Maximizing Genomic Insights: An In-Depth Look at Long Read Sequencing
The advent of long read sequencing technology has revolutionized the field of genomics. It overcomes the limitations of short reads, enabling comprehensive analyses of complex genomic regions, including structural variations, genome phasing, and native nucleic acid sequences.
In this webinar, we will explore the principles behind PacBio SMRT and Oxford Nanopore technologies, how they differ from short read platforms and the way they improve assembly and variant calling quality and accuracy, reveal novel genes and isoforms, and enhance our understanding of microbial communities. By referencing published case studies, we will highlight the advantages and applications of long read sequencing, demonstrating how it answers complicated biological questions in genomics, transcriptomics, epigenomics and metagenomics.
Learning Objectives:- Introduction to Long Read Sequencing Technology: Understand the principles, strengths, and complexities of long read sequencing platforms.
- Advantages and Applications of Long Read Sequencing: Explore a variety of long read sequencing applications, and through the demonstration of practical examples, highlight how this technology can enhance your own research.
- Experimental Design, Sample Requirements and Data Analysis: Discuss key aspects of planning and executing long reads sequencing projects. Plus, learn about our End-to-End Services for long read sequencing projects here at Novogene Europe.
Whether you are new to long read sequencing or an experienced researcher, this webinar is designed to offer practical guidance and valuable insights. Don’t miss this chance to stay updated on the latest in long read sequencing and how Novogene Europe can facilitate your research endeavours.
