Transparency & Data Policy (pubar-transparency-and-data)
PAR endorses the Center for Open Science's Transparency and Openness Promotion (TOP) Guidelines and
has adopted transparency standards for authors (检索于 2026-06;以官网为准). Build the materials as you
go so a transparency request at review or acceptance does not stall the paper.
When to trigger
- Building the reproducibility / transparency materials and the data-availability statement
- A reviewer or editor requested data, code, or documentation
- Data cannot be fully shared (privacy, FOIA limits, agency restrictions, IRB) and you need the path
- Deciding whether to pursue pre-registration badges
What PAR's TOP standards cover (verify current wording)
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Data & materials citation. Cite all research materials and data sources used, with persistent
identifiers where available — treat data as a citable research output.
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Data sharing. PAR encourages depositing data in an appropriate repository — Dataverse for
quantitative data, the Qualitative Data Repository (QDR) for qualitative data — with a
data-availability statement in the manuscript.
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Reporting documentation. PAR recommends documenting research design, data preparation, and
analysis decisions in a supplementary document, following the relevant reporting standard where
applicable (e.g., CONSORT for experiments, STROBE for observational, PRISMA for reviews, COREQ for
qualitative).
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Pre-registration. Pre-registration of studies and/or analysis plans is supported, and
badges may be available — register before data collection/analysis (see
pubar-research-design).
Build-as-you-go checklist
Transparency package by evidence type
Build the package around the evidence product, not around a generic folder dump.
| Evidence type |
Minimum package |
PAR-specific risk |
| Administrative microdata |
Data dictionary, construction log, access conditions, replication code, and an approved restricted-data statement if raw data cannot ship |
A practitioner-facing claim with no auditable data provenance |
| Survey / experiment |
Instrument, sampling frame, recruitment/consent language, randomization code, preregistration or exploratory label, and cleaning scripts |
Treatments or outcomes cannot be interpreted by public managers |
| Qualitative interviews / fieldwork |
Interview protocol, coding scheme, memo trail, anonymized excerpts or controlled-access deposit, and IRB/consent constraints |
Over-disclosure that harms participants, or under-documentation that blocks audit |
| Case comparison / process tracing |
Case-selection memo, source inventory, evidence tests, chronology, and rival-explanation log |
"Illustrative" cases presented as field-wide lessons |
| Public datasets / dashboards |
Persistent links, download dates, version snapshots, transformation scripts, and archived outputs |
Live web data change after review and no longer reproduce the exhibits |
Restricted-data decision tree
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Can raw data be public? Deposit the exact analysis data plus code in Dataverse or another
persistent repository and cite it in the Data Availability Statement.
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Can de-identified analysis data be public? Deposit the de-identified data and document what
was removed, masked, top-coded, aggregated, or perturbed.
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Can synthetic or toy data run the code? Provide synthetic data plus a validation note that the
code path reproduces the tables/figures but not the confidential estimates.
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Can only metadata be shared? Provide a data-access route, DUA/IRB constraints, variable list,
and a read-only replication log that maps each exhibit to the restricted source.
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Is nothing shareable? Treat this as an editor-facing exception request; explain why the claim is
still auditable and which independent checks remain possible.
For every restricted path, separate legal/ethical inability from convenience. Convenience is
not a transparency rationale.
When data cannot be shared (restricted-data path)
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Explain why the data are restricted (privacy, IRB, agency/legal restrictions, FOIA limits).
- Provide instructions on how others can obtain the data (access process, agency contact, DUA).
- Where feasible, provide synthetic data or de-identified extracts so the code can be run.
- For qualitative data, QDR supports controlled-access sharing with appropriate protections.
Reproducibility smoke test
Before submission, run a clean-room check:
- start from a fresh directory or container with only the repository/deposit files;
- install from the recorded environment file;
- run the master script end to end;
- compare every printed table/figure number against the manuscript;
- record any manual step, proprietary software dependency, or restricted-data substitution.
If the smoke test fails, do not call the package "reproducible"; report the remaining limitation
honestly in the Data Availability Statement.
Anti-patterns
- Treating transparency as a post-acceptance afterthought
- Depositing code that does not actually reproduce the printed tables/figures
- A personal URL or dead link instead of a persistent repository (Dataverse/QDR)
- Claiming data are restricted with no access path or synthetic substitute
- Undocumented, un-seeded, unpinned code that "works on my machine"
Output format
【Repository】Dataverse (quant) / QDR (qual) — materials staged? [Y/N]
【Evidence type】admin / survey-experiment / qualitative / case-process / public-dataset
【Reproduces tables/figures?】master script verified locally? [Y/N]
【Documentation】README + provenance + seeds + pinned versions + reporting standard? [Y/N]
【Data-availability statement】drafted? [Y/N]
【Restricted data?】public / de-identified / synthetic / metadata-only / exception request
【Smoke test】fresh-run status + remaining manual step
【Pre-registration】badge pursued? [Y/N/NA]
【Next】pubar-review-process
Supplementary resources