immunogenicity
Estimate how likely a protein therapeutic is to provoke an anti-drug antibody response, and locate the sequence regions responsible. Use this skill to tile a sequence into peptides, predict class II MHC presentation across a population-representative allele panel, aggregate predicted binders into a per-region and whole-molecule risk score, compare a candidate against its closest human germline, and decide which liabilities are worth deimmunising. Also trigger on immunogenicity, anti-drug antibody, ADA, T-cell epitope, MHC class II, HLA-DRB1, NetMHCIIpan, NetMHCpan, deimmunisation, tregitope, or population coverage.
- Version
- 1.0
- License
- MIT
- Compatibility
- Requires Python 3.10+. The bundled scripts tile sequences, parse NetMHCpan/NetMHCIIpan output, and aggregate epitope burden using only the standard library. Running the predictor itself needs NetMHCIIpan or NetMHCpan from DTU Health Tech, which is free for academic use but requires a signed licence and is not redistributable.
Pinned to revision f67572246d9b, so it is the text this page describes rather than whatever the author pushed since.
Pre-approved tools experimental
Experimental field. Support varies between clients, so this list is what the author declared, not what your client will enforce.
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Files
- skills/immunogenicity/SKILL.md
- skills/immunogenicity/references/deimmunisation.md
- skills/immunogenicity/references/running-netmhciipan.md
- skills/immunogenicity/references/what-drives-ada.md
- skills/immunogenicity/scripts/ada_risk.py
- skills/immunogenicity/scripts/epitope_scan.py
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