Genomics

VarPath-Clin

VarPath-Clin is a SYNTHETIC/DEMO genomics model for clinical variant pathogenicity classification. Outputs are deterministic demo values — NOT for clinical use. Trained (synthetically) on de-identified sequence data.

Sequence PathAI Community License: Apache-2.0 v3.2.1 RTG 4.3 DL 131,078
SYNTHETIC DEMOAll outputs are deterministic demo data — not for clinical use, not real medical inference.

Metrics

MetricValueSplit
AUC0.976Synthetic hold-out
Calibration (ECE)0.025Synthetic
InputsOutputs
VCF variant recordACMG class + score

Run a synthetic prediction

Returns a deterministic synthetic result — clearly labeled, not for clinical use.

API integration

Call this model from your pipeline (demo — no real key required):

import requests
r = requests.post("https://api.biofoundry.ai/v1/models/bf-025-varpath-clin/predict",
    headers={"Authorization": "Bearer <API_KEY>"},
    json={"input": "<vcf variant record>"})
print(r.json())  # -> synthetic demo prediction

See the API reference · JSON: /api/models/bf-025-varpath-clin

Version history

VersionStatusNotes
v3.2.0ArchivedSynthetic release note 0
v3.2.1CurrentSynthetic release note 1

Community contributions: 128 synthetic contributors have submitted evaluations and fine-tunes.