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Choose a method

FiberPhotometry is organized around the scientific question, not the name of an algorithm. Choose the row that describes what you want to learn; each category then separates supported workflows, experimental workflows, and known gaps.

A scientific question routes to signal validity, event-locked responses, spontaneous dynamics, multi-signal relationships, population inference, or behavioral and longitudinal integration.
Start with the estimand. Acquisition and quality checks precede every route; population inference and robustness apply across routes rather than replacing them.
Your question Start here Typical output
Is the fluorescence trace technically and biologically interpretable? Signal formation and validity corrected signal, QC ledger, validity status
What happens around an event, or what does each overlapping event explain? Event-locked responses and encoding peri-event contrast or held-out encoding kernel
What events, rhythms, or states occur without a supplied event clock? Spontaneous and continuous dynamics transient ledger, PSD, autocorrelation, spectrogram, state contrast
How do sites, colors, or spatially arranged fibers relate? Multi-signal and spatial analysis association, coherence, crosstalk review, spatial summary
Does an effect generalize across animals and analytic choices? Population inference and robustness animal-level interval, mixed-model sensitivity, multiverse ledger
How do pose, behavior, sessions, and learning trajectories connect? Behavior and longitudinal integration synchronized annotations, comparable session summaries, Unspool handoff

Two maps with different jobs

Method availability is not evidence of scientific validity. Every empirical page must identify the experimental unit, uncertainty denominator, assumptions, and the strongest claim its evidence permits.

Cross-cutting rules

  1. Preserve acquisition clocks, gaps, channels, and annotation provenance.
  2. Separate signal construction from the scientific outcome.
  3. Hold out complete animals or sessions when evaluating prediction.
  4. Aggregate repeated measurements before population inference.
  5. Name defensible alternatives and retain failed workflows.
  6. Treat figures, tables, and machine-readable artifacts as views of the same versioned result.