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We exhibited at the Assises de Génétique Humaine et Médicale meeting which took place in Nantes, 24-26 January 2018.

Thank you for visiting us on booth n°22, we presented you our solutions in term of annotation, filtration and interpretation of human genome variants, with the Alamut software suite

Alamut Batch : the high throughput annotation engine for NGS variants
Alamut Focus : the interactive filtration tool for annotated variants
Alamut Visual : the decision-support software application for variants interpretation, in diagnostics and research

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What they say
about Alamut

"In developing new genetic assays and evaluating the implications of newly identified sequence variations, Alamut helps me work faster and safer to ensure and document quality in assay design and interpretations."

HELGE ROOTWELT M.D. Ph.D.
Oslo University Hospital, Norway

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