OUR TECHNOLOGY

 

A barcoded duplex chemistry that separates real signal from background error.


For the visitor who already knows tumour-informed ctDNA monitoring and wants to see the underlying chemistry, the validated performance and the limits we are open about. No marketing layer.

 
HOW IT WORKS

 

Three things our technology does that conventional technology does not.

1

Single-molecule duplex barcodes

Each original cfDNA molecule gets a unique, double-stranded barcode before any amplification. That means every read can be traced back to the exact starting molecule and its complementary strand.

2

Consensus-based error suppression

Variants are called only when they appear consistently across multiple PCR copies and on both strands of the original molecule. Polymerase errors and sequencing artefacts are filtered out by design.

3

Tumour-informed personalised panels

The panel is built from the patient's own tumour profile, not a fixed gene list. That focuses sensitivity on the variants that matter for that specific tumour, and keeps the per-sample cost workable.

simsen-seq-how-it-works
VALIDATED PERFORMANCE

 

What the platform delivers, in numbers a scientist can use.

LIMIT OF DETECTION

<0.001 VAF

input requirement

10-50 ng cfDNA

sequencing platform

Illumina

Single-molecule resolution. Published in Nature Protocols. Validated on cfDNA panels across paediatric, surgical and translational cohorts. Low input by design. Works with small plasma volumes, paediatric samples and early-stage cohorts where most platforms run out of starting material.
Runs on all Illumina sequencers. LabSuite kits are validated on the platform most European laboratories already operate. No proprietary box to buy.

 

SAMPLE TO RESULT

 

Five steps from plasma to clinical report.


The same workflow whether you send samples to our lab or run SiMSen-Seq in-house on LabSuite. Click any step for what happens, what we need, and what you get back.

Sample collection and cfDNA isolation.

Sequencing on Illumina or Element platforms. The Simsen pipeline collapses reads into duplex consensus families, removes single-strand and discordant artefacts, and calls variants only where signal is consistent across the family. Raw BAM and FASTQ are delivered alongside the call set.

Run our pipeline, run yours, or run both. The data is open by design.
.

WHAT WE NEED

PLASMA

4-10 mL, stabilised collection tube

TUMOUR

FFPE block or fresh tissue, for panel design

TURNAROUND

Sample receipt within 5 working days

Personalised panel design from the patient's tumour.

Tumour exome or targeted sequencing identifies the patient-specific variants worth tracking. The panel typically covers 20-50 personalised SNV targets per patient, weighted toward clinically actionable variants and tumour markers that drift with treatment.

Panel design takes about two weeks; once the panel is built, subsequent plasma samples run on a standard turnaround.

What you get

Panel size

20–50 personalised targets

Design time

~2 weeks from tumour sample

Reusable

Same panel across all longitudinal plasma points

SiMSen-Seq library preparation.

Duplex molecular barcoding before any amplification. The library is built so every original cfDNA molecule has a unique, traceable tag, and both strands of the duplex are kept through the workflow. This is what makes the consensus error suppression in step 4 possible.

LabSuite ships the library prep kit and protocol so the same chemistry runs in your laboratory exactly as in ours.

KIT Contents

Format

LabSuite distributed kit or in-lab

Hands-on time

~4 hours per batch

Batch size

Up to 96 samples

Sequencing and consensus calling.

Sequencing on Illumina platforms. The Simsen pipeline collapses reads into duplex consensus families, removes single-strand and discordant artefacts, and calls variants only where signal is consistent across the family. Raw BAM and FASTQ are delivered alongside the call set.

Run our pipeline, run yours, or run both. The data is open by design

OUTPUT

RAW DATA

FASTQ + BAM, customer-owned

PIPELINE

Open, documented, reproducible

COVERAGE

10,000× consensus, typical

Clinical report and longitudinal view.

Report built for the people reading it: clinicians, study teams, principal investigators. Each variant is shown with VAF, clinical rationale and trajectory across longitudinal samples. Resistance markers and clonal evolution are surfaced where present.

Reports are available as PDF and can be returned via API into your clinical or trial database

DELIVERY

TURNAROUND

10-15 working days, standard plasma

FORMAT

PDF

LANGUAGES

English; per-trial localisation on request

TECHNOLOGY

SiMSen-Seq, the science under the hood.

Barcoded duplex sequencing, error suppression and the sample-to-result workflow, with performance data.

Read the technology page →

COMPARISON

SNV vs SV vs tumour-naive.

The three families of tumour-informed monitoring, side by side, and a four-question decision guide.

Compare the methodologies →

DELIVERY

Full-service lab or LabSuite kits.

The two delivery models, the trade-offs on cost, control, turnaround and capability.

See both delivery models →

FOUR WAYS IN

 

Where our technology is strong, and where it is not.


An honest read on the platform. Sensitivity below 0.001% VAF is real and validated. There are sample types and clinical questions where another approach is the right choice. We will tell you which.

Sensitivity scales with consensus depth.


The chart on the right shows expected detection confidence as a function of variant allele frequency, across three consensus depth tiers. At 10,000× consensus, the platform resolves single-molecule signal in the parts-per-million range.

For very high-burden cases, lower consensus depth is sufficient and faster. For minimal residual disease and paediatric work, depth is the right lever.

sensitivity-vs-consensus-depth

When SiMSen-Seq is not the right tool

If no tumour tissue exists, or sensitivity is secondary, a tumour-naive panel may serve you better.

Tumour-informed monitoring requires a tumour sample for panel design. If the case is post-mortem, pre-biopsy or otherwise tissue-absent, a fixed tumour-naive panel is the correct call. We will say so, and we maintain comparisons with the leading alternatives on the Methodology page rather than hiding them.

Peer-reviewed

 

Validated where it matters: in independent journals.

A selection of the foundational and applied publications. Filter the full list on the Evidence page.

FOUNDATIONAL CHEMISTRY

SiMSen-Seq: simple, multiplexed, sensitive sequencing for the detection of low-frequency variants.

Stahlberg A, et al. Nature Protocols, 2017

Read the publication →

COMPARISON

SNV vs SV vs tumour-naive.

The three families of tumour-informed monitoring, side by side, and a four-question decision guide.

Compare the methodologies →

FOUNDATIONAL CHEMISTRY

SiMSen-Seq: simple, multiplexed, sensitive sequencing for the detection of low-frequency variants.

Stahlberg A, et al. Nature Protocols, 2017

Read the publication →

COMPARISON

SNV vs SV vs tumour-naive.

The three families of tumour-informed monitoring, side by side, and a four-question decision guide.

Compare the methodologies →

TALK TO US
 

Speak to our scientific team.

A real human, in CET/CEST time zone, who has run samples like yours.