What does FAIR mean for agricultural science?

Andrew Lyons, a researcher at the Division of Agriculture and Natural Resources (ANR) of the University of California, wrote a blogpost about the FAIR principles, the GO FAIR initiative and what it means for agricultural research. “ANR academics are impacted by the data tsunami in at least two ways (neither for good). Like all practicing scientists, we have to deal with the… Continue reading

NIH awards to test ways to store, access, share, and compute on biomedical data in the cloud

Twelve awards totaling $9 million in Fiscal Year 2017 will launch a National Institutes of Health Data Commons Pilot Phase. A data commons is a shared virtual space where scientists can work with the digital objects of biomedical research, such as data and analytical tools. The NIH Data Commons will be implemented in a four-year pilot phase to explore the… Continue reading

European Open Science Cloud Declaration online

On 26 October 2017, the European Commission made the EOSC Declaration available to all scientific stakeholders, for their endorsement and commitments to the realisation of the EOSC by 2020. The Declaration emerged from the EOSC Summit of 12 June, where more than 80 key scientific stakeholders showed a strong sense of commitment, dedication and intellectual rigour with respect to the implementation of the… Continue reading

Science goes FAIR at Health-RI 2017

What does FAIR Data mean in practice? How can you make your data FAIR? What novel science becomes possible when research data become more FAIR? Luiz Bonino and Michel Dumontier will answer these pressing questions at the Health-RI conference on 8 December 2017 in Utrecht. Register for Health-RI 2017. View the conference programme. FAIR Data is rapidly becoming the new standard… Continue reading

Reuse of clinical data for research: overcoming the hurdles

The systems of the eight Dutch UMCs contain a wealth of patient data, such as medical images, physical examination results, and treatment outcomes. “These data have been collected to diagnose and treat patients, but we can reuse them to answer important research questions. However, reusing clinical data is not as simple as you may think. In addition to concerns about… Continue reading

The first Data4lifesciences symposium: a report

On 11 September 2017, the Centraal Museum in Utrecht hosted the very first Data4lifesciences symposium. D4LS Programme Manager Dr Jan-Willem Boiten: “This symposium was an important milestone for the programme; we presented an overview of our first results.” The NFU programme Data4lifesciences (D4LS) aims to realise an integrated research data infrastructure for biomedical research at the Dutch UMCs. DTL is actively involved… Continue reading

Watch the ELIXIR Webinar on the rare disease interoperability pilot

On 18 October 2017, Marco Roos presented an ELIXIR webinar ‘Rare Disease test case for ELIXIR interoperability backbone’. “The ELIXIR rare disease pilot aims to make data machine readable and linkable, making it easier for researchers to combine data from multiple sources,” explains Roos in the webinar. You can watch the webinar here.

Maastricht University’s Institute of Data Science lands two major research projects on FAIR data

The Institute of Data Science (IDS) at Maastricht University is the only European research group invited to take part in an international research project led by the National Center for Advancing Translational Sciences (NCATS) in the USA. “This will allow us to collaborate with the world leaders in translational research”, says Michel Dumontier, distinguished university professor of Data Science and… Continue reading

FAIR: Putting machine readability first

Barend Mons recently gave an interview about the FAIR principles and the GO FAIR initiative in the journal e-Data & Research. “The way science currently deals with the huge amounts of research data has to change. If you receive tax money for your research, you should take care of the data that you produce and facilitate reuse by others. The FAIR… Continue reading

Rare disease Summer School & BYOD: a report

In September 2017, the ELIXIR Rare Disease Use Case organised an International Summer School on Rare Disease and Orphan Drug Registries and a Bring Your Own Data workshop. The two events were organised and hosted by the National Centre for Rare Diseases – Istituto Superiore di Sanità in Rome. The organisation was supported by several organisations, including DTL and ELIXIR-NL. Read… Continue reading