About This Project
Drug-resistant tuberculosis (TB) is a race against time. Culture-based methods can take almost 8 weeks to reveal drug resistance. What if we could get answers sooner? ActiWGS TB asks: Can we recover enough DNA from blood spiked with Bacillus Calmette-Guérin (BCG), a safer TB model, for reliable whole-genome sequencing (reading bacterial DNA) without culture? We believe we can. We'll measure completeness and reliability, working toward 72-hour resistance results to ensure better patient outcomes.
Ask the Scientists
Join The DiscussionWhat is the context of this research?
TB doesn't wait, but testing often does. In 2024, 10.7 million people developed tuberculosis (TB) worldwide, according to WHO. Growing TB bacteria to see which medicines will work can take weeks, delaying care. Reading the TB genome (its full DNA instructions) could give answers sooner, but blood often contains too little bacterial DNA.
Here's the missing link: researchers have shown that bacteriophages, viruses that target bacteria, can help release bacterial DNA from blood. Others have read TB genomes from sputum (mucus coughed up from the lungs) without growing bacteria. Could we read a TB genome from blood?
We expect to recover enough DNA to read the genome reliably without growing bacteria. ActiWGS TB will test prepared blood containing Bacillus Calmette-Guérin (BCG), a safer TB model, and check how complete and consistent the results are. This is a first step toward detecting drug resistance within 72 hours, pending testing in patients.
What is the significance of this project?
What if we could read TB’s genetic blueprint without waiting weeks to grow the bacteria? Before that becomes possible, we must answer a crucial question: can phage-based extraction recover enough DNA for reliable whole-genome sequencing?
Recent research highlights DNA preparation as a major challenge. ActiWGS TB will test this approach using laboratory-prepared blood containing BCG, a safe TB model.
We will measure genome completeness, sequencing quality and reproducibility, identifying where the approach succeeds or not.
Why does this matter? Our findings will determine whether this technology is ready for further development and patient-sample studies, or needs improvement first. Even negative results will reveal important limitations.
Our ultimate goal: A TB drug-resistance profile directly from blood within 72 hours, without relying on expensive, centralised laboratories. Faster answers, earlier treatment decisions, and better patient outcomes, even in resource-limited settings.
What are the goals of the project?
ActiWGS TB will assess whether DNA recovered through a phage-based extraction approach can support whole-genome sequencing. Our initial study will use an attenuated BCG research model rather than patient samples, with specialist work provided through separately arranged partner-laboratory support. The crowdfunding budget will purchase 50 extraction kits, two sequencing library-preparation kits, two flow cells and essential consumables. We will assess whether the resulting data can be assigned to the expected genome, examine how much of that genome is represented, and document the quality and consistency of the results. Appropriate controls and repeat assessments will help us interpret the evidence. We aim to complete this first stage within three months of receiving funding, subject to procurement and laboratory access. Our deliverable is a concise feasibility report describing the results, limitations and priorities for further work; clinical validation will require separate funding.
Budget
ActiWGS TB seeks $4,995 for a three-month proof of concept. Can phage-extracted DNA from laboratory-prepared blood containing BCG support whole-genome sequencing?
Library preparation: 2 Oxford Nanopore V14 kits (SQK-LSK114), 6 preparations each, at $830 = $1,660.
Sequencing: 2 MinION R10.4.1 flow cells (FLO-MIN114) at $970 = $1,940.
DNA extraction: 50 phage-based tests at $17.50 = $875, including controls and repeat assessments.
Consumables and shipping: $520, comprising filtered tips ($100), low-binding tubes ($60), PCR tubes ($30), media/buffers ($80), supporting reagents and quality controls ($90), other disposables ($35), and shipping/handling ($125).
These supplies will help assess genome completeness, sequencing quality and reproducibility, informing whether further development is justified. Prices are estimates; laboratory services and sequencing hardware are not included.
Endorsed by
Project Timeline
Within three months of receiving funding, we will evaluate ActiWGS TB in four stages: demonstrate that phage-extracted BCG DNA passes through the sequencing and analysis pipeline; determine a preliminary single-sample detection limit; test barcoded multiplex sequencing; and estimate the detection limit when samples are pooled. We will share a brief update and results summary after each stage. Multiplex stages depend on access to suitable barcoding reagents and partner-laboratory support.
Nov 08, 2026
Project Launched
Feb 28, 2027
Successful sequencing of phage-extracted BCG DNA through the ActiWGS TB pipeline
Mar 15, 2027
Determine the preliminary limit of detection (LoD) for BCG DNA sequencing
Mar 31, 2027
Demonstrate multiplex sequencing of phage-extracted BCG DNA
Apr 30, 2027
Determine the preliminary limit of detection under multiplex sequencing conditions
Meet the Team
Eduard Roos
Ever since studying biology, and tuberculosis (TB) in particular, I have been fascinated by one question: How can we make healthcare more accessible to everyone, regardless of where they live or the resources available to them?
I hold a PhD in Molecular Biology from Stellenbosch University and have extensive research experience in tuberculosis diagnostics, molecular biology, and genomics. My career has included research positions at the Pirbright Institute and South Africa's Agricultural Research Council, as well as lecturing in Wildlife Health and Immunology at the Royal Veterinary College in the UK.
My published research demonstrates my experience in the scientific approaches underpinning ActiWGS TB, including:
Whole-genome sequencing of Mycobacterium bovis (2023), demonstrating how genomic analysis improves our understanding of TB transmission between wildlife populations.
Development of a molecular diagnostic assay for bovine TB (2019), investigating new ways to detect tuberculosis infection in wildlife.
My passion lies in bridging the gap between scientific discovery and practical solutions. I believe some of the most meaningful breakthroughs come from rethinking how we use technologies that already exist.
This thinking inspired ActiWGS TB. Drawing on my experience in TB research and whole-genome sequencing, I am leading this project alongside specialist laboratory collaborators to investigate whether we can obtain meaningful genomic information without the lengthy bacterial culture process.
For me, science is most rewarding when it moves beyond the laboratory and makes a real difference in people's lives.
Explore my research and scientific background
Additional Information
Project Backers
- 2Backers
- 1%Funded
- $40Total Donations
- $20.00Average Donation



