Events in 2026

There is a busy conference year coming up, so make sure to check out the dates, mark your calendars and join us for some exciting sessions and workshops.

In 2025, Limbus has teamed up with Nostos to combine the comprehensive long- and short-read analysis with the varvis® software and the AI-powered variant interpretation and classification with AION. Together, we will be hitting the road in 2026 to showcase this unique combination, but also to discuss the latest developments and advancements in clinical genetics and to learn more about your workflows and needs.

April 23–24: SSMG, Annual Meeting of the Swiss Society of Medical Genetics —Lausanne, Switzerland

End of April we will be back in Switzerland and will join the annual meeting of the Swiss Society of Medical Genetics. Together with team Nostos, we can’t wait be able to get in touch with the Swiss human genetics community for interesting sessions and insights, discussions and exchange.

Meet us at Booth #11.

June 13–16: ESHG — Annual meeting of the European Society of Human Genetics — Gothenburg, Sweden

As always, we round up the first half of the conference year with the biggest European conference in the field of human genetics, the ESHG annual meeting. This year, we will go up north and meet in Gothenburg, Sweden. We are looking forward to four days packed with workshops, lectures, poster sessions, meetings and conversations with the human genetics community.

Get your appointment calendars and already mark a slot to visit us at our booth #516 to discover the new features we have in store for you. Also, note Saturday, June 13, when we invite you to our lunch Corporate Satellite.

Where to find us? Booth #516

What not to miss? Corporate Satellite “This is the way: Bringing long-read data analysis to clinical routine” June 13, 2026–12:15–13:30

A Hitchhiker’s Guide to LRS: Implementing long-read sequencing in clinical diagnostics Dr. Denny Schanze, University Hospital Magdeburg

Beyond simple variant detection: Maximizing the clinical utility of long-read sequencing Dr. Ben Liesfeld, Limbus Medical Technologies GmbH

September 17–18: NVHG/BeSHG — Joint meeting of the Dutch & Belgian Societies of Human Genetics — Rotterdam, Netherlands

This year, the Dutch and Belgian Societies of Human Genetics are joining forces and will be meeting for the annual conference in Rotterdam. Of course, we can’t miss this opportunity, and Team varvis® and Team Nostos will be there to present our comprehensive long-read analysis solution, new features and developments. Join us at the booth or at our corporate talk!

Stay tuned for more information soon.

October 7–9: SIGU — XXIX Congresso nazionale SIGU 2026 — Rimini, Italy

SIGU in Rimini has been a blast last year and we are already looking forward to seeing you again this year in exactly the same place! But don’t worry, we won’t be presenting you with exactly the same things. A lot has happened, and we can’t wait to show you the features and improvements we’ve been working on over the past few months.

Visit us at booth #42 for exciting news & join us for our workshop on Wednesday, October 8, 13.00–14.00.

More details coming soon!

November 2–4: LRUA — Long-Read Sequencing Uppsala, Sweden

Under the motto ‘Empower your research with long-read sequencing technologies’, the Swedish and international human genetics community is gathering in Uppsala to catch up with the latest developments in long-read sequencing technologies and their applications, get inspired by peers presenting their research, and enjoy discussions with leading experts and company representatives. Stay tuned for more details and meet team varvis® in Uppsala!

Past events

January 15, 2026: User Group Meeting — Göttingen, Germany

During our regular User Group Meeting, our varvis® users had the opportunity to get an exclusive sneak preview of upcoming features, share interesting cases, and engage in an open discussion and exchange. This year, we had a special guest joining us for a keynote, Paralympic champion Elena Semechin, and we were happy to announce our partnership.

January 27–30, 2026: Annual Meeting of the French Society of Human and Medical Genetics — Cannes, France

We started the new year at full speed, when the red carpet was rolled out for the French human genetics community in Cannes at the annual meeting of the FFGH (Fédération Française de Génétique Humaine). We hosted an industry symposium, “Vers une génomique clinique de nouvelle generation”, on the second day of the conference. 📺 You can now watch the recording of the workshop 👉 here.

____ Lunch symposium “Vers une génomique clinique de nouvelle generation”

Comment l’IA révolutionne-t-elle la génomique clinique?​ Dr Aina Pi Roig, Nostos Genomics GmbH

**Turning complexity into clarity: Automated long-read sequencing analysis​ **Dr Ben Liesfeld, Limbus Medical Technologies GmbH

T2T vs. hg38: Vers une nouvelle norme Rolf Schröder, Limbus Medical Technologies GmbH

March 4–6: GfH, Annual Meeting of the German Society of Human Genetics — Munich, Germany

Every spring, the German human genetics community meets at the annual meeting of the GfH for three days packed with interesting lectures, workshops and discussions on the latest developments and news in clinical genetics.

Team varvis® and team Nostos were at the scene and showcasing what’s new and what’s next in the varvis® software, incl. long-read whole genome sequencing, now also available for ONT data and the integration of AI-powered variant interpretation by AION.

April 15–17: AEGH, V Congreso Interdisciplinar en Genética Humana — Granada , Spain

¡Nos vemos en la maravillosa España! More precisely, in lovely Granada, ur team attended the annual meeting of the Spanish Society of Human Genetics and held a workshop about long-read data analysis and artificial intelligence in clinical diagnostics.

Workshop “Transformando el diagnóstico clínico: Lecturas largas e Inteligencia Artificial” April 16, 2026–13:30–14:20

Introducción — El software varvis®: una plataforma todo-en-uno para el análisis de NGS Ana De las Peñas, Limbus Medical Technologies GmbH

Las lecturas largas han llegado para quedarse: Cómo el software varvis® facilita el análisis de datos complejos. Dr Aina Pi Roig, Nostos Genomics GmbH

Nuevos horizontes genómicos: la IA en el diagnóstico clínico Dr Rocío Acuña, Nostos Genomics GmbH

April 17: Flanders Nanopore Day — Antwerp, Belgium

The Flanders Nanopore Day in April brought together researchers, scientists, and industry professionals interested in nanopore technology and its applications.

Our managing director Dr. Ben Liesfeld, gave a presentation that showcased some interesting long-read cases.

**Time to say goodbye: long-read sequencing ready to replace array diagnostics in clinical routine **April 17, 10:15

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Every spring, the German human genetics community meets at the annual meeting of the GfH for three days packed with interesting lectures, workshops and discussions on the latest developments and news in clinical genetics.

Join team varvis® and team Nostos to learn about what’s new and what’s next in the varvis® software, incl. long-read whole genome sequencing, now also available for ONT data and the integration of AI-powered variant interpretation by AION.

Where can you find us? Booth #16.**Subscribe to our newsletter to make sure to get the latest updates and news on our events planning and not to miss out on our workshops, symposia and satellites.**

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