Lasergene Genomic Tools for Common Next Generation Sequencing Workflows

As the availability of NGS technology has increased, so have the tools for genomic data analysis. However, NGS data analysis often remains a challenge due to the sheer volume of data, the computing power needed, and the technical expertise required to prepare a project for assembly and analysis. 

Lasergene Genomics stands apart in the field of genomic data analysis due in part to SeqMan NGen, our revolutionary tool that enables you to run your project in mere minutes.  The session will introduce the Genomic Suite tools and walk you through some common WGS and RNASeq next gen sequencing workflows.  

Workshop Agenda

•    Downloading Short Read Archive NGS sequencing data
•     Working with FastQC for NGS data quality reporting  
•     RNASeq Analysis with PCA, Volcano, MA Plots, etc.
•     WGS with variant annotation (GATK Haplotype, Mutect2 (GERMQ, MMW, POPAF, etc)
•     Augustus/SwissProt annotation  

This workshop will be taught by a Scientist from DNASTAR. The session is designed for new users, or experienced users, or anyone interested in expanding their understanding of DNASTAR’s capabilities across molecular biology, genomics, and structural biology.