July 23rd, 2026
The Missing Half of NIPT
NIPT is no longer defined by sequencing alone. The next phase depends on trustworthy interpretation, patient-specific reporting, and scalable informatics that clinicians can actually use.
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A space to share perspectives on genomics, precision medicine, and digital health—ranging from technical notes on variant interpretation to reflections on accreditation and laboratory informatics.
June 16th, 2026
The invisible Half of a Clinical Laboratory
How a first-in-province NGS launch, a clinical accreditation, and a pile of spreadsheets led me to build SHELF.
Read more →May 14th, 2026
The Long Tail of Actionable Cancer
The Evolution and Impact of Comprehensive Genomic Profiling (CGP) on Cancer
Read more →November 21st, 2025
A Practical Primer on Clinical Variant Interpretation
This primer walks through the evolution of clinical variant interpretation—from the early days of ambiguous terminology to the modern era of consensus guidelines—and contrasts germline and somatic frameworks while outlining best practices and future directions in precision oncology.
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