Introduction:

mRNA-seq is a powerful approach to study gene expression, alternative splicing, and genetic mutations. It also serves as a core component in multi-omics research, for example, integrating with epigenomics to reveal how DNA modifications regulate transcription, or with metabolomics to link gene expression changes to metabolic pathway activity and phenotypes.

Yet achieving reliable results involves more than just sequencing, careful planning at every step matters. In this webinar, we will walk you through the key considerations for successful mRNA-seq and show you how Novogene’s end-to-end solution, from RNA extraction and library preparation to bioinformatics and cloud-based support, helps you generate high quality, reproducible transcriptome data with confidence.

Learning Objectives:

• What is mRNA sequencing: A clear overview of the technology and its applications
• What parameters ensure success: RNA amount, RIN, biological replicates, and sequencing depth
• How does NovoMagic Plus help: Cloud-based platform for figure generation, differential expression analysis, and other advanced bioinformatics analysis

Discover how an integrated end-to-end approach can help generate high-quality transcriptomic insights for your research now. Speakers:

Liu Rui / Novogene AMEA Product Manager