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In this video, we dive into the world of DNA and DNA sequencing technologies, explaining paired vs single-end reads, and covering the key sequencing technologies: Sanger sequencing, Illumina short reads, Nanopore, and PacBio long reads.

Whether you’re just starting out in Bioinformatics or looking to deepen your understanding of sequencing technologies, this video will provide a clear breakdown of the technologies driving genomics research today.

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What You’ll Learn:
• What DNA is and how it forms the basis of life
• The difference between paired-end and single-end reads
• Sanger sequencing: The first widely used sequencing method
• Illumina sequencing: High-throughput short reads for large-scale data
• Nanopore sequencing: Real-time long reads with high flexibility
• PacBio sequencing: High accuracy long reads for complex genomes
• The pros and cons of each sequencing method and their applications in genomics and Bioinformatics

By the end of this video, you’ll have a strong understanding of DNA sequencing technologies and how they’re used in genomic analysis, research, and clinical applications.

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Perfect For:
• Bioinformatics learners
• Genomics students
• Researchers working with sequencing data
• Data Scientists interested in DNA sequencing technologies
• Students looking to understand the latest in sequencing technology



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Here is the complete roadmap to become a data scientist, data analyst and machine learning engineer in next 4-8 months (depending on your pace)
All lectures are free of cost, just need your prayers.
Here is the link to the course: www.codanics.com/roadmap
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