Valid-NEO: Multi-omics Pipeline for Neoantigen Assays

Valid-NEO: Multi-omics Pipeline for Neoantigen Assays

2022–Direct Identification and Quantification of Neoantigens from Minute Amount of Clinical Biopsy Sample — published on Cancers

In recent years, neoantigens are becoming popular cancer therapeutic targets under intensive studies by almost all major oncology pharmaceuticals. However, who are the target patients? Does the patient with a “correct” mutation and a “correct” HLA allele indeed present the “correct” neoantigen? Is this individual’s neoantigen copy number high enough for immunotherapy? AI predictions based on NGS genomic information have been proven incapable of answering these questions. Immunopeptidome through mass spectrometry is dominated by disease-irrelevant peptide sequences.  There is no existing way to identify and quantify neoantigens from a minute amount of clinical biopsy sample, such as 50 mg tissue or less. Valid-NEO is developed to fit this demanding clinical need through combining our proprietary multi-omics platforms including NGS-based ultra-rare mutation calling technique, DEEPER-SeqS, and our unique clinical proteomics platform, Complete360®, with additional hardware innovations (Ref. 1).

  1. Publication: Valid-NEO: A Multi-Omics Platform for Neoantigen Detection and Quantification from Limited Clinical Samples.
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