Evidence map›Paper›PMID 37938281›Full record

ArticleISME communications2021

Microvolume DNA extraction methods for microscale amplicon and metagenomic studies.

Anna R Bramucci, Amaranta Focardi, Christian Rinke, Philip Hugenholtz, Gene W Tyson, Justin R Seymour, Jean-Baptiste Raina

Abstract read
In one paragraph

Article in ISME communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–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

20 citing papers in PubMed.

  1. Article
  2. Quantitative metagenomics using a portable protocol.Applied and environmental microbiology · 2026
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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

7 authors.

Anna R BramucciClimate Change Cluster (C3), University of Technology Sydney, Sydney, NSW, 2007, Australia.
Amaranta FocardiClimate Change Cluster (C3), University of Technology Sydney, Sydney, NSW, 2007, Australia.
Christian RinkeAustralian Centre for Ecogenomics, School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Philip HugenholtzAustralian Centre for Ecogenomics, School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Gene W TysonCentre for Microbiome Research, School of Biomedical Sciences, Queensland University of Technology, Translational Research Institute, Brisbane, QLD, 4102, Australia.
Justin R SeymourClimate Change Cluster (C3), University of Technology Sydney, Sydney, NSW, 2007, Australia.
Jean-Baptiste RainaClimate Change Cluster (C3), University of Technology Sydney, Sydney, NSW, 2007, Australia. Jean-Baptiste.Raina@uts.edu.au.

Funding

Department of Education and Training | Australian Research Council (ARC) DP180100838Department of Education and Training | Australian Research Council (ARC) DP200100919
6 · The paper itself

Abstract

Investigating the composition and metabolic capacity of aquatic microbial assemblages usually requires the filtration of multi-litre samples, which are up to 1 million-fold larger than the microenvironments within which microbes are predicted to be spatially organised. To determine if community profiles can be reliably generated from microlitre volumes, we sampled seawater at a coastal and an oceanic site, filtered and homogenised them, and extracted DNA from bulk samples (2 L) and microvolumes (100, 10 and 1 μL) using two new approaches. These microvolume DNA extraction methods involve either physical or chemical lysis (through pH/thermal shock and lytic enzymes/surfactants, respectively), directly followed by the capture of DNA on magnetic beads. Downstream analysis of extracted DNA using both amplicon sequencing and metagenomics, revealed strong correlation with standard large volume approaches, demonstrating the fidelity of taxonomic and functional profiles of microbial communities in as little as 1 μL of seawater. This volume is six orders of magnitude smaller than most standard operating procedures for marine metagenomics, which will allow precise sampling of the heterogenous landscape that microbes inhabit.

Identifiers

PMID37938281
PMCPMC9723667

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Registered trials

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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.