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Diana L. Thomas

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Open access Oct 2026

Optical genome mapping identifies clinically relevant somatic structural variation in epilepsy-affected brain tissue.

Somatic variants are a prominent cause of epilepsy-associated cortical malformations, but about half of patients undergoing genetic testing have no finding due partly to limitations in variant detection. Most studies have focused on single-nucleotide variants or small indels that are accessible to short-read sequencing...

Anthony R. Miller, James J. Anderson, Maria E. Hernandez Gonzalez et al. · 0 citations

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