Centogene at ASHG 2026
Oct 20–24, 2026 Montréal, Canada ~7.5k attendees Website
Centogene brings 3 presentations to ASHG 2026 in Montréal, and exhibits at Booth 1301. Its program centres on rare-disease diagnosis, reproductive carrier screening, and genome sequencing at ASHG 2026. Centogene presents short-read sequencing for complex carrier variants, genome sequencing for CAG-repeat ataxias, and Ultima Genomics sequencing in challenging rare-disease cases.
| Organization | ASHG 2026 Attendance |
|---|---|
Centogene Rostock, Germany | 1 Senior Product Manager · 1 Vice President Medical Genetics · 1 Chief Medical and Genomic Officer |
CENTOGENE sells clinical genetic diagnostics and genomic knowledge software to physicians, patients, and pharma partners.
| Booth Exhibiting at Booth 1301 Wed, Oct 219:45am–4:30pmThu, Oct 229:45am–1:30pmFri, Oct 239:45am–4:30pm Poster Wed Oct 21 2:30 pm Short-read genome sequencing as a one-test approach in reproductive genetic carrier screening for the detection of complex gene variants. Exome/genome sequencingReproductive geneticsVariant callingMendelian disorder Poster Wed Oct 21 2:30 pm Genome sequencing as a diagnostic tool for hereditary spinocerebellar ataxias caused by CAG repeat expansions AtaxiaDiagnosticsExome/genome sequencingLaboratory genetics and genomics Poster Thu Oct 22 4:15 pm Evaluation of Ultima Genomics whole-genome sequencing for rare disease diagnostics in challenging variant contexts BioinformaticsDiagnosticsSequencing technology |
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