Using a bespoke Next-Generation Sequencing (NGS) pipeline, we deliver deeper reads and faster insights for researchers and clinicians who cannot afford to wait.
Diagnostic pillars
Bespoke analysis for the most demanding clinical and research profiles.
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Mean depth (targeted)
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Structural resolution
Research frontiers
Our team moves beyond broad-spectrum analysis. We dive deep into the specific anomalies that define complex metabolic profiles.
The boutique
model
In a sea of automated "black box" laboratories, we offer a return to the collaborative science model.
For a high-stakes field like genetics, the value lies in the removal of administrative layers that often separate the clinician from the raw science.
Rapid iteration
If a specific case requires an adjustment, such as increasing the depth of coverage for a specific exon or altering the bioinformatics filter for a rare metabolic pathway, we can re-configure the pipeline within a 24-hour cycle.
Rapid iteration isn't just about speed; it's about the ability to perform "N-of-1" science, where the protocol is adapted to the patient’s unique phenotypic requirements rather than the other way around.
Data sovereignty
We believe that unfiltered data is the foundation of future discovery.
Our lab provides a full suite of computational outputs. This allows your team to perform independent secondary analysis or upload files to institutional repositories.
We don’t retain secondary use rights for your data for internal research or commercial sale. Once the analysis is complete, the digital assets are transferred to your secure portal, and our local copies are purged according to your specific security protocol.
Direct-to-scientist communication
This allows for immediate, nuanced discussions regarding mosaicism, borderline variants, or complex structural rearrangements.
If a researcher is developing a new assay, they can speak directly with our lab's wet-bench scientists to optimize sample prep or library construction before the first tube is even opened.
