DNAdigest interviews Aridhia
As promised last week in the DNAdigest’s newsletter, we are giving life to our first blog post interview. Be introduced to Mr Rodrigo Barnes, part of the Aridia team. He kindly agreed to answer our questions about Aridhia and their views on genomic data sharing.
Mr Rodrigo Barnes, CTO of Aridhia
1. You are a part of the Aridhia team. Please, tell us what the goals and the interests of the company are?
Aridhia started with the objective of using health informatics and analytics to improve efficiency and service delivery for healthcare providers, support the management of chronic disease and personalised medicine, and ultimately improve patient outcomes.
Good outcomes had already started to emerge in diabetes and other chronic diseases, through some of the work undertaken by the NHS in Scotland and led by one of our founders, Professor Andrew Morris. This included providing clinicians and patients with access to up-to-date, rich information from different parts of the health system.
Aridhia has since developed new products and services to solve informatics challenges in the clinical and operational aspects of health. As a commercial organisation, we have worked on these opportunities in collaboration with healthcare providers, universities, innovation centres and other industry partners, to ensure that the end products are fit for purpose, and the benefits can be shared between our diverse stakeholders. We have always set high standards for ourselves, not just technically, but particularly when it comes to respecting people’s privacy and doing business with integrity.
2. What is your role in the organisation and how does your work support the mission of the company?
Although my background is in mathematics, I’ve worked as a programmer in software start-ups for the majority of my career. Since joining Aridhia as one of its first employees, I have designed and developed software for clinical data, often working closely with NHS staff and university researchers. This has been great opportunity to work on (ethically) good problems and participate in multidisciplinary projects with some very smart, committed and hard-working people.
In the last year, I took on the CTO (Chief Technology Officer) role, which means I have to take a more strategic perspective on the business of health informatics. But I still work directly with customers and enjoy helping them develop new products.
3. What makes Aridhia unique?
We put collaboration at the very heart of everything we do. We work really hard to understand the different perspectives and motivations people bring to a project, and acknowledge expertise in others, but we’re also happy to assert our own contribution. We have also been lucky to have investors who recognise the challenges in this market and support our vision for addressing them.
4. Aridhia have recently won a competition for helping businesses develop new technology to map and analyse genes and more specifically to support the efforts of NHS to map whole genomes of patients with rare diseases or cancer. On which phase are you now and have you developed an idea (or even a prototype) that you can tell us more about?
It’s a little early to say too much about our product plans, but we have identified a number of aspects within genomic medicine that we feel need to be addressed. Based on our extensive experience in the health field, we think a one size fits all approach won’t work when it comes to annotating genomes and delivering that information usefully into the NHS (and similar healthcare settings). There will be different user needs, of course, but there are also IT procurement and deployment challenges to tackle before any smart solution can become common practice in the NHS.
We strongly believe that there is a new generation of annotation products and services waiting to emerge from academic/health collaborations. We believe that clinical groups have the depth of knowledge and the databases of cases that are needed to provide real insight into complex diseases with genetic factors, and we are keen to help these SMEs and spin outs validate their technology and get them ‘to market’ in the NHS and healthcare settings around the world.
Overall our initial objective is to help take world class annotations out of research labs and into operational use in the NHS. Both of these goals are very much in line with Genomic England‘s mandate to improve health and wealth in the UK.
5. Aridhia is a part of The Kuwait Scotland eHealth Innovation Network (KSeHIN). Can you tell us something more about this project and what your plans for further development are?
Kuwait has one of the highest rates of obesity and diabetes in the world, and the Kuwait Ministry of Health has responsibility for tackling this important issue. We’ve worked with the Dasman Diabetes Centre in Kuwait and the University of Dundee to bring informatics, education and resources to improve diabetes care. The challenge from the initial phase is to scale up to a national system. We think there are good opportunities to work with the Ministry of Health in Kuwait to achieve their goals as well as working with the Dasman’s own genomics and research programmes. This project is an excellent example of the combination of skills and resources needed to make an impact on the burden of chronic disease.
This is a sensitive subject of course, and we have to acknowledge that this is data that can’t readily be anonymised. Sharing, if it’s permissible, won’t follow the patterns we are used to with other types of data. That’s why we took an interest in the work DNA Digest is doing.
Earlier in the year, Aridhia launched its collaborative data science platform, AnalytiXagility which takes a tiered approach to the managed sharing of sensitive data. We make sure that we offer data owners and controllers what they need to ensure they feel comfortable in sharing data. AnalytiXagility delivers a protocol for negotiation and sharing, backed by a ‘life-cycle’ or ‘lease’ approach to the sharing and audit systems to verify compliance. This has been primarily used for clinical, imaging and genomics data to date.
In a ‘Research Safe Haven’ model, the analysts come to the data, and have access to that for the intended purpose and duration of their project. This system is in place at the Stratified Medicine Scotland – Innovation Centre, which already supports projects using genomic and clinical data. The model we are developing for genomic data extends that paradigm of bringing computing to the data. We are taking this step by step and working with partners and customers to strengthen the system.
From a research perspective, the challenges are likely to be related to having enough linked clinical data, but also having enough samples and controls to get a meaningful result. So we think we will see standards emerging for federated models – research groups will try to apply their analysis against raw genomic data at multiple centres using something like the Global Alliance 4 Genomics and Health API, and then collate results for analysis under a research safe haven model. We recently joined the Global Alliance and will bring our experience of working with electronic patient records and clinical informatics to the table.
Trust and transparency are important factors. I am interested in seeing what could be done to establish protocols and accreditations that would give participants visibility of how data is being used and how the benefits are shared.
Are you part of a project that facilitates data sharing for genomics research? Would you like to be featured on our blog? We would love to hear from you. Drop us an email or use our contact page to get in touch.