詳細
Illumina next-generation sequencing (NGS) has been the most widely adopted technology for human whole-genome sequencing (WGS), delivering an accurate, scalable, cost-effective solution, featured in over 300,000 scientific publications. However, a small portion of the genome remains challenging to map due to highly repetitive or highly homologous regions. Illumina Complete Long-Reads will address these edge cases and accelerate access to the remaining ~5% of genic regions. In this presentation, we will share use cases of Complete Long Reads and highlight research being done by collaborators around the world.
Speakers:
Marwan Shinawi, MD, FACMG
Professor, Pediatrics Division of Genetics and Genomic Medicine
Washington University School of Medicine in St. Louis
David Silva
Staff Product Manager, Product Management
Illumina
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- 日時
- 2023/03/17
- 11:20 AM
- Location
- North America
- Affiliation
- Illumina
- Presenter
- David Silva
- Topic
- Genetic & Rare Diseases