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Comprehensive genomic profiling improves diagnostic precision in sarcomas, guiding treatment decisions.
Conclusions: Comprehensive genomic profiling improved diagnostic precision and revealed rare, oncogenically meaningful, and potentially targetable events.These findings highlight the role of NGS in guiding risk stratification, therapeutic selection, and clinical-trial matching in ultra-rare sarcomas.
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Bozkurt et al. (2026) studied this question.
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