Open research data are increasingly recognized as a quality indicator and an important resource to increase transparency, robustness and collaboration in science. However, no standardized way of reporting Open Data in publications exists, making it difficult to find shared datasets and assess the prevalence of Open Data in an automated fashion.
We developed ODDPub (Open Data Detection in Publications), a text-mining algorithm that screens biomedical publications and detects cases of Open Data. Using English-language original research publications from a single biomedical research institution (n = 8689) and randomly selected from PubMed (n = 1500) we iteratively developed a set of derived keyword categories. ODDPub can detect data sharing through field-specific repositories, general-purpose repositories or the supplement. Additionally, it can detect shared analysis code (Open Code).
To validate ODDPub, we manually screened 792 publications randomly selected from PubMed. On this validation dataset, our algorithm detected Open Data publications with a sensitivity of 0.73 and specificity of 0.97. Open Data was detected for 11.5% (n = 91) of publications. Open Code was detected for 1.4% (n = 11) of publications with a sensitivity of 0.73 and specificity of 1.00. We compared our results to the linked datasets found in the databases PubMed and Web of Science.
Our algorithm can automatically screen large numbers of publications for Open Data. It can thus be used to assess Open Data sharing rates on the level of subject areas, journals, or institutions. It can also identify individual Open Data publications in a larger publication corpus. ODDPub is published as an R package on GitHub.
The benefits of openly shared research data (Open Data) for science and society as a whole are manifold, including increases in reproducibility, resource efficiency, economic growth, and public trust in research, as stated e.g. by the Concordat on Open Research Data, drafted by Universities UK, Research Councils UK, HEFCE and Wellcome Trust (The Concordat Working Group 2016). Open Data are increasingly recognized as both an indicator of quality and an important resource that can be reused by other scientists and that can increase transparency, robustness, and collaboration in science (Fecher, Friesike, and Hebing 2015). Several large funders and institutions advocate for Open Data, e.g. the European Commission, NIH, EUA, RDA Europe (Guedj and Ramjoué 2015; NIH 2003; EUA 2017). The Berlin Declaration on Open Access to Knowledge has been signed by over 600 institutions and organizations (“The Berlin Declaration on Open Access to Knowledge” 2003) and the Sorbonne declaration on research data rights was signed recently and is very widely supported (“Sorbonne Declaration on Research Data Rights” 2020). Correspondingly, large infrastructure projects are under way, including the European Open Science Cloud (“EOSC Declaration” 2017). Similarly, Open Code, i.e. analysis code disseminated with the publication, is recognized as an element to further enhance transparency of a study by making available the analysis steps leading from data to results, which is increasingly reflected in journal policies (Stodden, Guo, and Ma 2013).
On the level of individual researchers, Open Data can lead to increased visibility, resource efficiency (Pronk 2019; Milham et al. 2018), and possibly a citation advantage (Colavizza et al. 2020; Piwowar and Vision 2013). However, there are also limits to the open sharing of research data in the biomedical domain, especially when it comes to patient data that are subject to data protection regulations. In those cases, only restricted forms of data sharing involving application procedures and/or de-identification might be possible (Tudur Smith et al. 2015).
Academic institutions have a role to play in incentivizing Open Science by assessing research quality and transparency for the allocation of funds, hiring or promotion. The inclusion of Open Science metrics such as the prevalence of Open Data or Open Code in institutional incentive and reward structures is a necessary step to increase Open Science practices (Strech et al. 2020).
Shared research data allows researchers to find and use already existing datasets. There are currently several databases listing datasets linked to publications. PubMed and Web of Science both provide metadata fields that link shared datasets to publications. Additionally, there are search engines that are specifically focused on openly available datasets, like DataCite, Datamed or Google Dataset Search.
However, there is not yet a standardized way of sharing and reporting Open Data, which makes it difficult to find and link these datasets. Data are currently shared in many different ways, in different field-specific or general-purpose repositories or with data shared as the supplement of a publication. Additionally, the reporting of data sharing is very heterogeneous in the literature. While some journals and publishers like PLoS or BMC have adopted policies on data sharing and introduced mandatory data availability statements, many other journals do not request such statement. This splits the literature into journals in which data availability is relatively easy to check and journals where data availability is not reported in a standardized way. Current studies on data sharing mostly focus on specific journals with mandatory data availability statements (Federer et al. 2018; Colavizza et al. 2020). Open Data may also be shared together with the publication, e.g. in the supplement, or as an independent digital object and cited in the publication (Cousijn et al. 2018; Martone 2014).
As currently only a minority of journals have mandatory data availability statements and the sharing of data as independent digital objects is not common, it is difficult to assess the prevalence of Open Data for the broad biomedical literature. If we want to monitor Open Data prevalence on the level of research fields or institutions, an approach that does not only rely on data availability statements but rather searches the whole publication texts is necessary. Monitoring on the institutional level would also be important to assess the success of an institutional Open Data policy or the effectiveness of incentives for Open Data practices.
In this publication, we develop and validate the text-mining algorithm ODDPub (Open Data Detection in Publications), which screens biomedical publications for Open Data statements. With this approach, ODDPub allows to obtain estimates of the prevalence of Open Data in the biomedical literature on a larger scale and independent of data availability statements. The ODDPub algorithm is freely available as R package on GitHub (https://doi.org/10.5281/zenodo.4071699, RRID:SCR_018385).
Apart from openness as defined by the Open Definition, see (Open Knowledge Foundation 2017), there are other criteria concerning the reusability of datasets, known as the FAIR criteria (Wilkinson et al. 2016). However, few publications would currently comply with the full set of FAIR criteria. Therefore, we used a definition of Open Data that covers only some aspects of the FAIR criteria in addition to the openness criterion.
We only considered research data shared together with a publication. These research data could be raw or preprocessed, but not analyzed or aggregated. Thus, they would allow the analytical replication of the results (or at least a part thereof). However, an imprecision with respect to when data are considered “raw” necessarily remains due to differences in disciplinary practices. Primary data or secondary data (data that is not generated by own experiments but rather by the combination of available data sets, e.g. as part of a meta-analysis) were both eligible, as long as they fulfilled above requirement and the datasets shared were generated by the authors. We considered image data or other audiovisual data only if they encompass a substantial amount of the research data used in the study. In case of doubt, data deposited in repositories were considered Open Data due to their findability and potential reusability, while conversely data in supplementary materials were only considered Open Data if these were clearly raw data. We excluded audiovisual data that are primarily shared for illustrative purposes. The amount of data was not a criterion for inclusion per se, such that data from a study with a handful of subjects were still considered Open Data.
We used similar criteria for Open Code, and counted a publication as Open Data/Code publication if:
We specifically did not address all possible kinds of data sharing statements. We explicitly excluded cases of data sharing where a registration or application is necessary to access the data. While cases of restricted access to data can have good reasons, for example for clinical datasets, this is out of the scope of the current work, which only considers Open Data. We also excluded cases of data being available upon request. Making data available upon request is considered a suboptimal data sharing strategy and several studies (Savage and Vickers 2009; Rowhani-Farid and Barnett 2016; Naudet et al. 2018) have shown that in many of those cases data cannot be accessed, especially after longer periods of time (Vines et al. 2014).
We created two training sets and a validation dataset for the development of the algorithm.
The first training dataset consisted of the institutional publications record of the Charité -Universitätsmedizin Berlin from the years 2015 to 2017. To retrieve the publication record, we searched the publication databases PubMed and Embase for publications with affiliations that matched a list of keywords with variations of the institutional name (see Supplementary File S1). Additionally, we filtered the results for the publication years 2015-17 and for the publication type ‘journal article’ (PubMed) or ‘article’ (Embase). We obtained 9896 results from PubMed and 9256 results from Embase. The resulting publication lists from both databases were then combined and duplicates were removed by matching the DOI, PubMed ID (PMID), or the title and the last name of the first author. The combined publication list consisted of 11192 entries. To retrieve the publication PDFs, we loaded the combined publication list into EndNoteTM (Version: X8.2, https://www.endnote.com) and used the ‘Find full text’ function. That way, 8689 (78%) of the publications could be retrieved. Some full texts could not be retrieved from journals for which our institution has no access (see Figure 1).
The second training dataset consisted of publications randomly selected from all publications listed in PubMed in the year 2018. For this, we downloaded a list of all PMIDs from 2018 by exporting the search results using the following search filter:
We retrieved a list of 1091518 PMIDs from which we randomly sampled 1500 (0.14%) IDs. We again downloaded the full texts and were able to retrieve 992 (66%) publications. As the PubMed metadata on the publication type was not always correct, we manually checked the publication types of the downloaded full texts. We excluded publications with the article types Editorial, Comment, Letter to Editor, Review, Erratum, Guideline, Historical Article, Case report. Additionally, we excluded other non-research articles that did not fit in any of those categories (e.g. Question & Answer) and research articles that were out of the scope of the biomedical literature (social science & history of science). After excluding those publication types, we were left with 868 publications (see Figure 2).
This dataset was originally planned as the validation dataset, but due to low sensitivity of the algorithm developed on the institutional publication record, we decided to use this second dataset to improve the algorithm further. We then drew another sample of N = 1400 publications (downloaded full texts: 964, 69%, after publication type check: 792) listed in PubMed in the year 2018 that was used as the final validation dataset (see Figure 3).
To prepare the publications for text mining we performed a number of preprocessing steps. Using an R script, we first converted the PDFs to text files using the poppler library (Poppler (version 0.67.0) 2018). We then loaded the text files into R and split the texts into the individual sentences using the “tokenizers” R package (Mullen et al. 2018). As the last step, the text was converted to lowercase.
To establish a gold standard for the Open Data detection in the training and validation samples, we manually screened the publications for Open Data. The screening followed a standardized procedure, involving the following steps:
A more detailed description of the manual search strategy can be found in supplemental file S2.
To estimate the interrater reliability of the manual screening, a second rater checked 100 publications from the validation dataset independently. For this, we chose a random sample of 25% of all positively identified Open Data papers (n = 21) and added a random sample of n = 79 negatively identified papers to partially even out the strong class imbalance in this dataset. Both raters used the manual screening procedure as defined above to determine the Open Data status (either “true” or “false”) for each of the 100 publications independently. We then calculated the percentage of cases where the raters agreed in their assessment of the Open Data status of the paper. If the agreement between raters had been too low, the interrater reliability check would have been extended to a larger sample, including all positively identified cases. However, no prespecified threshold was defined for this. For the 100 publications of the validation dataset that were checked by two independent raters, an agreement regarding Open Data status was reached in 95% of the cases. Due to the high degree of agreement, we decided that no further extension of the double check was necessary. For details on the interrater sample see supplemental file S6.
For the development of ODDPub, we used an iterative procedure to manually derive and refine a set of keywords and key phrases to detect Open Data statements, focusing on first increasing the sensitivity and subsequently increasing the specificity in each step. As we could not check all publications in our first training sample manually for Open Data and as the prevalence of Open Data was rather low, we focused on analyzing all positively detected cases as well as a random subset of the negatively detected cases during the first iterations. We give a brief summary of the development procedure here. A more detailed description can be found in supplemental file S3. For details on the different algorithm stages, see supplemental files S4 and S5 as well as the GitHub repository (https://doi.org/10.5281/zenodo.4071699).
We started with a small number of confirmed Open Data publications. We extracted all keywords or key phrases relevant for the Open Data status and wrote an R script that uses regular expression matching to search for the keywords in the sentences of the preprocessed publication texts. If any of the keywords was detected, the publication was counted as hit.
We applied this first version of the keyword search to the whole Charité training dataset (N = 8689 publications). We manually checked samples from the positively detected cases as well as from the negative cases. Using the information from the false positive and false negative cases, we improved the algorithm by adding new keywords and forming keyword groups of which several have to match in the same sentence. This was repeated for three rounds, where the algorithm was again applied to the whole training dataset after each improvement and samples of positive and negative cases were manually assessed to further improve the keyword groups and to decrease the false positive and false negative rate of the algorithm.
Among the keyword groups were groups that comprised names of repositories as well as their accession numbers. In those keyword groups we entered all the repositories that we found at least once among the detected Open Data cases in the publications of the training dataset. Additionally, we added repositories that were in the following two repository lists: 1) a list of the 20 most common repositories from a large analysis of data availability statements of PLoS One publications from Federer et al. 2018 and 2) a list of repositories recommended by the data journal Scientific Data (Scientific Data 2020), from which we only included the biomedically relevant journals.
We then applied the improved algorithm to the first random sample of 992 PubMed publications. First, we manually searched all publications in the sample for Open Data, where we detected 98 (9.9%) Open Data publications. Then we ran the algorithm on the same publication sample and compared the results to the gold standard of manual search. We found a sensitivity of 45% and a specificity of 98%. As we considered a sensitivity of 45% insufficient, we decided to use this first PubMed sample to improve the algorithm further and to draw a second PubMed sample as the final validation sample. In a final round of improvement, we used the manually detected Open Data statements from the first PubMed sample that were missed by the algorithm to add new keywords and keyword categories for improved coverage of the algorithm. Additionally, we used the false positive cases to remove keywords that primarily led to false positive detections. Detailed information on the final version of ODDPub can be found in supplemental file S4.
We applied the final version of our algorithm to all publications of the validation dataset and compared the results with the manual screening results using the sensitivity, specificity and F1 score as performance measures.
As an additional benchmark, we also extracted the associated metadata on the datasets recorded in the databases PubMed and Web of Science for all publications in the validation sample. For PubMed we used the metadata field ‘Secondary Source ID’, which contains database names and dataset identifiers of datasets associated with the publications. Those databases comprise many genetic databases as well as the general-purpose databases Dryad and Figshare. For Web of Science we used the associated datasets that were linked to the publications of the validation sample. Those can be found as an additional linked field “Associated Data” under the title of a publication on the Web of Science website.
We calculated the number of datasets listed in the metadata field that were also found by ODDPub as well as the number of listed datasets that were missed by ODDPub.
The resulting text-mining algorithm has a hierarchical keyword structure and searches for several categories of similar keywords in each sentence (see Figure 4). We grouped similar keywords identified in the statements indicating open data or code from the training dataset into categories (see supplemental file S4). Examples are the categories FIELD_SPECIFIC_DB, containing database names like “Gene Expression Omnibus”, “Sequence Read Archive”, or “Protein Data Bank” and AVAILABLE, containing words to denote that the data have been made available, like “deposited”, “released”, or “submitted”. The explanations in this section hold true for the detection of both Open Data and Open Code.
Groups of several keyword categories were then formed that each comprise several keyword categories. Those groups of keyword categories cover different ways of data sharing like field-specific repositories, general-purpose repositories or deposition of data in the supplement (see Table 1). For a match in a group of keyword categories, at least one of the keywords in each underlying keyword category has to match. For the example of the “Field-specific databases” category group, we need matches for any of the keywords of the underlying categories FIELD_SPECIFIC_DB, AVAILABLE and ACCESSION_NR (which contains regular expressions to match the accession numbers of those databases). There are two types of keyword category groups. Either all keywords are searched within the same sentence or the keywords are searched across sentence borders, allowing for a maximum number of other words between the keywords. This is necessary in cases like “S2 Table. Raw data. (XLS)”, where the information is spread across sentence borders. The whole text of the publication is checked for a match in any of the keyword category groups. A publication is categorized as Open Data if any of the keyword category groups match for at least one passage in the full text. All details on the categories see supplemental file S4 or the GitHub repository (https://doi.org/10.5281/zenodo.4071699).
|Combined Keyword Categories||Explanation|
|Field-specific repositories||Checks if data deposition in field-specific database and accession number is mentioned|
|General-purpose repositories||Checks if data deposition in general-purpose database that uses no accession number is mentioned|
|Dataset||Checks if dataset that is given specific number (e.g. “dataset S1”) is mentioned|
|Supplemental table or data||Checks if a numbered file or table or raw data is mentioned together with specific file formats|
|Supplementary raw/full data with specific file format||Checks if raw/full data is mentioned together with specific file formats|
|Data availability statement||Checks if an accession number or a repository name is mentioned in the data availability section|
|Dataset on GitHub||Checks if data deposition on GitHub is mentioned|
|Data journals||Checks journal DOI for certain known data journals|
|Source-code availability||Checks if availability of source code is mentioned|
|Supplementary Source-code||Checks if source code in the supplement is mentioned|
In addition to the Open Data status, the algorithm outputs the sentence in which the Open Data statement was detected. This allows a fast manual check of the results in cases where removal of the remaining false positives is crucial. Also, it allows to use the detected Open Data statements for further analysis (e.g. on details of how data are shared).
In this section, we report the performance measures of ODDPub for the validation dataset. For this, we compared the results from the manual screening to the results obtained with ODDPub.
In the manual search Open Data was detected for 11.5% (n = 91) of the publications in the validation dataset and Open Code was detected for 1.4% (n = 11) of the publications.
The results of the Open Data prediction for ODDPub compared to the gold standard of manual screening can be found in Table 2. We obtained a sensitivity of 0.73, a specificity of 0.97, and a F1–score of 0.73. The results of the Open Code prediction for ODDPub compared to the gold standard of manual screening yield a sensitivity of 0.73, a specificity of 1.00, and a F1–score of 0.64 (see Table 3).
To check if any Open Data publication found by ODDPub was missed by the manual screening, we manually checked the Open Data statements of all 24 publications detected with ODDPub but not with the manual screening. We identified one of those 24 publications as Open Data publication according to our definition and counted it as an Open Data publication in Table 2. The remaining 23 publications turned out to be false positive detections (see Table 5).
As only few cases of Open Code were found, the estimates for the performance metrics for the Open Code detection are unreliable. Two Open Code publications were only found by ODDPub and not by the manual screening. As for the case of Open Data, we manually verified the Open Code status of these publications and counted them as Open Code publications in Table 3. Of the six false positive cases, there are five cases of Open Code reuse.
Next, we compared our results to the linked datasets found in the databases PubMed and Web of Science (see Figure 5).
For the comparison with PubMed we retrieved the entries in the ‘Secondary Source ID’ field in PubMed for the 792 publications in the validation sample. We found that 19 of those publications have an entry in the secondary ID field. 11 of the entries referred to clinical trial registration IDs (8 on ClinicalTrials.gov, 3 on ISRCTN). Four entries linked to a Figshare dataset, two linked to a Dryad repository, and one entry linked to the Genbank and the Protein Data Bank, respectively. All Figshare and Dryad datasets were also detected by ODDPub. The two entries for Genbank and the Protein Data Bank were both cases of reuse of previously published data. Those do not fit our definition of Open Data and were not detected by ODDPub.
For the comparison with Web of Science, we retrieved the datasets linked in Web of Science for the 792 publications in the validation samples. We found that 11 publications have reported associated data. Those fall into the following categories:
Of those 8 reported datasets, 6 were found by both ODDPub and manual search. The PDB dataset was only found by manual search and one of the CCDC datasets was found by neither ODDPub nor the manual search. Only the link to the Dryad repository could be found through both PubMed and Web of Science.
In summary, both PubMed and Web of Science linked only few of the datasets found by ODDPub for the publications in the validation sample.
To determine which categories of Open Data were most frequently discovered, we categorized all 91 manually detected Open Data publications of the validation dataset in the following categories: supplemental data, field-specific repository, general-purpose repository (including GitHub), institutional repository, data journal, and personal/project-specific website. One publication can be assigned to multiple categories if applicable.
Most of the detected Open Data publications used either the supplement or a field-specific repository (Table 4). Of the 24 manually detected Open Data cases that were not found by ODDPub, there were 17 cases with supplemental data and 7 cases with field-specific repositories. Sharing data via the supplement was thus less likely to be detected by the algorithm.
|Category||Number of occurrences|
|General-purpose repository (including GitHub)||14|
Additionally, we categorized the 23 false positive cases detected by ODDPub in the validation sample (see Table 5). Most of the cases were not labeled as Open Data in the manual search because our definition of Open Data was not fulfilled in some way. In three cases, the algorithm made a major mistake and detected a statement that was not related to data sharing at all. In one case, an Open Data publication that was missed by the manual search was detected.
|Category||Number of occurrences|
|Shared data not raw data||9|
|Data sharing with restrictions||4|
|Open Data reuse||4|
|Only analysis code shared||3|
|Detected sentence not related to data sharing||3|
|Data available upon request||1|
|Linked OSF repository was empty||1|
|Case of Open Data missed by manual search||1|
A list of all detected Open Data statements for the training and validation datasets as well as the results of the manual screening can be found in a separate OSF repository (https://doi.org/10.17605/OSF.IO/YV5RX).
In this work, we developed a text-mining algorithm that can screen biomedical publications for mentions of Open Data sharing, as well as the provision of self-developed code (Open Code). Our text mining algorithm allows to screen large numbers of publications for statements indicating Open Data sharing automatically.
An advantage of our approach compared to other studies that focus on specific journals that have a dedicated data availability statement (Federer et al. 2018; Colavizza et al. 2020) is the broader applicability. As our algorithm screens all parts of a publication, Open Data statements can be detected anywhere in the text. This allows screening of publications in journals without dedicated data availability statements. A disadvantage of this approach is that this makes the task more complex compared to an approach that only focuses on the data availability statements. The studies of (Federer et al. 2018; Colavizza et al. 2020) both could use a less complex classification algorithm on the data availability statements, which is not possible when searching the full text.
Compared to the two currently available publication databases PubMed and Web of Science that do link information on Open Data to publications we could show a much better coverage of our algorithm on the validation dataset. This suggests that currently our approach is superior to the other available approaches for the automated detection of Open Data publications from a larger publication corpus.
ODDPub has several possible areas of application. One area is the large-scale assessment of data sharing rates, for example on the level of different subject areas, where a manual assessment is too time-consuming and where a strategy relying on data availability statements alone is not possible due to many journals that have not yet implemented those statements.
Another possible area is the detection of individual Open Data publications in a larger publication corpus, e.g. to identify the Open Data publications of a specific research institution. This can be necessary if the institution wants to distribute additional performance-oriented funding for publications with Open Data. In this case, the output of the detected Open Data statements by the algorithm helps to gain more details on the detected publications and allows for a fast manual check for false positives. We used ODDPub in a semi-automated way (automated screening plus manual check) for the detection of Open Data publications in the Charité publication body among researchers eligible for the annual allocation of performance-based funding. In 2019 over 120.000 Euros were allocated among Charité researchers based on semi-automated Open Data detection, and this is planned to be continued in 2020 (Kip et al. 2019; BIH 2019).
Open Data is a fast-evolving field, with some but yet few standards. Therefore, the provided results on specificity and sensitivity are a snapshot in time, and might change quickly. The algorithm will require further and continuous development and adaption to the changes and developments in the field, e.g. new repositories and the wider adoption of data availability statements.
One of the main limitations is the sensitivity of 73% obtained for the current version of ODDPub. The missed Open Data publications might be problematic in applications where a very high coverage of Open Data publications is important. As most of the missed Open Data publications shared supplemental data, this problem might be reduced in the future if more research data are shared through repositories.
Our approach focuses on the detection of open research data that are linked to a publication. For an assessment of datasets published independently of a publication, a different approach would be necessary.
Additionally, the scope of our algorithm was the biomedical literature and many of the Open Data statements found by the algorithm refer to repositories specific to the biomedical domain. The performance on other research areas has not been tested and one can expect a decrease in performance of the algorithm when applied to other research areas. The accessibility of journals is another limitation. As not all journals were accessible to us, we could not include those into our training dataset. Due to this, we could have potentially introduced a bias in our training dataset and missed additional relevant repositories or keywords.
Importantly, our definition of Open Data did not require data to be FAIR (Wilkinson et al. 2016) or complete. Thus, even in the manual check, which we used as a gold standard, the standards of data provision were set very low. Indeed, while we could not quantify the fraction of reported findings for which raw data had been shared, providing the data underlying all results was surely rather exception than norm. Similarly, standards of machine-readability and documentation in our Open Data sample clearly fell short of multiple FAIR criteria for most datasets, even though this was not systematically assessed. Thus, Open Data sharing rates reported here will not be comparable with those detected applying more stringent criteria of completeness and reusability, which would be recommendable to do as Open Data sharing becomes more common and standardized.
For the detection of Open Code, one obstacle is that the standardization of Open Code statements is still lower than for Open Data (e.g. no database IDs). Both the lower standardization and the lower prevalence of Open Code combined make it difficult to develop a robust tool for Open Code statement detection.
How Open Data is deposited and linked will change over time, with new data repositories emerging and changing file formats. Thus, the algorithm needs to be adapted in the future to keep up with these developments. One possibility would be to update all repositories listed in e.g. re3data.org and FAIRsharing.org automatically to keep the algorithm up to date regarding available repositories. However, ODDPub was developed given the current landscape of Open Data, in which solutions for reusable Open Data sharing and standardized, automated detection of the datasets are already present, but have not yet been universally adopted. These include in particular
Another relevant point concerning the citation of datasets in the future is the distinction between citations of newly generated datasets and of re-used datasets. In our screening, we observed that Open Data reuse can create confusion with the sharing of primary data when detecting these practices by text mining. Thus, data citation principles and corresponding metadata fields in registries need to assure that the sharing of primary data and the reuse of data can be distinguished. In addition, granting access to data under restrictions is another important way of data sharing especially in biomedical research. Practices of definition, annotation and detection need to consider this, and provide the necessary information in a machine-readable fashion, if the current definition of Open Data is to be maintained.
In conclusion, the text-mining algorithm ODDPub presented in this study can detect sharing of raw data (‘Open Data’) in publications from the biomedical literature. It can detect different ways of sharing Open Data, like field-specific repositories or sharing of raw data in the supplement. The results of the validation of the algorithm indicate that it finds the majority of Open Data publications in the current system of how Open Data are shared and linked in the biomedical literature. In the future, our method can be used to assess data sharing rates in the biomedical literature on a larger scale, which would not be possible with a manual approach.
The ODDPub algorithm is available as R package on GitHub (https://doi.org/10.5281/zenodo.4071699, RRID:SCR_018385) under the MIT license. A dataset containing information on the publications used in the training and validation datasets, including the publication DOIs, the results of the manual screening and the extracted Open Data statements can be found under https://doi.org/10.17605/OSF.IO/YV5RX.
The additional files for this article can be found as follows:Supplement S1
Search queries for the databases PubMed and Embase. DOI: https://doi.org/10.5334/dsj-2020-042.s1Supplement S2
Detailed description of the procedure for the manual search for Open Data statements in the publications. DOI: https://doi.org/10.5334/dsj-2020-042.s2Supplement S3
Detailed description of the algorithm development procedure. DOI: https://doi.org/10.5334/dsj-2020-042.s3Supplement S4
Table with a detailed description of the keywords used in each of the different versions of ODDPub. DOI: https://doi.org/10.5334/dsj-2020-042.s4Supplement S5
Table with the detailed evaluation of the results of each algorithm development stage that were used to inform the next version of the algorithm. DOI: https://doi.org/10.5334/dsj-2020-042.s5Supplement S6
Results of the interrater reliability sample. DOI: https://doi.org/10.5334/dsj-2020-042.s6
We thank Meggie Danziger, Maxim Benz, Claudia Kirchert and especially Yasmin Aktas for their help with the manual screening of publications. Additionally, we thank Lisa Liebenau, Florian Beng and Clemens Blümel for the helpful discussions in the early conceptual phase of this project. Finally, we thank Benjamin Gregory Carlisle and Ulrich Dirnagl for their helpful comments on our manuscript.
N.R., E.B. and M.K. designed the study. N.R. wrote the software package and performed the data analysis. N.R. and E.B. contributed to the validation of the algorithm. N.R. wrote the manuscript in consultation with E.B. and M.K.
The authors have no competing interests to declare.
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