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Hematopoietic clone-derived mutations, including 'driver mutations' and 'passenger mutations', are prevalent in the cf-DNA of both healthy individuals and cancer patients and may be a potential source of false positives in the liquid biopsy. Our results also suggest the ineffectiveness for distinguishing clonal hematopoietic mutations of low VAF (≤0.1%) from tumor-derived mutations using conventional next-generation sequencing of blood cell DNA. However, an error correction model with an ultralow error rate and high coverage depth is required for blood cell DNA sequencing, which is difficult and costly to achieve with current technologies.
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Liu et al. (Thu,) studied this question.
www.synapsesocial.com/papers/699ea8a3d8a7e1a4e1facfe6 — DOI: https://doi.org/10.1093/annonc/mdy513
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
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Annals of Oncology
South China University of Technology
BGI Group (China)
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