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Genomic Variant Analysis & Clinical Interpretation is a 16 module online course providing hands-on exposure to analysis and clinical interpretation of genomic variants.
The GVACI 2022 Course has started. Please login to the Learning Portal to access the course. No emails would be sent.
Special Registration for Students
Registrations are open until November 30th, 2022 for undergraduate and postgraduate students in life sciences
If you do not have a GVACI portal login yet, please re-register yourself using the link, even if you have registered previouslyThe GVACI 2022
The GVACI 2022
Course
Course
IN NUMBERS
2000+
2000+
Registrants
40+
40+
Countries represented
16
16
Learning Modules
10+
10+
Faculty
Course Overview
Course Overview
While genomics is increasingly being applied in clinical settings for diagnosis, prognosis and precise management of diseases, there is a dearth of expertise and knowledgebase to adequately interpret evidence on genetic variants to impact healthcare decisions.
This course provides an overview of the concepts and methods of genomic variant analysis and clinical interpretation.
Faculty
Faculty
Anjali Bajaj
Vishu Gupta
Abhinav Jain
Bani Jolly
Who can attend ?
Who can attend ?
Clinicians, Clinical Geneticists and Genetic Counsellors, Undergraduate and postgraduate Medical Students, Nurses and Nursing Students. Faculty members in medical teaching and research organizations
What will I learn ?
What will I learn ?
You are expected to learn about the basic concepts of genetics and genomics, variant nomenclature and tools for variant analysis as well as their clinical interpretation. The course would follow the Standards and guidelines for the interpretation of sequence variants as per the joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Association for Molecular Pathology (AMP). Individuals who clear the course are expected to be well versed with the basic concepts of genomics as well as approaches to independently evaluate evidence and interpret the pathogenicity of genetic variants.
Genomics of Rare Diseases in India
Genomics of Rare Diseases in India
Genomics for Understanding Rare Diseases India Alliance Network (GUaRDIAN) is a consortium of over 300 clinicians and researchers from over 70 medical and research centers making it one of the largest clinical genomics research networks in India for Rare Genetic Diseases.
The programme is funded by CSIR India. Learn more
Read more about the programme in the recent overview Genomics of rare genetic diseases—experiences from India Human Genomics 13:52 (2019)
This educational initiative has been organised as part of the educational outreach of GUaRDIAN.
The CSIR-IGIB Sanofi Genzyme Fellowship in Genomics for Medical Professionals aims to introduce fundamental aspects of genomics and molecular medicine to clinicians through short-term visit, interaction and hands-on training on specific aspects of genomics with the faculty at the CSIR-Institute of Genomics and Integrative Biology (CSIR-IGIB) in Delhi.
This fellowship programme was made possible with an unrestricted educational grant from Sanofi Genzyme. The funders have no role in the creation of content, selection of participants or administration of the course.
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