PubMed · 14589559
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R Dean. 1989. Editorial: software survey section.. https://doi.org/10.1016/0887-6177(89)90012-7
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Precision oncology relies on integrating tumour fraction, variant allele frequency, clonal haematopoiesis of indeterminate potential assessment, pathogenicity, and clinical context into next-generation sequencing interpretation, enabling biologically informed and clinically meaningful treatment decisions while reducing the risk of overinterpreting nontumour or nonactionable genomic alterations.