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Updated: May 23, 2025

Characterizing Mutational Load and Clonal Composition of Human Blood
Published on: July 11, 2019
An artificial intelligence-based model for prediction of clonal hematopoiesis variants in cell-free DNA samples
Gustavo Arango-Argoty1, Marzieh Haghighi2, Gerald J Sun2
1Oncology R&D, AstraZeneca, Waltham, MA, USA. gustavo.arango@astrazeneca.com.
Abstract:
Circulating tumor DNA is a critical biomarker in cancer diagnostics, but its accurate interpretation requires careful consideration of clonal hematopoiesis (CH), which can contribute to variants in cell-free DNA and potentially obscure true tumor-derived signals. Accurate detection of somatic variants of CH origin in plasma samples remains challenging in the absence of matched white blood cells sequencing. Here we present an open-source machine learning framework (MetaCH) which classifies variants in cfDNA from plasma-only samples as CH or tumor origin, surpassing state-of-the-art classification rates.
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