Vaccine & T-cell developers

myPATHOGEN

Infectious disease target discovery - AI-guided pathogen antigen selection

myPATHOGEN is a dedicated computational workflow for infectious disease antigen discovery. It combines sequence-conservation analysis with neoMS presentation prediction, neoIM immunogenicity prediction, and population-coverage optimization. The workflow prioritizes CD4+ and CD8+ T-cell targets that remain conserved across viral, bacterial, and parasitic strains.

What myPATHOGEN delivers

The end-to-end myPATHOGEN workflow has a turnaround time of eight weeks:

  • Genome-wide association studies → linking pathogen genetic variation to phenotypes such as virulence, drug resistance, or immune evasion
  • Conservation analysis: prioritization of immunogenic epitopes within conserved regions
  • Presentation prediction: identification of surface-presented epitopes in populations infected with different strains
  • Immunogenicity prediction: identification of presented epitopes recognized by immune cells
  • myCONSTRUCT: next-generation string-of-beads design (optional)
  • myRNA: next-generation codon optimization (optional)

Frequently asked questions about myPATHOGEN

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What is myPATHOGEN?

myPATHOGEN is a dedicated computational workflow for infectious disease antigen discovery. It combines sequence-conservation analysis with neoMS presentation prediction, neoIM immunogenicity prediction, and population-coverage optimization. The workflow prioritizes CD4+ and CD8+ T-cell targets that remain conserved across viral, bacterial, and parasitic strains.

What is the turnaround time for myPATHOGEN?

The end-to-end myPATHOGEN workflow has a turnaround time of eight weeks. Required data and deliverables are confirmed for each project.

Can myPATHOGEN feed into construct design?

Yes. Selected myPATHOGEN targets can proceed to myCONSTRUCT for multi-epitope construct design and myRNA for codon optimization.