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Rather than profiling thousands of individual plasma proteins, we reimagined the plasma proteome as a mixture of amino acid “components.” We identified residues whose abundance shifts markedly during tumour-elicited immune activation.
Each residue is tagged in parallel with a fluorogenic probe that becomes fluorescent only upon covalent reaction. This ensures specificity and eliminates background noise from unreacted dye.
A trained classifier then distinguishes cancer-associated immunosurveillance patterns with high accuracy.
New diagnostics can be designed rapidly, only requiring diagnostic samples with annotated clinical data. We believe there is tremendous untapped potential in our approach. With your help we can impact areas of high unmet need.
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