Congenica Ltd and the UK Northern Health Science Alliance announced today a strategic partnership to deliver more accurate diagnostic tools and improve outcomes for patients with genetic conditions which involves teaming up with University of Manchester experts.
The aim of the partnership is to accelerate the development of collaborations between Congenica Ltd, a clinical genome diagnostics and discovery company, and that of the leading universities and NHS hospital Trusts in the North of England.
The first proof-of-principle agreement under the partnership has already been formed between Congenica Ltd and Central Manchester University Hospitals NHS Foundation Trust.
The overarching partnership will bring together clinical genetic expertise, molecular diagnostic testing and large-scale genome analytics to develop and implement the next generation sequencing based analysis pipelines, genome-wide interpretation and reporting tools for diagnostic testing.
This unique system will be rolled out to a variety of different applications and available through service and licensing business models. Congenica’s genome analytics platform, which is scalable and capable of processing many thousands of samples per year, is central to the partners’ ambitious plans. Congenica’s genome analytics platform uses state-of-the-art statistical and computational methods, and has the flexibility to evolve with the rapidly changing next generation sequencing technology and clinical applications.
Under the agreement between Congenica and Central Manchester University Hospitals NHS Foundation Trust, the partners will create a reference laboratory. Based at the Manchester Centre for Genomic Medicine, the reference laboratory will undertake genome screening of patients and their unaffected relatives in order to generate a comprehensive genetic profile and clinical report to support diagnosis, the clinical decision making, treatment choice, and counselling.
The partnership will concentrate efforts on developmental disorders, which account for approximately 30% of all genetic disease, but will then follow-on with programs in other therapeutic indications such as ophthalmological, cardiovascular and neurological disease.
“In 2001 the world witnessed the sequencing of the human genome, now in 2014 we are developing tools to help clinicians embed genomic medicine in the clinic. The partnership between Congenica and the Northern Health Science Alliance will further help us understand the utility of genomic medicine and bring the technology one step closer to routine clinical practice”, said Dr Hakim Yadi, Chief Executive of the Northern Health Science Alliance.
“Congenica is extremely pleased to enter into partnership with the NHSA and Central Manchester University Hospitals NHS Foundation Trust. The age of precision medicine is upon us and this is a great opportunity to bring together the wealth of clinical expertise and innovation at Manchester with our scalable genome analytics and clinical decision support tools”, said Dr Tom Weaver, CEO of Congenica. “We strongly believe that partnering is the best way to facilitate rapid adoption of our technology and make a real impact on tackling genetic disease in the clinic.” Manchester Academic Health Science Centre partners, Central Manchester University Hospitals NHS Foundation Trust andThe University of Manchester are renowned for their world-leading clinical and research expertise in genomic medicine.
Together, they are founders of the Manchester Centre for Genomic Medicine (MCGM), an integrated academic and service department based at Central Manchester University Hospitals NHS Foundation Trust.
Professor Graeme Black, Professor of Genetics at The University of Manchester and Strategic Director at the Manchester Centre for Genomic Medicine and Consultant in Genetics and Ophthalmology, said: “Manchester was an early adopter of Next Generation Sequencing, and we provide clinical and diagnostic services for inherited disorders to a population of over six million individuals. We bring a wealth of diagnostic and clinical expertise in the diagnosis and management of rare diseases.”
Notes for editors
For further information, please contact: Dr. Thomas Weaver, CEO, Congenica Ltd, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK. T: +44 (0) 778-066-0911; E: firstname.lastname@example.org Karl Milner, Director of Communications, Northern Health Science Alliance, karl.milner@theNHSA.co.uk. Emma Smith, Marketing Manager, Central Manchester University Hospitals NHS Foundation Trust. T: +44(0)161-701-2679 / (0)782-514-2219; E: email@example.com.
About Congenica Ltd Congenica is a UK start-up company founded on pioneering research from the Wellcome Trust Sanger Institute, NHS clinicians and genetic testing laboratories. We are translating this research into a gold standard clinical genomic analytics platform, SAPIENTIATM, for processing big data sets of human DNA sequence with deep clinical phenotype information in order to generate a definitive molecular diagnosis and clinically actionable interpretation of genetic disease for treatment, patient stratification and drug discovery. Our service and discovery efforts are provided to medical practitioners and drug developers for diagnostic, prognostic and clinical research purposes. For more information on the Company, please visit our website at www.congenica.com.
About the Northern Health Science Alliance The Northern Health Science Alliance Ltd (NHSA) is a new partnership established by the leading Universities and NHS Hospital Trusts in the North of England to improve the health and wealth of the region by creating an internationally recognised life science and healthcare system. The company acts as focal point for NHSA members, including the four Academic Health Science Networks in the North of England and partner organisations to work collaboratively on projects that leverage the combined potential of the North.
The NHSA supports its partners in working together to harness the resources, infrastructure, intellectual capital and experience of the whole Northern healthcare ecosystem. Further information is available at: www.theNHSA.co.uk. About the Manchester Centre for Genomic Medicine The Manchester Centre for Genomic Medicine is a partnership between the CMFT and IHD and represents one of the most comprehensive units in Europe. An integrated academic and service department based at CMFT, it provides clinical and diagnostic services for inherited disorders to a population of over six million individuals and leads an international programme of research. (http://www.mangen.co.uk).