Learn More About SOLiD® Next-Generation Sequencing and Applications
Next-generation sequencing projects require the best tools with the best support. And not all projects are the same, which is why we offer a broad portfolio of solutions and seamless workflows to deliver the high-quality sequencing data you expect. Experience industry-leading accuracy and pay-per-lane sequencing using the 5500 Series Genetic Analysis Systems. Choose best-in-class consumables optimally formulated for your platform and application. Complete your sequencing experiment with scalable, biologist-friendly data analysis using LifeScope™ Genomic Analysis Solutions. The webinars below are designed to introduce you to our products and the applications that they enable.
Register & Listen to Webinars
|Original Air Date||Abstract||View the Recorded Webinar|
|October 27, 2011||5500 Series Genetic Analyzers: Wildfire Technology Roadmap
Learn Wildfire technology and the promise it holds for simplifying the workflow and improving the throughput of the 5500 Series Genetic Analyzers.
|2011||LifeScope™ Software Training Series
Three sessions focused on LifeScope™ Software. Topics include:
|2011||5500 SOLiD™ System Training Series
NGS-226 -1 XSQ File Format and XSQ Tools (25 minutes)
|2010||SOLiD™ Success Stories in Cancer Research
The advent of ultrahigh-throughput sequencing has introduced new and boosted the capabilities of older methodologies. This training will demonstrate how the SOLiD™ System has been applied to cancer research by focusing on published cancer research using on the SOLiD™ System. The session will cover resequencing, targeted and whole genome sequencing transcriptome and miRNA analysis.
|2010||SOLiD™ de novo Training Series
Two sessions focused on de novo assembly of small genomes using the SOLiD™ System. Topics include:
|2010||SOLiD™ Epigenomics Training Series
Five sessions focused on SOLiD™ epigenomics. Topics include:
|2010||SOLiD™ Targeted ReSeq Training Series
Four sessions focused on the Targeted ReSeq application, covering the end-to-end workflow, from how to design a Targeted ReSeq experiment to performing data analysis. Topics include:
|2010||SOLiD™ RNA-Seq Training Series
"Nine sessions focused on the RNA-seq application, covering the end-to-end workflow from how to design an RNA-seq experiment up to how to perform data analysis. You will learn: what are the important questions you need to ask before defining which type of study to perform; tips & tricks to be successful during library prep; the power of barcoding; and how to perform data analysis using Life Technologies and third Party tools. Topics include:
Dr Rebecca J Leary from the Ludwig Center for Cancer Genetics and Therapeutics at Johns Hopkins Kimmel Cancer Center
|2010||Whole Cancer Genome Sequencing: Progress Toward Common Application
Dr Stanley F Nelson from the Department of Human Genetics at David Geffen School of Medicine at UCLA
|Genomics-Guided Therapeutic Options for Oncology: Is it Feasible?
Dr John Carpten from the Division of Integrated Cancer Genomics at TGen
|Breakthroughs in Mendelian Disease Research
Dr Alex Hoischen from Nijmegen
For Research Use Only. Not for use in diagnostic procedures.