Reward the forgotten foot soldiers of science
The story of CRISPR–Cas9 gene editing has tended to focus on a few key players.
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The story of CRISPR–Cas9 gene editing has tended to focus on a few key players.
Crowdsourcing the analysis of complex and massive data has emerged as a framework to find robust methodologies. When the crowdsourcing is done in the form of collaborative scientific competitions, known as Challenges, the validation of the methods is inherently addressed.
The focus on impact of published research has created new opportunities for misconduct and fraudsters, says Mario Biagioli.
A postdoc job is good for your career, but don't get stuck in an academic cul-de-sac, says Søren-Peter Olesen.
Senior staff at Nature, Science and other journals want to end inappropriate use of the measure.
Late nights, typos, self-doubt and despair. Francis Collins, Sara Seager and Uta Frith dust off their theses, and reflect on what the PhD was like for them.
Doctoral courses are slowly being modernized. Now the thesis and viva need to catch up.
Thirty years on from the first congress on peer review, Drummond Rennie reflects on the improvements brought about by research into the process — and calls for more.
Users urge caution in revamp of service at the heart of physics.
Heads of research agencies from nearly 50 countries — large and small, with developed and emerging economies — adopted a Statement of Principles and Actions Promoting the Equality and Status of Women in Research at the Global Research Council's fifth annual meeting last month in New Delhi.
An analysis of Australian Research Council data reveals grant proposals that integrate a broad array of academic fields are less likely to be funded.
'Trap’ URLs can help publishers to catch automated downloading, but critics say that the approach is clumsy.
Problems of modern society demand collaborative research.
Marc Fleurbaey and colleagues explain why and how 300 scholars in the social sciences and humanities are collaborating to synthesize knowledge for policymakers.
Pooling clinical details helps doctors to diagnose rare diseases — but more sharing is needed.
The technique's first test in people could begin as early as the end of the year.
Staff at Canadian university given little guidance on how to mitigate future problems.