Our drug discovery science
Our expertise in therapeutic innovation includes target identification, validation & disease positioning; hit discovery; hit-to-candidate optimisation...
Access cutting-edge CRISPR technology to create and improve world-leading cancer medicines.
We deliver pooled CRISPR screens, in collaboration with leading researchers, that identify and validate new drug targets and approaches that will change the cancer landscape.
Our state-of-the-art institute leverages the combined global strengths of Cancer Research UK’s world-class scientific network and AstraZeneca’s oncology drug discovery and development experience to drive scientific innovation.
We identify innovative approaches to tackle traditionally hard-to-treat cancers by deepening our understanding of key drivers of cancer and resistance mechanisms.
The key to our success is researcher autonomy. We empower you to explore bold new ideas without restraint.
We work with AstraZeneca, sharing resources and expertise, but all Cancer Research Horizons projects are independent and resulting data will remain unencumbered.
Our team of CRISPR experts have the skills and technology to make your project a success.
We can run pooled CRISPR screens, supporting everything from initial assay design, Cas9 cell line generation, to bioinformatic analysis and interpretation of the screen data results.
We use an optimised CRISPR platform for pooled CRISPR knockout and activation screening that enables the identification of genome-wide genetic vulnerabilities. Our specialist CRISPR screen areas:
Our cutting-edge research tools include:
Our active technology development programme evaluates new CRISPR technologies, enabling us to perform more complex CRISPR screens and identify disease-relevance drug targets. Our development areas include:
If your research could benefit from access to novel, state-of-the-art CRISPR technology, we would love to work with you to progress your research. Our expert team can help you plan your project to give you the best opportunity for success.
As an indication, cost for projects entering the FGC starts at £4,000 per genome wide CRISPR knock-out screen in a established cancer cell line with standard characteristics (i.e. normal growth rates, media and serum requirements. Exact costs will vary depending on the complexity of the experimental setup). This cost will include:
Proposals are reviewed quarterly. Please get in touch with us to find out when the next deadline is.
To access the Functional Genomics Centre's screening capabilities you should be one of:
If you are unsure of your eligibility, please contact us at [email protected]
Please get in touch with Beatrice Lana to discuss your project ideas and submit your application. Read our proposal guidelines to find out more.
Cancer Research Horizons Triage Panel have the responsibility of prioritising projects to bring into the FGC on behalf of Cancer Research Horizons. Projects will be prioritised based on Cancer Research Horizons strategic priority, feasibility and deliverability.
Current member of Cancer Research Horizons Triage Panel are:
Doug Ross Thriepland
Director of the Functional Genomics Centre
As the Director of the Functional Genomics Centre, I work in close partnership with David to manage the centre of 22 scientists focused on using CRISPR gene editing for target discovery in cancer. I have been in early pharmaceutical R&D over a decade with eight of those years at AstraZeneca working on target discovery platforms. I have a PhD in virology from the University of Leeds and I am passionate about bringing new medicines to patients in different disease areas. My current focus at the FGC is on using CRISPR to help understand the biology of cancer and discover new drug targets.
David Walter
Group Leader at Cancer Research Horizons, CRUK lead of the FGC
I am a Group Leader at Cancer Research Horizons and the CRUK lead of the FGC, having worked here with Doug since the centre opened its doors three years ago. I have nine years of experience in functional genomics and pre-clinical oncology R&D. I gained my PhD in cell biology from the University of Basel, Switzerland and completed my post-doctoral studies at the University of Copenhagen in Denmark, where I studied the role of cell cycle regulators in genome maintenance.
Working with the FGC was very straightforward. We appreciated the clear, high-quality communication, enabling us to always know what stage the project was at and to discuss findings on completion.