Welcome to GENEYX COURSES
Guided Training from Geneyx Experts
Get access to real cases that highlight the scientific principles and tools that are crucial for genomic analysis and interpretation in the context of clinical practice.
STUDENTS:
This course is designed for health professionals working in diverse domains; clinical professionals (consultants and trainees) and clinical scientists who require knowledge and hands-on training in the Principles of Variant Interpretation and an in-depth understanding of American College of Medical Genetics variant interpretation guidelines.
Please note: Previous knowledge is mandatory of the following modules: Basic genetics, Population genetics, and Genetic work-up methodologies.
WHEN: (2-month course) Starting 5 March 2024 – 30 April 2024
Every Tuesday at 8:30am – 10:30am (Pacific Time)
AIM: Provide attendees with the necessary skills for navigating the rapidly evolving landscape of genomic & personalized medicine.
ONLINE: The online sessions will feature active engagement
EXPERTS: Conducted by experts in their fields, Hagar Mor-Shaked and Ali Tabish.
ACCESS TO GENEYX ANALYSIS: In addition, each participant will be provided access to the Geneyx platform for training purposes.
CERTIFICATION: Upon completion of the course, participants will be awarded certification.
Scientific sessions
- *Tools for variant interpretation
- *Single nucleotide variant (SNV) and copy number variant analysis (CNV)
- *The ACMG guidelines and interpretation for SNV and CNV
- *Case studies
- *A protein view of variants
- *Exome sequencing analysis
- *Whole genomes sequencing analysis
HOW TO APPLY:
Click here to register for the course.
After registering, you will receive a confirmation email containing information about joining.
Spaces are limited. Good Luck!
PROGRAM AT A GLANCE:
Date | Class number | Topic | Presenter |
03/05/2024 | 1 | Introduction to NGS, Bioinformatic pipelines | Hagar |
03/05/2024 | 2 | Introduction to Variant interpretation, tools, and databases (ClinVar, gnomAD, Decipher, etc.) | Hagar |
03/12/2024 | 3 | Variant interpretation, cases from the clinic | Hagar |
03/19/2024 | 4 | ACMG/AMP guideline for single nucleotide variant interpretation, ClinGen guidelines – part I | Ali
|
03/26/2024 | 5 | ACMG/AMP guideline for single nucleotide variant interpretation, ClinGen guidelines – part II | Ali
|
04/02/2024 | 6 | Structural variants, copy number variants, tools, and databases (DGV, gnomAD-SV, etc.) | Ali
|
04/09/2024 | 7 | ACMG/AMP guideline for copy number variant interpretation | Ali
|
04/16/2024 | 8 | Solving cases together, part I (exomes and genomes) | Ali |
04/23/2024 | 9 | Solving cases together, part II (Long reads sequencing) | Hagar |
04/30/2024 | 10 | Future directions in clinical genomics and course summary | Hagar |
