CAELVERIS
Evidence report
CAELVERIS benchmark and source status
Public siteEvidence overview

Benchmark charts

Summary charts for ranking outcomes and evidence-source visibility.

This page shows the demo evidence packet, ranking performance and source status. This software benchmark is not a diagnosis and does not replace clinical validation.
Evaluated cases
300
Hit@1
96.0%
Hit@5
99.3%
Precision@5
27.7%

Ranking visibility

Causal at rank 1
96.0%
Causal in top 5
99.3%
F1@5
42.4%

Benchmark metric profile

The same demo metrics are shown together so ranking quality is readable at a glance.

Hit@1Hit@5Precision@5F1@5100%50%0%
Benchmark summary only; these values do not represent a patient-level probability.

Evidence layer availability

ClinVar
AVAILABLE
GenCC
AVAILABLE
HPO / MONDO / Orphanet
AVAILABLE
gnomAD
OPTIONAL
Bars show source state in this demo snapshot, not allele frequency.

Pipeline stage status

FASTQ / input QC
READY
Alignment QC
READY
Variant QC
READY
VEP + evidence
READY
Ranking + report
READY
This is the demo artifact state; uploaded clinical runs can have different QC gates.

Evidence sources

SourceStatusDescription
ClinVarAVAILABLELocal GRCh38 SQLite evidence store
GenCCAVAILABLEGene-disease validity
HPO / MONDO / OrphanetAVAILABLEPhenotype and disease normalization
gnomADOPTIONALPopulation frequency is enabled per run configuration

Real demo run

HG002_1000 / GRCh38 / VEP, ClinVar and gnomAD source statuses are retained in report metadata.

ChartsEvidence overview