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Finding the critical Genetic Needle in a 6 billion Genome Haystack
March 9, 2022 - 2PM CET (KSA: 4PM – UAE: 5PM)
The greater part of human physical features is coded and stored in the genomes. This also includes congenital and later onset defects. By examining an individual’s genome, genetic conditions can be identified that can help manage a clinical condition.
During this Webinar, our Sr. Director Bioinformatics Research, Dr. Najim Ameziane, a molecular biologist with 15+ years of experience in molecular diagnostics of hereditary disease, will help you understand the following:
- How an individual’s genome is “analyzed”?
- How to identify the relevant genetic variant within an individual?
- How to identify the genetic mutations?
- How do the different types of genetic mutations that can cause different diseases?
Najim holds a PhD in human genetics with over 15 years of experience in molecular diagnostics of hereditary disease and cancer. He pioneered the application of next-generation sequencing in the clinical genetics department of the VU Medical Center Amsterdam. He discovered novel gene-disease associations by utilizing cutting-edge technologies in the laboratory as well as bioinformatically. Najim is passionate about deciphering the human genome, which holds the code of life. He believes that comprehension of the human genome is key towards personalized management of genetic disease and improved quality of life.
Speaker
Dr. Najim Ameziane,
Sr. Director Bioinformatics Research Arcensus GmbH
Najim holds a PhD in human genetics with over 15 years of experience in molecular diagnostics of hereditary disease and cancer. He pioneered the application of next-generation sequencing in the clinical genetics department of the VU Medical Center Amsterdam. He discovered novel gene-disease associations by utilizing cutting-edge technologies in the laboratory as well as bioinformatically. Najim is passionate about deciphering the human genome, which holds the code of life. He believes that comprehension of the human genome is key towards personalized management of genetic disease and improved quality of life.
Speaker
Dr. Najim Ameziane,
Sr. Director Bioinformatics Research Arcensus GmbH
Finding the critical Genetic Needle in a
6 billion Genome Haystack
March 9, 2022 - 2PM CET
2022. All rights reserved by Arcensus GmbH
2022. All rights reserved by Arcensus GmbH
IThe greater part of human physical features is coded and stored in the genomes. This also includes congenital and later onset defects. By examining an individual’s genome, genetic conditions can be identified that can help manage a clinical condition.
During this Webinar, our Sr. Director Bioinformatics Research, Dr. Najim Ameziane, a molecular biologist with 15+ years of experience in molecular diagnostics of hereditary disease, will help you understand the following:
- How an individual’s genome is “analyzed”?
- How to identify the relevant genetic variant within an individual?
- How to identify the genetic mutations?
- How do the different types of genetic mutations that can cause different diseases?
Duration: 45 minutes
(KSA: 4PM – UAE: 5PM) - Duration: 45 minutes
It takes only a single nucleotide alteration out of 6 billion to cause a severe genetic disease
Some genetic diseases are inherited while others occur de novo
Comprehensive variant detection analysis, including all variant types, is critical to reach the highest diagnostic yield
Key Messages: