(C) PLOS One This story was originally published by PLOS One and is unaltered. . . . . . . . . . . From policy to practice: Lessons learned from an open science funding initiative [1] ['Sonya B. Dumanis', 'Coalition For Aligning Science', 'Chevy Chase', 'Maryland', 'United States Of America', 'Aligning Science Across Parkinson S', 'Asap', 'Kristen Ratan', 'Strategies For Open Science', 'Stratos'] Date: 2024-02 Competing interests: I have read the journal’s policy and the authors of this manuscript have the following competing interests: SBD, HVS, ML, RS, and EAR are ASAP staff, KR was paid as a consultant for this work, THV and SM are part of DataSeer, the vendor we contracted with to support our compliance assessment. EAR & SBD serve as ASAP Executive Leadership, which makes funding decisions on research grants. Introduction In the past few years, there has been a notable shift in the open science landscape as more countries and international agencies release recommendations and implementation guidelines for open scholarship [1–7]. In August 2022, the US White House Office of Science and Technology (OSTP) released a memo [8] with guidance that all federally funded research articles be (1) open access and (2) include sharing of underlying datasets in public repositories. The global open scholarship conversation has shifted from making a case for open science to developing operational workflows to assess, monitor, and enforce open policies that can normalize, simplify, and streamline these processes for use in daily research practice. As various workflows are proposed, there is a need for collective action across funders, institutions, and governments to align on open science policies and practices to reduce the cost and friction of adoption [9–12]. Here, we examine the practices of the Aligning Science Across Parkinson’s (ASAP) initiative [13], whose mission is to accelerate the pace of discovery and inform the path to a cure for Parkinson’s disease through collaboration, research-enabling resources, and data sharing [14,15]. ASAP was conceived through an open-by-design framework from the start. To learn more, please see the ASAP Blueprint for Collaborative Open Science [16], which provides a detailed overview of the ASAP open science policies, templates, and reports. Grantees within the ASAP Collaborative Research Network (CRN), an international, multidisciplinary, and multi-institutional network of collaborating investigators, are already required to be compliant with the recommendations of the OSTP memo by adhering to ASAP’s open science policies [17]. For example, ASAP requires the posting of a preprint at the time of (or before) article submission, immediate open access for all publications, and a mandatory CC-BY license. Additionally, at the time of publication, all underlying research outputs (protocols, code, datasets) must be posted to a FAIR repository [18,19] and all research outputs from ASAP-funded research must have DOIs or other appropriate identifiers, such as RRIDs for material resources, appropriately linked to the manuscript (see Table 1 for list of identifier types). Here, we evaluate the feasibility, ease, impact, and improvement to our open science policies as they were implemented within the ASAP CRN program and discuss our lessons learned to assist other funders and institutions considering open science implementation. Tracking compliance for open science To assess ASAP’s effectiveness in upholding best open science practices for linking research outputs within an article and tracking compliance, ASAP partnered with an AI startup, DataSeer, which uses natural language processing and machine learning software to identify and assess the research outputs in a manuscript. The software simultaneously tallies the quantity, citations, and sharing status of newly generated and existing datasets, code, software, protocols, and lab materials. A DataSeer curator generates a report summarizing action items required for the article to meet compliance with ASAP policies. DataSeer receives articles through ASAP staff submissions and will return the resulting report assessment for ASAP staff to review and share with authors. Based on ASAP staff feedback, the authors may make amendments to update their manuscript. The submission, curation, and adjustment process are iterative, with the ASAP staff providing continual feedback to CRN teams until compliance is achieved. An example template of what the report looks like was deposited in Zenodo (https://doi.org/10.5281/zenodo.7504034). ASAP currently supports 35 different teams within the CRN. A CRN team is led by a core group of 3 to 5 lead investigators, and together with their respective labs and other optional collaborators, they work to complete the goals of their grant. Most of the research articles submitted to ASAP staff for compliance review from the CRN teams come from the team’s project manager (PM), a position allocated within the CRN team’s grant budget. At the start of the award, teams must identify an interim PM within their lab and then hire a permanent full-time PM within 3 months of the award. The PMs assist with ASAP open science policy compliance, facilitate collaboration across the network through identifying synergistic opportunities and resources for their teams to leverage, support onboarding of new team members that join their CRN team, and ensure that teams are completing their listed deliverables within their grant. In addition to utilizing the PMs, ASAP staff also received a list of articles through OA.Report (RRID: SCR 023288). OA.Report has a discovery process in which they scrape the web for any mention of Aligning Science Across Parkinson’s within an article’s acknowledgment sections. See Fig 1 for the workflow schematic. PPT PowerPoint slide PNG larger image TIFF original image Download: Fig 1. Schematic of the compliance workflow for ASAP grantees. Two main mechanisms discover ASAP-funded articles: either by team PMs or through OA.Report, and then submitted to the open science team on a rolling basis. OA.Report identifies papers by looking at the acknowledgment sections of preprints and publications for reference to Aligning Science Across Parkinson’s. Once received, DataSeer generates a compliance output report, which is checked by ASAP staff, and then shared with the article’s authors. Authors use the compliance report to understand what research outputs are not properly cited and recommendations for proper citation. After the article is revised, it is resubmitted to DataSeer and curated again. The assessment–curation–adjustment process can be repeated until all research outputs are appropriately cited. Finally, when the article is ready for publication, the report is assessed one final time for compliance. https://doi.org/10.1371/journal.pcbi.1011626.g001 Standardized research output compliance rules Our initial challenge in running the reports and conducting this analysis was around establishing clear rules on what was considered an accurately cited research output. Currently, no community-wide accepted standards exist across output types. Therefore, ASAP and DataSeer developed criteria based on FAIR standards [18,19]. FAIR rules are well-established for data and generally applicable for code scripts but have yet to be concretely applied to other trackable research outputs in academic publications. We decided to count any output as properly shared if an output had a specific, functioning, stable identifier(s) associated with it. Table 1 lists the definitions of ASAP’s tracked research output types (data, code and software, lab resources, protocols) associated with a manuscript. Table 2 displays the criteria for how these output types would be considered appropriately shared per ASAP guidelines. Our current workflow is a foundational starting point that allows for future changes to the definitions to be implemented at scale. PPT PowerPoint slide PNG larger image TIFF original image Download: Table 2. Identifier requirements for appropriately shared research outputs. This table highlights the different stable identifiers required for each specific output type to be counted as accurately cited in a manuscript. https://doi.org/10.1371/journal.pcbi.1011626.t002 Assessing impact: Compliance reports and measuring behavior change Compliance reports from DataSeer track and evaluate baseline compliance, before any intervention, as well as compliance after an article is versioned. In the manuscript lifecycle, there can be multiple versions of a manuscript from the draft manuscript to the preprint posted, to the version submitted for peer review, to the resulting manuscript version released for publication. For this analysis, we tracked how the versions, drafts throughout the manuscript lifecycle, changed over time. This helps us understand the change over time as a research team amends any issues that ASAP staff raised related to output sharing in an article following a compliance report. To understand user behavior, we assessed output sharing in the first and second versions of the manuscripts through the DataSeer workflow (Fig 1). Because we continually refined the research output rules through February 2022, we restricted evaluation to articles submitted to DataSeer after March 1, 2022 (termed the first version). The subsequent submission (termed the second version) were articles submitted to DataSeer at least 2 business days after the first version. This criterion was included as sometimes a draft manuscript was received the day it was uploaded to a preprint server, which appeared online 2 days later. Within this criterion, 19 articles had a first and second version submission through the DataSeer system between March 1, 2022 and October 1, 2022, and these were the articles analyzed in our assessment. We tallied the number of outputs identified and cited appropriately in the first and second version of the manuscripts based on ASAP’s standards (Table 2) for each newly generated and reused research output type (datasets, code and software, lab materials, and protocols). In Table 3, we report the numbers in 2 ways: the proportion of outputs shared across all outputs identified in all papers (the purple columns) and the average proportion of outputs shared per paper (green columns). Please see Table 3 and Fig 2 for a summary of the overall results by output type. PPT PowerPoint slide PNG larger image TIFF original image Download: Fig 2. Compliance review increases the sharing of new and reuse research outputs. We assessed compliance with ASAP’s open science policy at 2 stages within the lifetime of ASAP-funded research articles: the first version submitted to ASAP for initial review and the subsequent version following said review. Compliance was assessed by measuring the percentage of novel and reuse research outputs (datasets, code/software, lab materials, and protocols) shared or cited in both versions. There were a total of 19 article pairs examined for this analysis. If a paper did not contain an output type in either the version 1 or version 2 assessment, it was excluded from the analysis for that output type. See Table 3 for the total number of papers included in each output assessment type. Within each panel, the y-axis represents the percentage of shared research outputs and the x-axis represents the 2 stages of manuscript development. Blue dots and green triangles represent unique manuscripts in the first and second versions. The first and second versions of research articles are connected via gray lines. (A) Percentage of new datasets shared across stages. (B) Percent reuse datasets cited across stages. (C) Percentage of new code software shared across stages. (D) Percentage of reuse code and software cited. (E) Percentage of new lab materials shared across stages. (F) Percentage of reuse lab materials cited across stages. (G) Percentage of new protocols shared across stages. (H) Percentage of reuse protocols cited across stages. https://doi.org/10.1371/journal.pcbi.1011626.g002 PPT PowerPoint slide PNG larger image TIFF original image Download: Table 3. Summary statistics for assessing compliance over time. Here, we report the summary statistics around the proportion of outputs shared across all outputs identified from papers in version 1 of the manuscript, before our review, and version 2 of the manuscript, after we highlighted the changes that needed to be made in the manuscript to accurately cite all research outputs. https://doi.org/10.1371/journal.pcbi.1011626.t003 As expected, all output types show an improvement in their sharing status in the second version of the manuscript after receiving a compliance report summarizing action items authors needed to take for each output type to achieve compliance per ASAP policies (Fig 2 and Table 3). In our follow up discussions with authors, we began to catalog the unique challenges by output type that prevented authors from achieving 100% compliance even after our outreach to authors. Below is a discussion of these specific barriers. Datasets On average, sharing of newly generated datasets increased from 12% in the first version to 69% in the second version (Fig 2A and Table 3). When asked why all datasets were not shared for a specific manuscript, the most common response was that the ASAP grantee had not generated the dataset in question, and the grantee could not control the actions of collaborators who were not funded by ASAP. Rarely is a funder the sole funder of a research publication, and ASAP began to draft guidelines for approaching new research collaborations and discussing ASAP policies. Code and software For the purposes of this discussion, we will use the term software liberally to apply to both code and software outputs. When assessing software sharing in the second version of manuscripts, there was a strong upward trend toward more software shared. Proper software linkages jumped from 6% in the first version to 65% in the second version of manuscripts for newly generated outputs. For software citing preexisting software (reused software citations), the numbers increased from 10% in the first version to 58% on average in the second version (Fig 2C and 2D). There were 2 factors often cited for noncompliance with properly citing software. First, there is a lack of consensus and education on how to cite software. There are 2 usual routes to citing software: a DOI generated by Zenodo, a general all-purpose open repository, or via a Research Resource Identifier (RRID). Most members of our network were unaware that Zenodo has capabilities to sync up with GitHub, a common web platform for writing code, to provide a digital object identifier (DOI) and make that code citable in a paper with an identifier. For those not using GitHub, they were unaware of what an RRID is, an identifier used to register lab materials and software, let alone where to register or find associated RRIDs for these materials using the SciCrunch database, which catalogs all registered RRIDs. For an overview of key resources that ASAP commonly uses, see Table 4. Adding to the confusion are the requests made by software developers to cite a specific publication describing the software versus an RRID or DOI number linking to software directly, which can generate confusion about which best practice to follow. Moreover, if the preexisting software being used has not already been registered with a permanent identifier in the SciCrunch database or other repositories such as Zenodo, there is also a hesitancy to register the software on someone else’s behalf. Moreover, doing so may also create multiple RRIDs for the same software instance. For example, we observed instances where the same software package may have multiple RRIDs associated with it, and it isn’t clear which RRID to select for citation purposes. PPT PowerPoint slide PNG larger image TIFF original image Download: Table 4. This table is a quick lookup table for all of the resources utilized in either generating the manuscript or referenced as an open science tool within the text. Key resources. https://doi.org/10.1371/journal.pcbi.1011626.t004 Lab resources The greatest challenge for authors was registering new lab materials generated from the manuscript. Even in the second version of manuscripts, only 6% of newly generated materials had an RRID associated with the output (Fig 2E). This is due to 2 main issues. First, getting a resource deposited and available for distribution in a registry takes time and money. Some of this can be allayed through preregistration mechanisms that assign an RRID to the material prior to it being publicly available. Certain resource types already have a preregistration workflow in place (e.g., a cell line can be preregistered with an RRID through Cellosaurus, a database of immortalized cell lines used in biomedical research), but there is a substantial knowledge gap within the researcher community about these workflows. Second, there needs to be more clarity on how an RRID should be registered, as different agencies govern different resource types with different procedures (e.g., antibodies are handled separately from cell lines which are handled separately from plasmids). Another source of confusion is in how to handle specific stable resources that currently do not have registering bodies that can mint RRIDs, such as newly generated gene probes or compounds generated for research purposes. There is no clear framework for using patent numbers or other isolated identifiers in such use cases. This results in a complex and fragmented landscape that is confusing for the average researcher to navigate and for the funder to provide clear guidelines. Protocols There was a strong upward trend toward sharing protocols (Fig 2G and 2H and Table 3). The percentage shared jumped from 13% in the first version to 53% in the second version on average. During our outreach, we learned that the most significant barrier to sharing methods was that authors were worried about plagiarism and didn’t understand why we required the methods sections to link to a recipe-style registered protocol. Most believed that the description in the methods section of a manuscript was enough information. To help teams, ASAP provided information on how protocols are not copyrighted material, emphasizing that credit should still be given, but anyone can upload a protocol (if it was not a trademarked secret) regardless of who generated it. Additionally, ASAP staff shared lessons learned from the Cancer Reproducibility Project, which was a great motivator in increasing adoption rate of sharing recipe-style protocols and registering with platforms like protocols.io [20]. Other considerations In our experience, even with PM support, the ones responsible for depositing the data are trainees with little to no formal education in their graduate school career about key considerations for curating datasets and other research outputs. To help train our network, ASAP recently developed a checklist for repository deposition [21], explaining the components to consider and the rationale for why it matters. In future, as open science policies evolve and become more widespread, educational training should become a required component of future research program curriculums. 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