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Webinar

Part 2: Decoding long-reads with powerful bioinformatics tools

On-demand
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May 28, 2025
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60 minutes
Oncology
Cancer (other / various)
Next Generation Sequencing

About this webinar

Building on the foundational knowledge from part one, this session focuses on the critical aspects of secondary analysis for long-read panel data. 

We’ll guide you through essential considerations for constructing high-performing bioinformatics workflows, including tailored read alignment strategies optimized for long reads, advanced variant calling algorithms to detect structural variations and tools for accurate haplotype phasing and visualization. 

Discover how to refine your pipeline to improve the accuracy and interpretability of your long-read data. Explore best practices for downstream analysis – empowering you to extract meaningful insights and apply them confidently in both research and diagnostic settings. 

By the end of this session, you’ll have a clear roadmap for leveraging the full potential of long-read panels in your genomic studies.

Speakers