See what you could detect before you commit a sample.
The published science, the disease-area reviews and the practical guides, each framed around what the data means for your trial, your laboratory and your patients. Start with what matters to your work, then go straight to the source.
Performance in numbers, from the work already done.
Publications
Peer-reviewed papers, each with a plain-language note on what the result means for you and a permanent link to the source.
Disease areas
Deep reviews by indication: paediatric solid tumours, and CNS tumours read in cerebrospinal fluid. The evidence, the data, and what each lets you do.
White papers
Practical guides from our scientific team, starting with how to design a ctDNA endpoint into an oncology trial.
Start with these three.
A review, a guide and a result. The full, filterable list lives on the Publications page.
CNS tumours: reading glioma in the cerebrospinal fluid.
What CSF ctDNA lets neuro-oncology teams do that plasma cannot, with the sensitivity data and the Epistamai Bio case behind it.
Paediatric solid tumours: detecting relapse before imaging can.
What ultra-sensitive ctDNA lets paediatric teams do that they currently cannot, with the sensitivity data and evidence behind it.
Circulating tumour DNA as a biomarker in clinical trials.
For pharma and CRO teams: MRD enrichment, response monitoring and ctDNA endpoints, and how they cut trial size and cost.
Can't find evidence for your indication?
Tell our scientific team what you are working on and we will point you to the most relevant data, including unpublished work we can share under agreement.
This hub brings the different kinds of evidence together: papers, disease-area reviews and white papers. Publications is the deeper, fully citable list of peer-reviewed work on its own.
Peer-reviewed papers are copyright of the publisher, so we link to the version of record via its DOI, which is permanent and authoritative. Where a paper is open access, we may also offer the PDF.
Our own white papers are hosted here. Some ask for a few details first so we can stay in touch.
Speak to our scientific team.
A real human, in CET/CEST time zone, who has run samples like yours.