The Resource Identification Initiative: A cultural shift in publishing

A central tenet in support of research reproducibility is the ability to uniquely identify research resources, i.e., reagents, tools, and materials that are used to perform experiments. However, current reporting practices for research resources are insufficient to allow humans and algorithms to identify the exact resources that are reported or answer basic questions such as "What other studies used resource X?" To address this issue, the Resource Identification Initiative was launched as a pilot project to improve the reporting standards for research resources in the methods sections of papers and thereby improve identifiability and reproducibility. The pilot engaged over 25 biomedical journal editors from most major publishers, as well as scientists and funding officials. Authors were asked to include Research Resource Identifiers (RRIDs) in their manuscripts prior to publication for three resource types: antibodies, model organisms, and tools (including software and databases). RRIDs represent accession numbers assigned by an authoritative database, e.g., the model organism databases, for each type of resource. To make it easier for authors to obtain RRIDs, resources were aggregated from the appropriate databases and their RRIDs made available in a central web portal ( www.scicrunch.org/resources). RRIDs meet three key criteria: they are machine readable, free to generate and access, and are consistent across publishers and journals. The pilot was launched in February of 2014 and over 300 papers have appeared that report RRIDs. The number of journals participating has expanded from the original 25 to more than 40. Here, we present an overview of the pilot project and its outcomes to date. We show that authors are generally accurate in performing the task of identifying resources and supportive of the goals of the project. We also show that identifiability of the resources pre- and post-pilot showed a dramatic improvement for all three resource types, suggesting that the project has had a significant impact on reproducibility relating to research resources.

[1]  Hans-Michael Müller,et al.  The Neuroscience Information Framework: A Data and Knowledge Environment for Neuroscience , 2008, Neuroinformatics.

[2]  Priyanka Rathore,et al.  Cautionary notes on the use of NF-κB p65 and p50 antibodies for CNS studies , 2011, Journal of Neuroinflammation.

[3]  R. Fluck,et al.  Treatment needs and diagnosis awareness in primary care patients with chronic kidney disease. , 2012, The British journal of general practice : the journal of the Royal College of General Practitioners.

[4]  Ron Mengelers,et al.  The Effects of FreeSurfer Version, Workstation Type, and Macintosh Operating System Version on Anatomical Volume and Cortical Thickness Measurements , 2012, PloS one.

[5]  Maryann E. Martone,et al.  A Comparative Antibody Analysis of Pannexin1 Expression in Four Rat Brain Regions Reveals Varying Subcellular Localizations , 2012, Front. Pharmacol..

[6]  Brian A. Nosek,et al.  Power failure: why small sample size undermines the reliability of neuroscience , 2013, Nature Reviews Neuroscience.

[7]  Nicole A. Vasilevsky,et al.  On the reproducibility of science: unique identification of research resources in the biomedical literature , 2013, PeerJ.

[8]  M. Herkenham,et al.  Minimal NF-κB activity in neurons , 2013, Neuroscience.

[9]  Anita Bandrowski,et al.  Promoting research resource identification at JCN , 2014, The Journal of comparative neurology.

[10]  Amanda Capes-Davis,et al.  Cell line cross-contamination: WSU-CLL is a known derivative of REH and is unsuitable as a model for chronic lymphocytic leukaemia. , 2014, Leukemia research.

[11]  Perry L. Miller,et al.  Extending the NIF DISCO framework to automate complex workflow: coordinating the harvest and integration of data from diverse neuroscience information resources , 2014, Front. Neuroinform..

[12]  Christian Kaltschmidt,et al.  An Investigation of the Specificity of Research Antibodies against NF-κB-subunit p65 , 2014, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[13]  Jean-Michel Hupé,et al.  Statistical inferences under the Null hypothesis: common mistakes and pitfalls in neuroimaging studies , 2015, Front. Neurosci..

[14]  D. Daniels,et al.  Enhanced consumption of salient solutions following pedunculopontine tegmental lesions , 2015, Neuroscience.