Johns Hopkins Medicine, All Children's Hospital, USA
"Alamut Visual has dramatically improved our research capabilities and our testing workflow related to both NGS and Sanger based tests. We wouldn't want to imagine a world without it.
Alamut Batch is an intuitive, comprehensive and cost-effective solution to annotation."
Cincinnati Children's Hospital Medical Center, USA
"We are very grateful for the work you do with Alamut and continuing to improve it. We use it on daily basis to help us interpret variants for clinical tests including our technicians, analysts, genetic counselors and lab directors. Alamut has the comprehensive information available for interpreting variants and great documentation. I’ve recommended Alamut to many customers who ask me about the tools that I use. Many thanks to you for making this possible."
PASCALE RICHARD M.D. Ph.D.
"We were early Alamut adopters and this software has become essential to our daily diagnosis lab practice, saving time and reducing mistakes. The intuitivity of use and the new functionalities are a very useful help in our daily work."
Invitae, San Francisco, USA
"We have found Alamut to be an immensely useful tool, and would recommend Alamut to anyone looking for a powerful yet straightforward software program that is able to accurately catalogue and evaluate mutations."
HELGE ROOTWELT M.D. Ph.D.
Oslo University Hospital, Norway
"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."
JORDAN LERNER-ELLIS, Ph.D.
Mt. Sinai Hospital, Toronto, Canada
"Alamut is the best tool I have used for the annotation of DNA variants. It has a great user interface, combines data from multiple sources and allows for ease of variant interpretation by clinical geneticists."
KATE THOMSON, FRCPath
Cardiac Service Oxford University Hospitals, UK
"Alamut enables us to interrogate and manage our data with ease. It has an intuitive interface, which brings together a range of routinely used resources, saving a significant amount of time & ensuring a consistent approach to variant interrogation."
PROF. MILAN MACEK Jr. M.D. Ph.D.
Charles University, Prague
"We are very pleased with Alamut since it conveniently streamlines post-sequencing analyses of detected variants. We value the programme user friendliness and its all-in one approach to variant analysis."
HONEY V REDDI Ph.D., FACMG
The Jackson Laboratory, Farmington, USA
"I have used Alamut visual for the past five years and it has been an invaluable resource to me as a Molecular Geneticist."
EDGARDO R. PARRILLA, MD
Duke University, Durham, USA
"I recommend Alamut to all of my colleagues and friends in genomics!"
ATCLearn, Salmiya, Kuwait
"I tried different software applications that are available in the market before I made my final decision. I must say alamut visual is the best in many ways, and sometimes you feel like you enjoy to surf in software and it makes you feel more and more curious with your findings in the data you work with. Thank you!"
Wellington Regional Genetics Laboratory, Wellington, New Zealand
"I have previously used Alamut Visual in the UK and it is an invaluable resource for variant curation which I was keen to bring into use in my new role in New Zealand. provides a convenient and user-friendly interface which pulls together literature searches, population databases and in silico prediction tools. This enables streamlining of the curation process and saves a lot of time."