Accurate Variant Detection from Long-Read Sequencing
Автор: SoftGenetics
Загружено: 2025-07-30
Просмотров: 72
An Introduction to NextGENeLR
Long-read sequencing platforms like PacBio and Oxford Nanopore open new possibilities for variant analysis, but they also introduce higher error rates and complex interpretation challenges.
This free webinar addresses these challenges using NextGENeLR, a new analysis software from SoftGenetics.
In this session, Kevin Levan from SoftGenetics covers:
Reducing false positives in SMV and indel detection
Identifying large deletions, insertions, and translocations - Haplotyping across SNPs, indels, and structural variants
STR detection for diseases like Huntington’s and Fragile X
Real-world case studies in prenatal testing, CRISPR analysis, and COVID-19 sequencing
Whether you're a researcher, clinician, or bioinformatics enthusiast, this webinar will guide you through the key features, practical use cases, and unique advantages of NextGENeLR in modern genomics.
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