic when examining samples with low endogenous content (e.g., skin swabs, tissue biopsies, ice, water, degraded forensic samples or ancient material), where contaminants can outnumber endogenous microorganisms within samples. The contribution of contaminants within high-throughput studies remains poorly understood because of the relatively low number of contaminant surveys. Here, we examined 144 negative control samples (extraction blank and no-template amplification controls) collected in both typical molecular laboratories and an ultraclean ancient DNA laboratory over 5 years to characterize long-term contaminant diversity. We additionally compared the contaminant content within a home-made silica-based extraction method, commonly used to analyse low endogenous content samples, with a widely used commercial DNA extraction kit. The contaminant taxonomic profile of the ultraclean ancient DNA laboratory was unique compared to modern molecular biology laboratories, and changed over time according to researcher, month and season. The commercial kit also contained higher microbial diversity and several human-associated taxa in comparison to the home-made silica extraction protocol. We recommend a minimum of two strategies to reduce the impacts of laboratory contaminants within low-biomass metagenomic studies: (a) extraction blank controls should be included and sequenced with every batch of extractions and (b) the contributions of laboratory contamination should be assessed and reported in each high-throughput metagenomic study.

Indexed as

Diagnostic ErrorsDNA ContaminationMetagenomicsMolecular Biologyancient DNAcontaminantcontaminationmetagenomicsmicrobiomemicrobiota

Identifiers

PMID30887686
PMCPMC6850301

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.