Evidence map›Paper›PMID 31936690›Full record

ArticleGenes2020

Off Earth Identification of Bacterial Populations Using 16S rDNA Nanopore Sequencing.

Aaron S Burton, Sarah E Stahl, Kristen K John, Miten Jain, Sissel Juul, Daniel J Turner, Eoghan D Harrington, David Stoddart, Benedict Paten, Mark Akeson and 1 more

Open access · goldAbstract read
In one paragraph

Article in Genes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.9field-weighted citation impact, top 4% of its field
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

30 citing papers in PubMed, 57 citations in OpenAlex.

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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

11 authors at 5 institutions in 2 countries.

Aaron S BurtonAstromaterials Research and Exploration Science Division, NASA Johnson Space Center, Houston, TX 77058, USA.ORCID 0000-0002-1194-4336
Sarah E StahlJES Tech, Houston, TX 77058, USA.
Kristen K JohnJacobs Engineering Group Inc., Houston, TX 77058, USA.
Miten JainUCSC Genomics Institute, University of California, Santa Cruz, CA 95064, USA.ORCID 0000-0002-4571-3982
Sissel JuulOxford Nanopore Technologies, New York, NY 10013, USA.ORCID 0000-0002-0315-4449
Daniel J TurnerOxford Nanopore Technologies, Oxford Science Park, Oxford OX4 4DQ, UK.
Eoghan D HarringtonOxford Nanopore Technologies, New York, NY 10013, USA.
David StoddartOxford Nanopore Technologies, Oxford Science Park, Oxford OX4 4DQ, UK.
Benedict PatenUCSC Genomics Institute, University of California, Santa Cruz, CA 95064, USA.
Mark AkesonUCSC Genomics Institute, University of California, Santa Cruz, CA 95064, USA.
Sarah L Castro-WallaceBiomedical Research and Environmental Sciences Division, NASA Johnson Space Center, Houston, TX 77058, USA.
University of California, Santa Cruz · USJohnson Space Center · USOxford Nanopore Technologies (United Kingdom) · GBJacobs (United States) · USJES Tech (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The MinION sequencer has made in situ sequencing feasible in remote locations. Following our initial demonstration of its high performance off planet with Earth-prepared samples, we developed and tested an end-to-end, sample-to-sequencer process that could be conducted entirely aboard the International Space Station (ISS). Initial experiments demonstrated the process with a microbial mock community standard. The DNA was successfully amplified, primers were degraded, and libraries prepared and sequenced. The median percent identities for both datasets were 84%, as assessed from alignment of the mock community. The ability to correctly identify the organisms in the mock community standard was comparable for the sequencing data obtained in flight and on the ground. To validate the process on microbes collected from and cultured aboard the ISS, bacterial cells were selected from a NASA Environmental Health Systems Surface Sample Kit contact slide. The locations of bacterial colonies chosen for identification were labeled, and a small number of cells were directly added as input into the sequencing workflow. Prepared DNA was sequenced, and the data were downlinked to Earth. Return of the contact slide to the ground allowed for standard laboratory processing for bacterial identification. The identifications obtained aboard the ISS,

Indexed as

BacteriaDNA, BacterialDNA, RibosomalExobiologyExtraterrestrial EnvironmentGenome, BacterialMicrobiotaNanoporesNanopore SequencingRNA, Ribosomal, 16SSequence Analysis, DNASpacecraftSpecimen HandlingDNA, BacterialDNA, RibosomalRNA, Ribosomal, 16Sbacterial identificationfield-deployable methodsin situ analysisnanopore sequencingspaceflight

Identifiers

PMID31936690
PMCPMC7016637
OpenAlexW3000173032

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.