05EVALUATION PLAN

Evidence before performance claims.

The design defines a controlled comparison of fusion strategies. Measured accuracy, latency and throughput results have not yet been published.

Current status: planned evaluation. No percentages or illustrative scores on this site should be read as experimental results.
01COMPARATIVE EXPERIMENTS

The same evidence. Different policies.

Subject-disjoint evaluation and fixed validation/test splits are planned. C, C-Q and D are compared using the same module outputs and mandatory safety gates so the effect of quality and attack rules can be assessed separately.

Planned comparison configurations
CONFIGURATIONPURPOSEROLE
A · Face onlyIdentity-only diagnostic controlOffline baseline
B · Face + PADMeasure the contribution of visual PADOffline baseline
C · L1Fixed-weight full-channel fusionShared gates
C-QQuality-weighted full-channel fusionShared gates
D · L2Quality- and attack-aware fusionShared gates + pattern rules
L3ML-assisted advisory modelOffline evaluation
02WHAT WILL BE REPORTED

Security, usability and cost—together.

Security outcomes

Attack acceptance and genuine-user rejection, separated by attack type and evaluation protocol. PAD-layer APCER and BPCER are reported with their applicable protocol.

Coverage & retries

ACCEPT, REJECT and RETRY distributions for genuine and attack attempts, definitive-decision coverage and technical failures.

Runtime behaviour

Latency and resource usage under declared capture and deployment profiles. Short-window rPPG uncertainty is reported explicitly.

Physical presentation attacks and digital input injection are evaluated separately. ISO/IEC 30107-3 terminology is a design reference; the project does not claim certification or full standards conformance.

FROM DESIGN TO IMPLEMENTATION

Explore the thinking behind BioAuth.

Read the architecture, evidence contracts and experimental design.