NeuroKit2

Scope and evidence cutoff

Use this skill for method-aware, reproducible biosignal research with NeuroKit2. The snapshot was checked on 2026-10-01 against:

• stable PyPI 0.2.13, released 2026-03-02;
• Python metadata (>=3.10; classifiers 3.10–3.14) and wheel dependencies;
• GitHub release notes/tags, NEWS.rst, source at tag v0.2.13;
• official API pages/examples (the live site identified itself as 0.2.13.dev214); and
• pinned 0.2.13 runtime signatures and synthetic output schemas.

The current wheel requires pandas<3.0.0. The refreshed core checks use Python 3.13, NumPy 2.5.3, and pandas 2.3.3; forcing pandas 3 conflicts with upstream metadata. API fragments below assume caller-provided arrays and imports. Optional MNE source reconstruction, cvxEDA, EMD, and pyRQA paths are source-reviewed, not runtime-validated by this refresh. Synthetic checks establish software behavior, not empirical validity.

The live documentation can be ahead of the stable wheel. Prefer the pinned runtime for reproducible work and name both versions if consulting development docs.

Boundary

NeuroKit2 is a research and educational toolbox. Do not present its output as:

• a diagnosis, treatment recommendation, patient-monitoring decision, or alarm;
• validation, certification, or regulatory evidence for a medical device; or
• proof that a physiological construct is measured validly in a new sensor, protocol, environment, population, or disease group.

Validate acquisition hardware, electrode/optode placement, units, sampling and clock accuracy, preprocessing, detector/decomposition method, population, task, and outcomes for the intended study. Preserve raw data and an auditable exclusion log. Use deidentified local files only; do not place PHI in prompts, logs, examples, or bundled fixtures.

Reproducible installation

uv pip install "neurokit2==0.2.13"

For optional features, create a uv project, add only the packages actually required at reviewed exact versions, and commit/review the resulting uv.lock before uv sync --locked. NeuroKit2 exposes an upstream full extra, but this skill intentionally does not install that floating transitive set in an automated workflow. Optional capabilities can require MNE, cvxopt, Plotly, PyEMD, pyRQA, Pillow, OpenCV, or file readers. Record the resolved environment with the analysis. Provision any MNE data/template download as an explicit, checksummed study input. Do not install a moving development branch for a reproducible study.

Required data contract

Before processing, record:

1. signal identity and sensor/channel configuration;
2. native sampling rate in Hz and physical unit (or explicitly arbitrary_unit);
3. clock, timestamp origin, drift correction, and synchronization evidence;
4. polarity/orientation and acquisition-side filters/gain;
5. missing samples, discontinuities, saturation, flatlines, motion, and annotations;
6. whether event onsets are zero-based sample indices or seconds;
7. planned preprocessing order, methods, parameters, exclusions, and outputs; and
8. participant-level grouping needed to prevent leakage in later statistics.

Never infer units from a column name. Do not silently treat samples as milliseconds, volts, microsiemens, or arbitrary units.

Core workflow

1. Inspect before transforming

python skills/neurokit2/scripts/inspect_signal.py \
  --input recording.csv --root . --deidentified \
  --columns ECG,RSP,EDA --time-column time_s \
  --units ECG=mV,RSP=a.u.,EDA=uS

The inspector is bounded and emits no row values or paths. Resolve non-monotonic time, duplicate samples, gaps, non-finite values, flat runs, and sampling-rate disagreement before filtering.

2. Preserve preprocessing order

Use this default reasoning order, adapting it to the acquisition and cited method:

1. preserve immutable raw signal and annotations;
2. verify time base, units, polarity, clipping, gaps, and artifacts;
3. segment at long gaps; only interpolate short gaps under a declared policy;
4. apply modality-specific cleaning at the native sampling rate;
5. detect peaks/onsets or decompose components;
6. inspect quality outputs and raw overlays;
7. correct peaks only with logged categories and sensitivity checks;
8. derive rates/features;
9. align continuous modalities on a declared common time grid; and
10. map event indices to that grid, epoch, baseline, and analyze.

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