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Discretization of Blood-Based Infrared Fingerprints Reveals Biomarker-like Variables for Efficient Multi-omics Integration

Kosmas V. Kepesidis1,2,3,*, Nico Feiler1,2, Vasileios Papalampropoulos1, Michael Trubetskov2, Andreas Döpp1,2, and Ferenc Krausz1,2,3,†

  • *Contact author: kosmas.kepesidis@lmu.de
  • †Contact author: ferenc.krausz@mpq.mpg.de

PRX Life 4, 023001 – Published 1 April, 2026

DOI: https://doi.org/10.1103/8x56-xvyh

Abstract

We present a methodology that leverages the zero-crossing time gaps of electric-field molecular fingerprints from liquid biopsies to extract information about their molecular composition. By analyzing zero-crossing timings, we demonstrate that these temporal features encode all medically relevant information contained in the original time traces. A clinical study targeting lung cancer detection using human blood samples reveals that aberrations in zero-crossing time gaps are associated with the presence of the disease and its progression. The proposed approach to discretizing continuous molecular signals through zero-crossing analysis enables compact representation of physiological signatures and can facilitate integration with other omics technologies, opening pathways for comprehensive, multidimensional biological insights.

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