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Science in the Open

The online home of Cameron Neylon
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When I saw the anonymous piece “Openness is Inclusivity” it both struck a chord and made me uncomfortable. Striking a chord because I’m increasingly concerned about the institutionalization and centralization of Open Science activities. Uncomfortable because it comes across as an attack, and an anonymous one at that, on one organization.

Published

It has been painful to watch the tensions at the Wikimedia Foundation explode over the last few months and with the stepping down of the Executive Director there seems a mood of conciliation and a desire for WMF to learn from the process. I know next to nothing of the details or the story, so while it is the spur for this post I don’t want to offer any opinions on WMF itself.

Published
Author Geoffrey Bilder

Cite as “ Bilder G, Lin J, Neylon C (2016) Where are the pipes? Building Foundational Infrastructures for Future Services, retrieved [date], https://cameronneylon.net/blog/where-are-the-pipes-building-foundational-infrastructures-for-future-services/ ‎” You probably don’t think too much about where all the services to your residence run. They go missing from view until something goes wrong.

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I’m not much for end of year or beginning of year posts but I have found that putting down plans is a good way of holding myself to account (and that a few people out there might help with that job…you know who you are). I also think my use of this space may change a little over the coming year, so for those of you still using RSS (yes! we do still exist!) this may have an impact on including me or not in your selection for 2016.

Published

I’ve been engaged in different ways with some people in the rare genetic disease community for a few years. In most cases the initial issue that brought us together was access to literature and in some cases that lead towards Open Science issues more generally. Many people in the Open Access space have been motivated by personal stories and losses, and quite a few of those relate to rare genetic diseases.