With a rapid turnaround time, we can provide results for negative samples within 24, enabling swift clinical decisions.
16S and/or 18S rRNA amplicon sequencing

16S and/or 18S rRNA amplicon sequencing
Our 16S and 18S rRNA amplicon sequencing service offers a fast and reliable method for identification of bacterial and fungal DNA in clinical samples.
The detection of bacterial and fungal pathogens through molecular methods, such as 16S and 18S rRNA amplicon sequencing, is critical for identifying infections where traditional culture methods may be slow or inconclusive. The 16S rRNA gene is highly conserved among bacteria, making it an ideal target for broad-range bacterial detection, while the 18S rRNA gene serves as a reliable marker for fungal identification. These techniques allow for the rapid identification of microbial DNA directly from clinical specimens.
This fully CE-IVD nucleic acid extraction and broad-range detection assay, combined with species-level identification through sequencing of positive samples, is crucial for diagnosing infections in cases where empirical treatment may be insufficient or where timely identification can significantly improve patient outcomes. This approach is particularly valuable in diagnosing infections in sterile sites or in cases of invasive disease where the causative agent is not easily culturable. For further information on the benefits of molecular diagnostics in infection management, refer to current clinical guidelines on molecular pathogen detection.
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Our Services




Bodily fluids, Tissue
Enfer Medical
Tests/Assays
16S and or 18S rRNA amplicon sequencing


Patient
Request Form
Results are reviewed by experienced clinical scientists to ensure accuracy and clinical relevance.
All reports are delivered electronically and can be securely accessed anytime via the Enfer Medical Portal, providing convenient and confidential access for clinicians.



Results are available within 24 – 72h.
Frequency of testing
Packaging
The packaging/preparation of samples for delivery to the laboratory are required to be in adherence to all national regulations for the safe transport of biological materials. HSE guidance can be reviewed HERE.
There are specific packaging instructions and labelling requirements requiring triple packaging including:
- Primary leak-proof container – tube or vial containing the sample.
- Secondary watertight container, with absorbent material, intended to protect the primary container.
- Outer container protects the secondary container.
- Patient Request forms must be placed between the secondary container and the outer shipping container.
Further information on the packaging/preparation of samples for delivery to the laboratory is contained within the Enfer Medical Laboratory User Manual which clients are provided with.


Storage & Stability
Specimens must be stored at 2-8°C and tested within 7 days of collection.


Samples
In addition to the packaging of samples, the transport/delivery of clinical samples to the laboratory is required to be in adherence to all national regulations for the safe transport of biological materials. Enfer Medical provides a fully compliant logistics service, aligned with clients’ testing requirements.
Prompt transport of specimens:
To ensure prompt testing of samples and release of results within the published test turnaround times, samples should arrive to the laboratory by 18:00. Test turnaround time is measured from receipt of the sample at the laboratory until the time the authorised results are reported to users.
of Samples
In rare cases specimens may not be suitable for testing on arrival to the laboratory. In that case the sample will be rejected at the receipt stage and the service user will be notified immediately and an explanation as to why the sample could not be processed will be provided. Reasons why samples cannot be processed include but are not limited to:
- Samples received beyond the stability limits and/or not at the correct temperature indicated for each test.
- Incorrect sample type received.
- Leaking samples, sample not received or sample insufficient for analysis as stated below within sample requirements.
- Non-compliant samples or request forms i.e. those missing sample date information, missing sample test request and/or missing sample site/type information.
- Samples received without the necessary patient identifiers.
Our Services




- [Bacterial species X detected], [Fungal species X detected]
Accessing
Your Results
Results are reviewed by experienced clinical scientists to ensure accuracy and clinical relevance.
All reports are delivered electronically and can be securely accessed anytime via the Enfer Medical Portal, providing convenient and confidential access for clinicians.

