Dr. Didgar Research Institute

Research glossary

40 research terms with concise definitions and practical guide links, from CI and TOST to FAIR and Registered Reports.

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40

Estimand
The quantity a study aims to estimate for a defined population, condition and time; not simply a test name.
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Confounding
A causal structure that distorts an exposure–outcome comparison relative to the target effect; adjustment requires assumptions and timing.
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p-value
Under a specified null model, the probability of data at least as incompatible with that model; not the probability that the null is true.
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Confidence interval (CI)
An interval produced by a procedure with specified long-run coverage under its assumptions; not automatically a probability for the observed interval.
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Standard error (SE)
Uncertainty of an estimator across sampling repetitions; different from individual-data variability or SD.
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Standard deviation (SD)
A measure of value dispersion; specify sample/population definition and units.
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Smallest effect size of interest (SESOI)
A meaningful-effect threshold justified scientifically or practically with explicit units before results.
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Two one-sided tests (TOST)
An equivalence procedure against two bounds; failure to reject a difference test does not substitute for it.
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Statistical power
Probability of rejecting a null under a specified effect and design scenario; inseparable from its assumptions.
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Missing completely at random (MCAR)
An assumption that missingness is independent of observed and unobserved values; not implied by a small missing percentage.
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Missing at random (MAR)
Missingness does not depend on missing values after conditioning on suitable observed information.
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Missing not at random (MNAR)
Missingness remains related to unobserved values beyond an MAR assumption; sensitivity matters.
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Preregistration
A time-stamped record of plans and decisions, with prior-data access disclosed and changes/exploration distinguished.
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Registered Report (RR)
A publication format reviewing the design before results with conditional later stages; registration alone is not that review.
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In-principle acceptance (IPA)
A Stage 1 Registered Report decision with conduct/reporting conditions; not unconditional acceptance of any later work.
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Multiverse analysis
Transparent examination of defensible decision-dependent paths; counting significant paths is not a scientific vote.
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Computational reproducibility
Recreating output from specified data, code and environment; distinct from a new-data replication.
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Replication
A new-data investigation with suitable design to examine robustness or scope.
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FAIR principles
Findable, accessible, interoperable and reusable; not necessarily unrestricted data openness.
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Data dictionary
Variable definitions, units, types, ranges, missingness and provenance needed to interpret data.
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Data management plan (DMP)
A plan for production, protection, documentation, access and preservation with actual responsibilities and restrictions.
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Digital Object Identifier (DOI)
A research-object identifier; syntax alone establishes neither existence, correctness nor scientific quality.
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ORCID researcher identifier
A researcher identifier reducing name ambiguity; not an assessment of work quality.
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Preprint
A publicly available manuscript before journal publication with its actual review status stated.
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Accepted Author Manuscript (AAM)
The accepted manuscript incorporating review revisions before publisher typesetting; deposit rights need checking.
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Version of Record (VoR)
The formal publisher-record version, distinct from an AAM or preprint.
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Data Descriptor
An article type focused on provenance, quality and data reuse under outlet-specific requirements.
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Constraints on Generality (COG)
A statement of populations, settings, stimuli and times covered by evidence and conditions for expected extension.
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PRISMA review reporting
A family of review-reporting guidance; a reporting format alone does not validate review conduct.
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Living systematic review (LSR)
A review with planned ongoing surveillance, update decisions, versions and a stopping policy.
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CONSORT trial reporting
Randomized-trial reporting guidance; check the 2025 version and design-appropriate extensions.
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SPIRIT trial protocols
Guidance on trial-protocol content, distinct from reporting actual results.
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CHART health-chatbot reporting
Guidance for evaluating generative-chatbot health advice and responses within a specific scope.
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COREQ qualitative reporting
Reporting guidance for interviews and focus groups; applicability depends on the actual method.
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TOP 2025 transparency
A transparency and verification framework; keep version and evidence levels distinct from earlier criteria.
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Researcher reflexivity
Documented attention to researcher position, assumptions and decisions in producing and interpreting data.
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Sensitivity analysis
Examination of conclusions under defensible alternative assumptions or decisions, not selection of a preferred result.
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Risk of bias
Potential distortion from design or conduct, distinct from journal reputation or anonymous review.
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Similarity and attribution
Tool matches require text interpretation; an aggregate percentage is not an automatic misconduct decision.
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Quarto computational document
A document connecting code and narrative; dependencies and output verification still matter.
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