Vgen23 Blogs

Insights for clinical genomics teams.

Explore research notes, product updates, variant interpretation insights, and practical genomics workflows from Vgen23.

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How to Choose Sequencing Depth

Why the small number after the “x” quietly decides what a genetic test can and cannot find. Authors: Sameer Malik, Sana Most of the times when we connect with a lab to get the gene...

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How AI Is Changing Genetic Testing

How artificial intelligence is changing each step of genetic testing, and why human judgement still has the final say. Authors: Sameer Malik, Sana IN BRIEF For two decades the head...

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How Does Genetic Testing Work?

From a Drop of Blood to a Complete AnswerAuthors: Sameer Malik, SanaThe Question Written in Every CellFor many families, a rare genetic disease begins with years of uncertainty. Se...

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Whitepapers

From Clinical Notes to Clinical Truth: AI-Powered HPO Phenotype Mapping for Precision Variant Prioritization

Authors: Kartik Pal, Dr. Varun Venkat, Dr. Rahila Sardar · Published: 2026 · Reading time: ~12 min Abstract Phenotype-driven variant prioritization is a cornerstone of clinical gen...

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Whitepapers

From Sequencing to Clinical Interpretation: The Infrastructure Gap in Genomic Medicine

Author: Rahila Sardar, PhD — Co-Founder and CEO · Published: April 2026 · Reading time: ~14 min Abstract The cost of whole-genome sequencing reagents has fallen below $300 per geno...

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