Description

This course is DNA and RNA Sequencing:

The workshop begins with an overview of sequencing technologies, including Sanger sequencing, next-generation sequencing (NGS), and emerging single-molecule sequencing techniques. Participants will gain insights into the principles behind each technology, their applications in various fields such as genomics, transcriptomics, and personalized medicine, and the advantages and limitations of different sequencing platforms.
Hands-on sessions will provide practical experience in DNA and RNA sample preparation, library construction, sequencing library QC, and setting up sequencing runs. Participants will learn best practices for data analysis, including base calling, sequence alignment, variant calling, and interpretation of sequencing results.
Led by expert instructors with extensive experience in genomics and sequencing technologies, this workshop combines theoretical knowledge with practical demonstrations and interactive exercises. Participants will also explore bioinformatics tools and pipelines used for processing and analyzing sequencing data, gaining proficiency in interpreting genomic and transcriptomic information.
A key focus of the workshop will be on understanding the applications of DNA and RNA sequencing in research and clinical settings, such as identifying genetic variations, studying gene expression profiles, investigating microbial diversity, and advancing personalized medicine initiatives.
Whether you are new to sequencing technologies or seeking to expand your expertise, this workshop offers a comprehensive foundation for leveraging DNA and RNA sequencing in scientific research and applications. Join us to advance your skills, explore the forefront of genomic technologies, and unlock new opportunities in genetics and biotechnology. Register now to secure your place and embark on a transformative journey in DNA and RNA sequencing!