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    BioPhi quickstart

    Call biophi_humanness for an OASis score and class, or biophi_humanize and biophi_graft to return a humanized VH/VL with the mutations made.

    You have an antibody VH/VL pair and you want to know how human it is — and, if it isn't human enough, a humanized version that keeps the CDRs. BioPhi does both: paste the sequences, pick a mode, submit, and read the OASis score or the humanized sequence off the result card.

    Score or humanize

    Provide VH (and VL)

    Paste the heavy-chain variable-region sequence, and the light chain too if you have it. Or name a known therapeutic and let the platform resolve the VH/VL from Thera-SAbDab.

    Pick which tool to call

    Call biophi_humanness to only score, biophi_humanize to rewrite the sequence with the Sapiens model, or biophi_graft to humanize by CDR grafting — the mode follows from which one you call. For humanization, set a target humanness; biophi_humanize also lets you toggle whether known binding residues stay fixed.

    Submit and wait

    BioPhi runs as an asynchronous CPU job on Modal. Submit it, and a result card appears on the canvas when the job finishes.

    Read the result

    In scoring mode the card shows the OASis humanness score, percentile, and human/humanized/chimeric/murine class, broken down per CDR and framework. In humanization mode it also shows the humanized VH/VL and the mutations made.

    In chat

    Describe the antibody and what you want done — the model routes to BioPhi and chains numbering, repertoire mining, or stability around it.

    What to do next

    • Confirm manufacturability — run antibody developability on the humanized candidate, since humanization can shift charge and aggregation.
    • Number the humanized sequence — run ANARCI to re-annotate CDRs.
    • Cross-check with a second metric — score the same sequence with Humatch.

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