DNASTAR offers free, online webinars led by our own scientific and technical experts as another resource for helping you get the most out of our software. Register for one of the scheduled webinars below, or request a topic for a future webinar.
"Ryan's webinar was really helpful; I've been using the Lasergene Core Suite for years, but still learnt a few new things from the webinar."
Presented by: Matthew Keyser April 30th, 2014 at 12:00 pm EDT
In this webinar, DNASTAR's Matthew Keyser will demonstrate how to load miRNA data for miRNA discovery and quantification. Additionally, learn how to quanitfy miRNA sequence data against known miRNA templates.
Presented by: Jacqueline Carville Originally Aired: February 26, 2014
In this webinar, DNASTAR's Jacqueline Carville will demonstrate how to create and submit protein structure predictions using the NovaFold application. Learn how to analyze prediction results, as well as perform a variety of other protein analysis workflows such as epitope prediction, structural alignment, and motion visualization.
Presented by: Jacqueline Carville Originally Aired: January 29, 2014
In this webinar, we will use DNASTAR's Lasergene Genomics Suite software to analyze exome sequencing data from the breakthrough work of Ng et. al. (Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome. Nat. Genet. 42, 30-35 (2010)). This case study confirms the discovery of mutations in the MLL2 gene as a cause of the rare autosomal dominant Kabuki syndrome. Through this case study, we will give a live demonstration of the capabilities of Lasergene Genomics Suite as applicable to similar association studies.
Presented by: Jacqueline Carville Originally Aired: December 11, 2013
In this webinar, DNASTAR's Jacqueline Carville walks you through our various suites, applications, and support options. This overview introduces you to all DNASTAR has to offer, and cover topics in the realms of molecular biology, next-gen sequence analysis, and structural biology.
Presented by: Venkatesh Balakrishnan Originally Aired: November 20, 2013
In this webinar, DNASTAR's Venkatesh Balakrishnan demonstrates a de novo transcriptome workflow. Learn how RNA-Seq data is assembled in DNASTAR's SeqMan NGen application and visualized in SeqMan Pro. Gene expression analysis is then performed in the ArrayStar application.
Presented by: Jacqueline Carville Originally Aired: October 2, 2013
In this webinar, DNASTAR's Jacqueline Carville will showcase DNASTAR's newest application MegAlign Pro while giving a live demonstration of various sequence alignment workflows. Learn about the different alignment methods available in MegAlign Pro, as well as various downstream phylogenetic analysis capabilities.
Presented by: Matthew Keyser Originally Aired: August 28, 2013
In this webinar, DNASTAR's Matt Keyser will showcase the advanced SNP analysis capabilities of the Lasergene Genomics Suite. Learn how integrate SNP database information into large-scale, multi-sample SNP projects.
Presented by: Brian Anderson Originally Aired: August 14, 2013
In this webinar, DNASTAR's Brian Anderson demonstrates several virtual cloning and primer design workflows. Learn how DNASTAR supports all major virtual cloning techniques, as well as offers a variety of options for primer and probe design.
Presented by: Matthew Keyser Originally Aired: March 12, 2013
See Matt demonstrate several workflows in support of Illumina sequence assembly and analysis in Lasergene Genomics Suite. Topics covered include multiple exome comparisons, RNA-Seq analysis, automated bacterial genome closure, and de novo genome assembly on BaseSpace.
Presented by: Matthew Keyser Originally Aired: January 30, 2013
Matt shows you how to close gaps in your de novo and reference guided genome assemblies in Lasergene Genomics Suite. To learn more about the steps leading up to the gap closure process, please see our Automated Bacterial Genome Closure and De Novo Genome Assembly webinars below.
Presented by: Matthew Keyser Originally Aired: December 5, 2012
See Matt assemble a novel strain of bacteria using a closely related reference sequence as a template. The webinar includes a demonstration of how to select an appropriate referenc, align against that template and automatically resolve the majority of structural variations and gaps using Lasergene Genomics Suite.
Presented by: Amanda Mitchell Originally Aired: November 14, 2012
Hear Amanda discuss the proteomics tools available in Lasergene 10.1 as she demonstrates some of the most powerful features in Protean 3D, including: epitope prediction, structural alignment, and macromolecular motion visualization.
Presented by: Katie Maxfield Originally Aired: September 24, 2012
See what's new in our latest release, including automated genome assembly with gap closure, RNA-Seq analysis, large scale variant analysis, epitope prediction, structural alignment, and advanced sequence editing.
Presented by: Ryan Jacob Originally Aired: June 13, 2012
Hear Ryan discuss some of the most powerful functions of Lasergene Core Suite, including sequence editing, plasmid map creation, virtual automated cloning, SNP reporting, sequence alignments, gene finding, and primer design.