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A novel software package for detection and analysis of rare genomic variants
Value Proposition· Clinical Genomics Gap Addressed: This technology directly targets the systematic underdetection of rare pathogenic germline variants by current industry-standard pipelines, a gap with direct consequences for hereditary cancer diagnosis, trial enrollment, and treatment eligibility.· Novel Ensemble Approach: Rather than...
Published: 7/24/2026
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Inventor(s):
Jun Luo
,
Daniel Rabizadeh
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Category(s):
Technology Classifications > Research Tools
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Technology Classifications > Computers, Electronics & Software
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