Tag Archives: policy

In conversation with Wellcome Trust and CRUK

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On Friday 22 January Cambridge University invited our two main charity funders to discuss their views on data management and sharing with Cambridge researchers. David Carr from the Wellcome Trust and Jamie Enoch from Cancer Research UK came to the University to talk to our researchers.

The related blog ‘Charities’ perspective on research data management and sharing‘ summarises the presentations Jamie and David gave. After this event, a group of researchers from the School of Biological Sciences and from the School of Clinical Medicine at the University of Cambridge were invited to ask questions about the Wellcome Trust data management and sharing policy and CRUK data sharing and preservation policy directly of David and Jamie.

This blog is a summary of the discussion, with questions thematically grouped. These questions will be added to the list of Frequently Asked Questions on the University’s Research Data Management Website.

In summary:

  • It is not recommended that researchers simply share a link and release the data when requested. Research data should be available, accessible and discoverable.
  • The first responsibility is to protect the study participants. The funders provide guidance documents on sharing of patient data. Ethics committees also provide advice and guidance on what data can be shared. In principle, patient data should be safeguarded, but this should not preclude sharing. There are models for managed access to data that allow personal/sensitive data to be shared for legitimate purposes in a safe and secure manner.
  • The funders do not want to prevent new collaborations. When sharing data they recommend data generators provide a statement in the description of the data that they are willing to collaborate
  • It is recognised that it is often appropriate for researchers to have a defined period of exclusive access to the data they generate, but this should be determined by disciplinary norms. Any exemptions or delays have to be justified on a case by case basis, ideally at the outset of the project.
  • The funders expect research data that supports publications to be made accessible and publications should have a clear statement explaining how to access the underlying research data.
  • However researchers need to decide what is useful to be shared considering the effort of preparing the data for deposit and of sharing the data. If nobody is going to use the data, sharing is not a good use of researcher’s time.
  • Discipline-specific data repositories, where these exist, are recommended preferentially over general purpose or institutional repositories
  • Biosharing is an excellent resource with references to discipline-specific metadata schemas.
  • Staff members whose role is to manage data is an eligible cost on a grant
  • There are no funds for sharing data from old projects, although there are exceptions on a case by case basis
  • The funders are considering monitoring data management plans but their current primary goal is to encourage people to think about data management and sharing from the very start of the project

Access to research data

Q: Are funders benefiting from the expertise of organisations such as UK Data Service when providing advice on data access? UK Data Service has been managing controlled access to research data for a long time and it would be advantageous to benefit from their expertise.

A: Yes, we are in discussion with the UK Data Service. We are also working with the UK Data Service to consider whether it might be appropriate for hosting data from other disciplines beyond social science. We also believe there is significant scope to share lessons and best practices for data sharing between the social and biomedical sciences.

Q: Could we just share research data only when asked for it?

A: This is not a recommended solution: research data should be available, accessible and discoverable. Data access controls and criteria for what needs to happen for the access to be granted have to be made clear in metadata description.

Q: I have patient data which has to be stored in a secure space. I always say in my data management plan that I cannot share my data. I would like to get ethical guidance which will explain to me how to share these data. It is very easy to say that data cannot be shared. I would like to share my data, but I would like to do it properly. With patient data it is extremely difficult, especially with genomics data, where there is a risk that patients can be identified.

A: Sharing of clinical data is not easy. Both Wellcome Trust and Cancer Research UK are helping to drive a great deal of work which is considering access and governance models through which sensitive patient data can be made available for research in a safe, secure and trusted manner. They provide guidance documents on sharing of patient data. Safety of patients and patients’ data is important. Ethics committees also provide advice and guidance on what data can be shared.

Q: What about sharing of physical materials? I have received a request to share a culture derived from a patient material, but the Ethics Committee did not approve sharing of this material. What shall I do?

A (Peter Hedges, Head of Research Office): If your ethical approval says that you cannot share that material, you cannot share it. Your first responsibility is to protect your study participants.

Q: If I share my data via a repository and people can simply download my data, I can no longer collaborate with them to work on the data and I have lost the possibility of getting credit for my data.

A: Nobody wants to prevent new collaborations from happening. A solution might be to add a statement that you are willing to collaborate in the description of your data. Your data requestor might be interested in collaborating, simply because you know your data the best. Funders also expect that the data re-used by others is appropriately acknowledged/cited, and they want to ensure that due credit results from the secondary use of data.

Quality control of research data

Q: If researchers start sharing unpublished research data via data repositories there is a risk that these data will not be of good quality as they will not be peer-reviewed.

A: Authors of unpublished data can simply state in the data description that the item was not peer-reviewed. If applicable, funders also encourage reciprocal links between publications and supporting research data.

What data needs to be shared and when?

Q: If researchers start to share everything there will be a lot of useless data available in data repositories. How to prevent a flood of useless data on the internet?

A: We would like researchers to decide what data is useful to be shared. If nobody is likely to use the data, sharing is not a good use of researcher’s time. Repositories also need to make decisions over what is worth keeping over time.

Comment (Peter Hedges, Head of Research Office): The Research Council UK focuses on research data supporting publications and this is what we recommend to researchers: share research data which underpins publications.

Q: Are we expected to share large datasets resulting from bigger projects (databases, long-term datasets) or data supporting individual publications?

A: We expect research data that supports individual publications to be made available with a hyperlink to the data. We also want researchers to consider and plan more broadly how they can make data assets of value resulting from our funded research available to others in a timely and appropriate manner.

Q: What about images? Is it useful to share them? It involves a lot of time to organise images. Besides, a single confocal picture with multiple layers is 1GB. In theory it is possible to share all raw data and all raw images, but who would want to look at them? 10 figures of 10 images is already 100 GB of data. Where would I store all these images, who is going to use these data and how am I going to pay for this?

A: The effort of preparing the data for deposit and of sharing the data should be proportionate to the potential benefits of data sharing. Researchers need to decide what is useful to be shared, following disciplinary best practices and norms (recognising that disciplines are in very different places in terms of defining these).

Q: Is there a set amount of time for exclusive use of research data?

A: Researchers should adhere to disciplinary norms. For example, in genomics research data is frequently shared before publication (sometimes under a publication moratorium which protects the data generator’s right to first publication). Any exemptions or delays have to be justified on a case by case basis.

Comment (Peter Hedges, Head of Research Office): Research is competitive. Sometimes it might be useful for researchers to know who wants to get the access to data and what do they need them for.

Cost of data sharing

Q: Can I ask in my grant for a staff member to help me with data management?

A: Yes, this is an eligible cost on grant applications: you can request a salary to support a research data manager for your research project, as long as it is justified.

Q: According to CRUK policy, costs for data sharing can be budgeted in grant applications only from August 2015. What about research data from older projects, when these costs were not eligible in grant applications? Is there any transition fund available to pay for this?

A: Unfortunately, there are no additional funds to pay for these costs. Researchers who have older datasets that might be of significant value to the community should contact CRUK – all requests for support will be considered on a case by case basis.

Q: Wellcome Trust encourages data sharing and data re-use, but does not allow for costs of long-term data preservation to be budgeted in grant applications. This does not make sense to me.

A: We are still reviewing our policy on costs of data management and sharing and we might be revisiting this issue – however, it is problematic for us to consider estimated costs for preservation that extend before the life-time of the grant. Our understanding is that costs of long-term data preservation are often less significant than costs of initial data ingestion by the repository (and we will cover ingestion costs).

Q: Who is then going to pay for the long-term data storage?

A: Wellcome Trust funds some discipline-specific repositories, but this is done jointly with other funders. We support bigger undertakings and we are also working with partners to develop platforms for data sharing and discoverability in some priority areas (notably clinical trials). Cancer Research UK pays for some long-term storage options, if these are justified for particular needs of the project. These decisions are made on a case by case basis, depending on how the costs are justified and whether these are directly related to the scientific value of the project.

Metadata standards

Q: At the moment there are many general purpose and institutional repositories, which are not well structured. To support efficient re-use of data it is important to use structured data repositories and adhere to metadata standards. What are funders’ opinions about this?

A: Wherever possible, discipline-specific data repositories should be used preferentially over general purpose or institutional repositories. Adherence to discipline-specific metadata standards is also encouraged. It has to be acknowledged that development of well-structured data repositories is very resource-intensive and not all disciplines have good quality repositories to support them. For example, it took over 30 years to adapt unified metadata standards at Cambridge Crystallographic Data Centre. The time need to properly solve problems should never be underestimated.

Q: Are funders planning to provide researchers with a list of recommended schemas for metadata?

A: Biosharing is an excellent resource with references to discipline-specific metadata schemas. It is a useful suggestion to include a reference to Biosharing on our website.

Policy implementation

Q: Are you planning to monitor researchers’ adherence to data management plans? For example, the BBSRC does not have the manpower to check all data management plans manually, but they are planning to create a system to check if data has been uploaded automatically.

A: We are considering this. At the moment we require data management plans with the primary goal to encourage people to think about data management and sharing from the very start of the project.

Published 5 February 2016
Written by Dr Marta Teperek, verified by David Carr and Jamie Enoch
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Charities’ perspective on research data management and sharing

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In 2015 the Cambridge Research Data Team organised several discussions between funders and researchers. In May 2015 we hosted Ben Ryan from EPSRC, which was followed by a discussion with Michael Ball from BBSRC in August. Now we have invited our two main charity funders to discuss their views on data management and sharing with Cambridge researchers.

David Carr from the Wellcome Trust and Jamie Enoch from Cancer Research UK (CRUK) met with our academics on Friday 22 January at the Gurdon Institute. The Gurdon Institute was founded jointly by the Wellcome Trust and CRUK to promote research in the areas of developmental biology and cancer biology, and to foster a collaborative environment for independent research groups with diverse but complementary interests.

This blog summarises the presentations and discusses the data sharing expectations from Wellcome Trust and CRUK. A second related blog ‘In conversation with Wellcome Trust and CRUK‘ summarises the question and answer session that was held with a group of researchers on the same day.

Wellcome Trust’s requirements for data management and sharing

Sharing research data is key for Wellcome’s goal of improving health

David Carr started his presentation explaining that the Wellcome Trust’s mission is to support research with the goal of improving health. Therefore, the Trust is committed to ensuring research outputs (including research data) can be accessed and used in ways that will maximise health and societal benefits. David reminded the audience of benefits of data sharing. Data which is shared has the potential to:

  • Enable validity and reproducibility of research findings to be assessed
  • Increase the visibility and use of research findings
  • Enable research outputs to be used to answer new questions
  • Reduce duplication and waste
  • Enable access to data to other key communities – public, policymakers, healthcare professionals etc.

Data sharing goes mainstream

David gave on overview of data sharing expectations from various angles. He started by referring to the Royal Society’s report from 2012: Science as an open enterprise, which sets sharing as the standard for doing science. He then also mentioned other initiatives like the G8 Science Ministers’ statement, the joint report from the Academy of Medical Sciences, BBSRC, MRC and Wellcome Trust on reproducibility and reliability of biomedical research and the UK Concordat on Open Research Data with a take-home message that sharing data and other research outputs is increasingly becoming a global expectation, and a core element of good research practice.

Wellcome Trust’s policy for open data

The next aspect of David’s presentation was Wellcome Trust’s policy on data management and sharing. The policy was first published almost a decade ago (2007) with subsequent modifications in 2010. The principle of the policy is simple: research data should be shared and preserved in a manner which maximises its value to advance research and improve health. Wellcome Trust also requires data management plans as a compulsory part of grant applications, where the proposed research is likely to generate a dataset that will have significant value to researchers and other users. This is to ensure that researchers understand the importance of data management and sharing and to plan for it from the start their projects.

Cost of data sharing

Planning for data management and sharing involves costing for these activities in the grant proposal. The Wellcome Trust’s FAQ guidance on data sharing policy says that: “The Trust considers that timely and appropriate data management and sharing should represent an integral component of the research process. Applicants may therefore include any costs associated with their proposed approach as part of their proposal.” David then outlined the types of costs that can be included in grant applications (including for dedicated staff, hardware and software, and data access costs). He noted that in the current draft guidance on costing for data management estimated costs for long-term preservation that extend beyond the lifetime of the grant are not eligible, although costs associated with the deposition of data in recognised data repositories can be requested.

Key priorities and emerging areas in data management and sharing

Infrastructure

The Wellcome Trust also identified key priorities and emerging areas where work needs to be done to better support of data management and sharing. The first one was to provide resources and platforms for data sharing and access. David pointed out that wherever available, discipline-specific data repositories are the best home for research data, as they provide rich metadata standards, community curation and better discoverability of datasets.

However, the sustainability of discipline-specific repositories is sometimes uncertain. Discipline-specific resources are often perceived as ‘free’. However, research data submitted to ‘free’ data repositories has to be stored somewhere and the amount of data produced and shared is growing exponentially – someone has to pay for the cost of storage and long-term curation in discipline-specific data repositories. An additional point for consideration is that many disciplines do not have their own repositories and therefore need to heavily rely on institutional support.

Access

Wellcome Trust funds a large number of projects in clinical areas. Dealing with patient data requires careful ethical considerations and planning from the very start of the project to ensure that data can be successfully shared at the end of the project. To support researchers in dealing with patient data The Expert Advisory Group on Data Access (a cross-funder advisory body established by MRC, ESRC, Cancer Research UK and the Wellcome Trust) has developed guidance documents and practice papers about handling of sensitive data: how to ask for informed consent, how to anonymise data and the procedures that need to be in place when granting access to data. David stressed that balance needs to be struck between maximising the use of data and the need to safeguard research participants.

Incentives for sharing

Finally, if sharing is to become the normal thing to do, researchers need incentives to do so. Wellcome Trust is keen to work with others to ensure that researchers who generate and share datasets of value receive appropriate recognition for their efforts. A recent report from the Expert Advisory Group on Data Access proposed several recommendations to incentivise data sharing, with specific roles for funders, research leaders, institutions and publishers. Additionally, in order to promote data re-use, the Wellcome Trust joined forces with the National Institutes of Health and the Howard Hughes Medical Institute and launched the Open Science Prize competition to encourage prototyping and development of services, tools or platforms that enable open content.

Cancer Research UK’s views on data sharing

The next talk was by Jamie Enoch from Cancer Research UK. Jamie started by saying that because Cancer Research UK (CRUK) is a charity funded by the public, it needs to ensure it makes the most of its funded research: sharing research data is elemental to this. Making the most of the data generated through CRUK grants could help accelerate progress towards the charity’s aim in its research strategy, to see three quarters of people surviving cancer by 2034. Jamie explained that his post – Research Funding Manager (Data) – has been created as a reflection of data sharing being increasingly important for CRUK.

The policy

Jamie started talking about the key principles of CRUK data sharing policy by presenting the main issues around research data sharing and explaining the CRUK’s position in relation to them:

  • What needs to be shared? All research data, including unpublished data, source code, databases etc, if it is feasible and safe to do so. CRUK is especially keen to ensure that data underpinning publications is made available for sharing.
  • Metadata: Researchers should adhere to community standards/minimum information guidelines where these exist.
  • Discoverability: Groups should be proactive in communicating the contents of their datasets and showcasing the data available for sharing

Jamie explained that CRUK really wants to increase the discoverability of data. For example, clinical trials units should ideally provide information on their websites about the data they generate and clear information about how it can be accessed.

  • Modes of sharing: Via community or generalist repositories, under the auspices of the PI or a combination of methods

Jamie explained that not all data can be/should be made openly available. Due to ethical considerations sometimes access to data will have to be restricted. Jamie explained that as long as restrictions are justified, it is entirely appropriate to use them. However, if access to data is restricted, the conditions on which access will be granted should be considered at the project outset, and these conditions will have to be clearly outlined in metadata descriptions to ensure fair governance of access.

  • Timeframes: Limited period of exclusive use permitted where justified

Jamie suggested adhering to community standards when thinking about any periods of exclusive use of generated research data. In some communities research data is made accessible at the time of publication. Other communities will expect data release at the time of generation (especially in collaborative genomics projects). Jamie further explained that particularly in cases where new data can affect policy development, it is key that research data is released as soon as possible.

  • Preservation: Data to be retained for at least 5 years after grant end
  • Acknowledgement: Secondary users of data should credit original researcher and CRUK
  • Costs: Appropriately justified costs can be included in grant proposals

As of late 2015, financial support for data management and sharing can be requested as a running cost in grant applications. Jamie explained that there are no particular guidelines in place explaining eligible and non-eligible costs and that the most important aspect is whether the costs are well justified or not, and reasonable in the context of the research envisaged.

Jamie stressed that the key point of the CRUK policy is to facilitate data sharing and to engage with the research community, recognising the challenges of data sharing for different projects and the need to work through these collaboratively, rather than enforce the policy in a top-down fashion.

Policy implementation

Subsequently, the presentation discussed ways in which CRUK policy is implemented. Jamie explained that the main tool for the policy implementation is the new requirement for data management plans as compulsory part of grant applications.

Two of the three main response mode committees: Science Committee and Clinical Research Committee have a two-step process of writing a data management plan. During the grant application stage researchers need to write a short, free-form description about how they plan to adhere to CRUK’s policy on data sharing. Only if the grant is accepted, the beneficiary will be asked to write a more detailed data management plan, in consultation with CRUK representatives.

This approach serves two purposes as it:

  • ensures that all applicants are aware of CRUK’s expectations on data sharing (they all need to write a short paragraph about data sharing)
  • saves researchers’ time: only those applicants who were successful will have to provide a detailed data management plan, and it allows the CRUK office to engage with successful applicants on data sharing challenges and opportunities

In contrast, applicants for the other main CRUK response mode committee, the Population Research Committee, all fill out a detailed data management and sharing plan at application stage because of the critical importance of sharing data from cohort and epidemiological studies.

Outlooks for the future

Similarly to the Wellcome Trust, CRUK realised that cultural change is needed for sharing to become the normality. CRUK have initiated many national and international partnerships to help the reward of data sharing.

One of them is a collaboration with the YODA (Yale Open Data Access) project aiming to develop metrics to monitor and evaluate data sharing. Other areas of collaborative work include collaboration with other funders on development of guidelines on ethics of data management and sharing, platforms for data preservation and discoverability, procedures for working with population and clinical data. Jamie stressed that the key thing for CRUK is to work closely with researchers and research managers – to understand the challenges and work through these collaboratively, and consider exciting new initiatives to move the data sharing field forwards.

Links

Published 5 February 2016
Written by Dr Marta Teperek, verified by David Carr and Jamie Enoch
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Could the HEFCE policy be a Trojan Horse for gold OA?

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The HEFCE Policy for open access in the post-2014 Research Excellence Framework kicks in 9 weeks from now.

The policy states that, to be eligible for submission to the post-2014 REF, authors’ final peer-reviewed manuscripts of journal articles and conference proceedings with an ISSN must have been deposited in an institutional or subject repository on acceptance for publication. Deposited material should be discoverable, and free to read and download, for anyone with an internet connection.

The goal of the policy is to ensure that publicly funded (by HEFCE) research is publicly available. The means HEFCE have chosen to favour is the green route – by putting the AAM into a repository. This does not involve any payment to the publishers. The timing of the policy – at acceptance – is to give us the best chance of obtaining the author’s accepted manuscript (AAM) before it is deleted, forgotten or lost by the author.

Universities across the UK have been preparing. Cambridge has had the ‘Accepted for publication? Send us your manuscript‘ campaign running since May 2014 with a very simple and well liked interface allowing researchers to submit their work. The Open Access team then deposits the item, checks for funding and the publisher policies and then organises payment for open access publication if required.

To give an idea of the numbers we are dealing with at Cambridge, during 2015 the Open Access team deposited 2553 articles into our repository Apollo.

Compliance levels

We have been reporting to Wellcome Trust and the RCUK over the past few years to indicate compliance levels with their policies. However the ‘compliance level’ for the HEFCE policy is a slippery concept. For a start, the policy has not yet come into force. Another complicating factor is the long term nature of the ‘reporting’. We will not truly know how compliant we have been until the time comes to submit to REF – whenever that will be (currently it seems 2021).

At Cambridge have been working on the assumption that because we do not know which outputs will be the ones that we will claim we should collect all eligible articles. However, the number of deposited articles Open Access team received over the past year represents approximately 30% of the full eligible output of the University. This might seem concerning in some ways, but it must be remembered that each researcher in the University will only be reporting four research outputs for the REF.

There are some articles that are obvious contenders for REF. By concentrating on researchers who are publishing in very high impact journals we have been trying to catch those articles we are extremely likely to claim.

During the course of 2015 we discovered 93 papers published in Nature, Science, Cell, The Lancet and PNAS. 33% of these papers were already HEFCE compliant. Of the remaining non-compliant papers we contacted 47 authors, made them aware of the HEFCE open access policy, and invited them to submit their accepted manuscript to the Open Access Service. Less than 40% of those authors who were contacted responded with their accepted manuscript. Therefore, even after direct intervention only 49% papers were HEFCE compliant, which means that still more than half of all eligible papers published in Nature, Science, Cell, The Lancet and PNAS during this period would not have been HEFCE compliant had the policy been in place.

The lack of engagement by members of the academic community with this process is a serious concern – and potentially due to four reasons:

  • Lack of awareness of the policy
  • Putting it off until the policy is in place
  • Deliberately choosing not to submit a work because it is not considered important enough or they do not consider their contribution to be significant enough
  • Some form of conscientious objection to the policy

We should note that the third reason is a matter of some concern to the University as it is not the researcher who decides which articles are put forward for REF. In addition, the University is interested in having a high overall level of compliance for REF as it considers making the research output of the institution available to be important.

Temporary reprieve

Cambridge is no island when it comes to facing significant challenges in capturing all outputs in preparation for HEFCE’s policy. While the highly devolved nature of the institution and the sheer volume of publications may be a problem unique to Cambridge and Oxford, other institutions are still developing the technology they intend to use or are facing staffing issues.

In a concession to serious concern across the sector about the ability to meet the deadline, on 24 July 2015 HEFCE announced that there was a temporary modification to the policy. They now allow research outputs to be made open access up to three months after publication until at least April 2017 (and until such time that the systems to support deposit at acceptance are in place).

This means for the first year of the policy we have a small window after publication to locate articles, determine if they are in our repositories, and if not chase the authors for the Author’s Accepted Manuscript.

The trick is knowing that an article has been published. At Cambridge our ‘best bet’ is to use Symplectic which scrapes various aggregating sources such as Scopus. However Symplectic is hindered by the efficiency of its sources. There is no guarantee that a given article will appear in Symplectic within three months of publication. And even if it is, we have already discussed the low engagement by the research community to approaches from the Open Access team for AAMs.

Subject based repositories

So far this blog has been talking about using institutional repositories for compliance. But the policy specifically states: “The output must have been deposited in an institutional repository, a repository service shared between multiple institutions, or a subject repository“.

The oldest, most established subject repository is arXiv.org and it makes sense for us to consider using arXiv as part of Cambridge’s compliance strategy. After all, some areas of high energy physics, most of computer science and much of mathematics use arXiv as a means to share their research papers. In 2014, the number of articles that were deposited into arXiv.org and subsequently picked up in Symplectic and approved by researchers were 582 – approximately 6.5% of Cambridge’s total eligible articles.

If we are able to claim these articles for HEFCE compliance without any behaviour change requirement from our academic staff then this is an ideal situation. But how do we actually do this? There is a footnote to the HEFCE statement above which says that: “Individuals depositing their outputs in a subject repository are advised to ensure that their chosen repository meets the requirements set out in this policy.” And this is the crunch point. arXiv does not currently identify which version of the work has been deposited, nor does it record the acceptance date of the work. Because of this we are currently not able to simply use the work being uploaded to arXiv.

There is work underway to look at this possibility and what would be required to allow us to use the subject based repositories as a means for compliance. HEFCE themselves have identified under ‘Further areas of work‘ that  “measures to support compliance in subject repositories” is an area of uncertainty and they will work with the community to address this.

Alternative approach?

It is possibly a good moment to take a step back from the minutiae of the means and the timing of the HEFCE policy and focus on the goal that publicly funded research is publicly available. We are in a complex policy environment. HEFCE affects all researchers but many researchers are also funded through COAF or the RCUK with their respective (gold leaning) Open Access policies.

Of the HEFCE eligible articles submitted to to Open Access team in 2015, after working through all the different funder requirements, there was a split of 44% gold Open Access and 56% green Open Access. Of the gold payments the split is approximately 74% for hybrid journals and 26% for fully open access journals.  That said, the three journals with which we have published the most – PLOS ONE, Nature Communications and Scientific Reports – are fully Open Access journals with APCs of $1495, $5200 and $1495 respectively.

A highly relevant question is – outside of the efforts by our Open Access compliance teams, how much Cambridge research is being made open access anyway?

Open access articles

The Web of Science (WoS) allows a filter on ‘Open Access’. It does not appear to list articles that are made open access on a hybrid basis, only picking up fully open access journals. While these are not definitive numbers, it does give us some idea of the scale we are looking at. In 2014 WoS gives us a figure of 981 articles published as open access by a University of Cambridge author in a fully open access journal.

The Springer Compact to which many institutions (including Cambridge) have signed up means that now all articles published by that research community will be made open access. In 2014, the Open Access Service had paid for 21 articles to be made open access. In the same period across the institution we had published 695 articles with Springer. (Note that in 2015 we paid 51 Springer  APCs). This means that for the cost of the Springer subscription and our APC payments for the previous year we will have a good proportion of Cambridge articles published as open access articles.

These two sets of numbers only allow for articles published either in fully open access journals or with Springer. It does not account for the articles where the University (or a Department or individual) pays an APC to make an article available in a hybrid (non Springer) journal. The upshot is – a significant proportion of Cambridge research is published open access.

Skip the AAM on acceptance part?

So what does this published open access research mean for compliance with the HEFCE policy? The updated HEFCE policy has addressed this:

“… we have decided to introduce an exception to the deposit requirements for outputs published via the gold route. This may be used in cases where depositing the output on acceptance is not felt to deliver significant additional benefit. We would strongly encourage these outputs to be deposited as soon as possible after publication, ideally via automated arrangements, but this will not be a requirement of the policy.”

This makes sense from an administrative perspective if the article appears in a journal where there is an embargo period on making the AAM available, forcing the University to pay an APC to make the work Open Access to meet RCUK requirements. It would avoid the palaver of:

  • obtaining the AAM from the author
  • depositing it into the repository
  • having to check to see when the article has been published
  • updating the details and
  • either set the embargo on the AAM or change the attachment in the record to the Open Access final published version

However journals where there is an embargo period on making the AAM available forcing an APC payment is in fact almost a definition of hybrid journals. We know there are issues with hybrid – of the extra expense, of double dipping, of the higher APC charges for hybrid over fully Open Access journals. Putting these aside, what this HEFCE policy change means is that publishers have effectively shifted the HEFCE policy away from a green open access policy to a gold one for a significant proportion of UK research. This is a deliberate tactic, along with the unsubstantiated campaign that green Open Access poses a major threat to scholarly publishing and therefore embargoes should be even longer.

We are already facing the problem that hybrid journals are forcing the move towards green open access being ‘code’ for a 12 month delay. This is the beginning of a very slippery slope. We have been outplayed. It really is time for the RCUK and Wellcome Trust to stop paying for hybrid Open Access.

But I digress.

The cons

The message is confusing enough – three sets of policies and three different requirements in terms of the timing and the means to make work compliant and available. We are trying to make it as simple as possible for researchers – with limited success.

The move to widespread Open Access in the UK is a huge shift for the research community and those that support them. It would be very difficult to debate the ‘against’ argument for the statement that publicly funded research should be publicly available but the devil is very much in the detail.

It would be an incredible shame if the HEFCE policy is hijacked into a partial gold OA policy, but as administrators we are drowning in compliance. There needs to be a broad discussion across the funders to try and address the conflicting compliance requirements and the potentially negative effect these policies are having on the future of open scholarly publishing. 

We welcome the opportunity to discuss these issues with HEFCE, Wellcome Trust and the RCUK. There’s plenty to talk about.

Published 25 January 2016
Written by Dr Danny Kingsley
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