About this event
NGS is over 20 years old, yet it is harder than ever to navigate the market. With new players and new chemistries, researchers now have a powerful arsenal of tools available to them, but understanding these tools is challenging, let alone knowing how to pick between them.
This webinar series – Sequencing: A State of Play – addresses these challenges head on. If you have questions about sequencing or are looking for tips, tricks and lessons learned for the latest sequencing methods, you won’t want to miss this one.
This webinar series will provide you with:
Thursday 26th September at 3pm BST / 4pm CET / 10am EST
Get ready for the ultimate debate of when to use long or short read sequencing. Webinar 3 brings together three experienced long-read and short-read adopters as they cover the long-read/short-read debate. Will long-read replace short-read? Bring your questions to webinar 3 to find out what the experts think.
Speakers:
Miten Jain, Associate Professor, Northwestern University
Elsa Molina, Director, Next Generation Sequencing & Genomics Core, Salk Institut
Sara Goodwin, Research Assistant Professor, Cold Spring Harbor Laboratory
By the end you will leave with:
Now available on demand
Webinar 1 eases you into the series by getting back to some of the basics. This webinar is an excellent opportunity to hear about the fundamentals of sequencing, get a review of the different chemistries, and to learn about the considerations for choosing between them.
Speakers:
Talk 1: An Introduction to Sequencing
Niall Lennon, Senior Director, Genomics Platform, Broad Institute
Talk 2: Considering Platform Choice For Sequencing Experiments
Claire Bailey Hartmann, Director of Bauer Core Facilities, Harvard University
By the end you will leave with:
Now available on demand
Webinar 2 gets into the nitty gritty of sequencing and is rich in tips and tricks from three sequencing professionals. How do you get the most out of your samples and generate the best quality data downstream? Webinar 2 has your answers.
Speakers:
Talk 1: Sequencing Success - Expert Tips and Techniques
Elsa Molina, Director, Next Generation Sequencing & Genomics Core, Salk Institut
Talk 2: From Sample to Sequencing Success - How To Deal With Difficult Samples
Sally James, Head of Genomics, University of York
Talk 3: Lessons Learned from Early Adoption of New Short-Read Sequencers
Michael Peterson, Scientist I, Stowers Institute for Medical Research
By the end you will leave with:
Hosted by
I am an Assistant Professor in the department of Bioengineering and department of Physics at Northeastern University, Boston. My research interests include genomics, computational biology, machine learning, big data, mobile apps, nanopore technology, DNA, RNA and protein sequencing, long reads, de novo assembly, nucleotide modifications, epigenetics, solving complex biological questions Specialties: Bioinformatics, genomics and computational biology, nanopore technology, MinION, molecular and cell biology, analytical instrumentation, recombinant DNA technology, protein chemistry, microbiology, nanotechnology, metal (gold, silver, and iron) nanoparticles, liposomes.
Front Line Genomics is a genomics-focused media company, with a social mission to deliver the benefits of genomics to patients faster. We organise the Festival of Genomics, digital events and webinars. We also produce reports and operate a content-rich website.