Registration Is Open
Expert-led course, Long Read Sequencing: Analysis, Annotation, and Interpretation, and gain hands-on experience with long-read sequencing (LRS) technology.
Whether you’re a researcher, geneticist, or bioinformatician, this four-week intensive program will equip you with the knowledge and skills to leverage LRS for advanced genomic insights.
📅 Dates: 22 April – 13 May 2025
⏳Duration: 4 weeks
🕒 Time: 14:00 London (GMT)
🎟 Limited seats available—secure your spot now.
Sign UP to Geneyx Analysis to complete the course homework in week 3:
A Step-By-Step Guide on how to open a Geneyx account
Schedule:
Week 1: Introduction to Long-Read Sequencing
Differences between Short-Read and Long-Read Sequencing
Overview of sequencing platforms
(Oxford Nanopore Technologies & PacBio)
Variant types and their impact
Real-world clinical case study
Week 2: Clinical Use Cases
The impact of LRS on rare disease diagnosis
Diagnostic uplift and phenotype-driven insights
Data-driven discussion using LRS publications
Week 3: LRS Data Analysis
Overview of secondary analysis options
LRS data annotation with key databases (Colors DB, etc.)
Introduction to Geneyx: Phasing and methylation analysis
Geneyx LRS Demo + hands-on homework with real LRS cases
Week 4: Clinical Adoption of LRS
The role of LRS in Rapid NICU sequencing
Pharmacogenomics (PGx) applications
Intraoperative brain tumor classification with LRS
Our Speakers
Engaging, expert-led online sessions that keep you head
and enhance your expertise!
Hagar Mor-Shaked PhD.
Senior Variant Scientist
Suzie Drury PhD.
Senior Variant Scientist
