analyse rare disease NGS data
in minutes
analyse rare disease NGS data
in minutes
Moon helps diagnosing patients at:
“Moon has accelerated our diagnostic process. It is not only fast but also very up to date: we diagnosed cases with pathogenic mutations in genes that were just published as disease genes. With Moon, yesterday’s publication is today’s diagnosis.”
Prof. dr. Frank Baas, MD
Head, Laboratory Diagnostic Genome Analysis
Leiden University Medical Center, The Netherlands
“Moon is a real added value to our diagnostic pipeline for NGS: very user-friendly, performant and up-to-date with the newest data from the recent literature.”
Prof. dr. Geert Mortier, MD
Chairman, Department of Medical Genetics
Antwerp University Hospital, Belgium
“In whole exome and genome sequencing, variant interpretation is a big challenge. Moon can provide the disease-underlying variant(s) with a few clicks in a couple of minutes, even among a large number of whole-genome variants. As a medical geneticist, I really appreciate Moon’s speed and easy HPO-based workflow. Moon helps us to diagnose rare diseases, presenting clinically important variants we should not miss.”
Dr. Gabor Matyas, PhD, FAMH Medical Genetics
Head, Swiss Foundation for People with Rare Diseases
Zentrum für Kardiovaskuläre Genetik und Gendiagnostik, Switzerland
Give Moon a try with your own samples.
Click "Try now" for a web-based demo and a Moon trial account that will allow you
to analyse your own WES or WGS data.
supporting rare disease diagnostics
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