Webinar

Advancing Rare Disease Research with 10x Genomics

Register to watch on-demand
Advancing Rare Disease Research with 10x Genomics

The study of rare diseases presents unique challenges due to their low prevalence and often complex genetic underpinnings. Join us for a special webinar dedicated to exploring how 10x Genomics is transforming rare disease research through cutting-edge single-cell and spatial genomic technologies.

In this webinar, we will discuss the critical importance of advanced genomic solutions in unraveling the mysteries of rare diseases.

Key topics will include:

• The role of single-cell genomics in dissecting the cellular diversity and molecular pathways involved in rare diseases
• Real-world case studies illustrating the application of 10x Genomics technology in rare disease research, highlighting breakthroughs in diagnosis and treatment strategies
• Advances in spatial genomics that offer a comprehensive view of tissue architecture and cellular interactions, essential for understanding disease progression

Whether you are a researcher, clinician, or student, this webinar will provide valuable knowledge and tools to accelerate your rare disease research efforts. Participate in interactive Q&A sessions and engage with our panel of experts to gain deeper insights and foster collaborative opportunities.

Don't miss this opportunity to learn how 10x Genomics is empowering the rare disease research community to make significant strides towards improving patient outcomes and finding cures.

Date and Time: May 13, 2025 - 3pm CET

Join us for an informative and inspiring session that promises to shed light on the future of rare disease research with 10x Genomics.

Speakers

Koen de Gelas

Sr. Science & Technology Advisor
10x Genomics