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Explore breakthrough studies in transcriptomics, epigenetics, and genome editing techniques driving functional genomics forward.

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Decoding a Genetic Mystery: The Novel RUNX1 Mutation Transforming Our Understanding of Inherited Blood Disorders

Explore the discovery of a novel 3' mutation in RUNX1 gene and its implications for familial platelet disorder and leukemia predisposition.

Aurora Long
Nov 01, 2025

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