PeptOdyssey
Precision Peptide Genomics

Your Genome.
Your Peptide Map.

Upload your genetic data and discover which peptide therapies align with your unique biology. Variant-level analysis across 11 candidate therapies, powered by 7 annotation engines.

Start Analysis

How It Works

01

Upload

Drop your genome file — VCF, 23andMe, or CSV format.

02

Annotate

Cross-referenced against ClinVar, gnomAD, VEP, UniProt, PharmGKB, and GWAS Catalog.

03

Predict

Peptide therapy response prediction based on pathway and receptor genetics.

04

Report

Clinically prioritized variant report with per-peptide gene variant mapping.

11 Peptide Therapies Evaluated

Each therapy is mapped to its target genes. Your variants are matched to predict response, efficacy, and safety considerations.

BPC-157

Multi-Pathway Regenerative

27 target genes

Thymosin Alpha-1

Immune Modulation

3 target genes

CJC-1295 + Ipamorelin

Growth Hormone

1 target gene

Epithalon

Longevity / Telomere

1 target gene

AOD-9604

Weight Management

1 target gene

MOTS-c

Metabolic

1 target gene

Plus Matrixyl, Argireline, SNAP-8, GHK-Cu + BPC-157 + TB-500, and BPC-157 + TB-500 combination therapies.

7 Annotation Engines

Ensembl VEPNCBI ClinVargnomADMyVariant.infoUniProtPharmGKBGWAS Catalog

Results are cached across sessions — repeated variant queries resolve instantly from the local database.

Begin Your Analysis

Upload a genome file to generate your personalized peptide therapy report.

Drag & drop or click to choose

.vcf, .txt, .csv — max 100 MB

Comma-separated. Used for drug–drug–gene phenoconversion (e.g. paroxetine converts CYP2D6 normal metabolizers into poor metabolizers).

Genome files are encrypted in transit and at rest and are automatically deleted within 24 hours of job completion.

PeptOdyssey

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