Evidence map›Paper›PMID 36765984›Full record

ArticleFoods (Basel, Switzerland)2023

Targeted High-Throughput Sequencing Enables the Detection of Single Nucleotide Variations in CRISPR/Cas9 Gene-Edited Organisms.

Marie-Alice Fraiture, Jolien D'aes, Emmanuel Guiderdoni, Anne-Cécile Meunier, Thomas Delcourt, Stefan Hoffman, Els Vandermassen, Sigrid C J De Keersmaecker, Kevin Vanneste, Nancy H C Roosens

Abstract read
In one paragraph

Article in Foods (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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  3. Review
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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

10 authors.

Marie-Alice FraitureSciensano, Transversal Activities in Applied Genomics (TAG), rue Juliette Wytsman 14, 1050 Brussels, Belgium.ORCID 0000-0002-2527-1785
Jolien D'aesSciensano, Transversal Activities in Applied Genomics (TAG), rue Juliette Wytsman 14, 1050 Brussels, Belgium.ORCID 0000-0001-7687-3105
Emmanuel GuiderdoniCIRAD, UMR AGAP Institut, F-34398 Montpellier, France.ORCID 0000-0003-2760-2864
Anne-Cécile MeunierCIRAD, UMR AGAP Institut, F-34398 Montpellier, France.
Thomas DelcourtSciensano, Transversal Activities in Applied Genomics (TAG), rue Juliette Wytsman 14, 1050 Brussels, Belgium.ORCID 0000-0003-1690-1957
Stefan HoffmanSciensano, Transversal Activities in Applied Genomics (TAG), rue Juliette Wytsman 14, 1050 Brussels, Belgium.
Els VandermassenSciensano, Transversal Activities in Applied Genomics (TAG), rue Juliette Wytsman 14, 1050 Brussels, Belgium.
Sigrid C J De KeersmaeckerSciensano, Transversal Activities in Applied Genomics (TAG), rue Juliette Wytsman 14, 1050 Brussels, Belgium.ORCID 0000-0003-4198-4133
Kevin VannesteSciensano, Transversal Activities in Applied Genomics (TAG), rue Juliette Wytsman 14, 1050 Brussels, Belgium.
Nancy H C RoosensSciensano, Transversal Activities in Applied Genomics (TAG), rue Juliette Wytsman 14, 1050 Brussels, Belgium.ORCID 0000-0001-9218-078X

Funding

Belgian Federal Public Service of Health, Food Chain Safety and Environment GENEDIT RF 20/6342
6 · The paper itself

Abstract

Similar to genetically modified organisms (GMOs) produced by classical genetic engineering, gene-edited (GE) organisms and their derived food/feed products commercialized on the European Union market fall within the scope of European Union Directive 2001/18/EC. Consequently, their control in the food/feed chain by GMO enforcement laboratories is required by the competent authorities to guarantee food/feed safety and traceability (2003/1829/EC; 2003/1830/EC). However, their detection is potentially challenging at both the analytical and interpretation levels since this requires methodological approaches that can target and detect a specific single nucleotide variation (SNV) introduced into a GE organism. In this study, we propose a targeted high-throughput sequencing approach, including (i) a prior PCR-based enrichment step to amplify regions of interest, (ii) a sequencing step, and (iii) a data analysis methodology to identify SNVs of interest. To investigate if the performance of this targeted high-throughput sequencing approach is compatible with the performance criteria used in the GMO detection field, several samples containing different percentages of a GE rice line carrying a single adenosine insertion in

Indexed as

CRISPR/Cas9detectionfood and feed chaingenetically modified organismhigh-throughput sequencingPCR-based enrichmentsingle nucleotide variationstransgenic rice

Identifiers

PMID36765984
PMCPMC9914749

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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.