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ASHG 2019

October 15–19, 2019 | American Society of Human Genetics, Houston, TX


Power a new future in molecular genomics.

Nanoscale reactions. Automated workflows. Real savings.

Learn how microfluidics-based genomics solutions can help you transform your laboratory productivity with walkaway automation delivering significant cost and operational savings.

Visit Fluidigm at Booth 1107


New! Introducing the Advanta RNA-Seq NGS Library Prep Kit

The Advanta™ RNA-Seq NGS Library Prep Kit empowers you to confidently generate high-quality stranded RNA-seq libraries using a streamlined Juno™ workflow. Ask us how you can minimize total hands-on time to approximately 2 hours while reducing library prep costs by up to 50%. Learn more at fluidigm.com/advanta-rnaseq.


Attend our Exhibitor Education Events

Our luncheon and breakfast workshops both take place at the Hilton Americas-Houston, Room 335ABC, located across the skybridge from the Convention Center.

Workshop 1: Redefining Library Prep for RNA-Seq Applications–A Microfluidics-Based Approach for Superior Workflow Efficiencies



Wednesday, October 16, 2019 | 12:45–2:00 pm
Hilton Americas-Houston, Room 335ABC
Gourmet box lunches will be served.*

Luncheon speakers


Scott Magness, PhD

Associate Professor, University of North Carolina School of Medicine
UNC/NCSU Joint Departments of Biomedical Engineering, Departments of Cell & Molecular Physiology, and Medicine
Director, Advanced Analytics Core, Center for Gastrointestinal Biology and Disease
Hypoxia-on-a-chip: Investigating transcriptomic changes at the micro-scale using RNA-seq



David King, PhD

Vice President, Research and Development, Genomics
Fluidigm
Development of an automated and cost-effective workflow for RNA-seq using Fluidigm microfluidic technology: the Advanta RNA-Seq system


Summary

RNA sequencing (RNA-seq) by next-generation sequencing (NGS) accelerates transcriptome studies by providing a sensitive and accurate hypothesis-free method to measure expression. Automation of nanoliter-scale library prep has the potential to significantly advance transcriptomics with streamlined methods to study complex events while substantially reducing associated costs.

In this workshop, speakers will discuss the application of RNA-seq using automated microfluidics-based library prep solutions.



Workshop 2: Moving Beyond Classification of Single Cells in Complex Systems Leveraging Microfluidics


Thursday, October 17, 2019 | 7:15–8:45 am
Hilton Americas-Houston, Room 335ABC American continental breakfast buffet will be served.*

Breakfast speaker


Jason McKinney
Director, Single Cell Genomics
Fluidigm

Summary

The evolution of single-cell genomic analysis has reached an inflection point where the information obtained from any given cell requires a preparatory technology that allows for deeper and wider interrogation. Come learn about our new total RNA-seq approach for automated NGS library prep of single cells using an integrated fluidic circuit (IFC), enabling full-length transcript analysis of both poly(A) and non-poly(A) genes while also retaining strand orientation. Additional applications that will be presented include CORTAD-seq (full-length mRNA and targeted genomic DNA from the same cell) and REAP-seq (mRNA and protein expression from the same cell), both of which represent exciting advances supporting multi-omic analysis of single cells.

*Meals offered while supplies last.

View and discuss Fluidigm posters with the authors

Friday, October 18, 2019 | 2:00–3:00 pm
Exhibit Hall, Level 1

Poster Number

Title

Presenting Author

Category

1754F Two NGS library prep panels for analyzing tumor cells for actionable mutations using a flexible, automated microfluidics platform. Tom Goralski Molecular Phenotyping and Omics Technologies
1874F Integration of molecular chemistries supporting a full-length, mRNA sequencing library preparation method on a microfluidic circuit Michael L. Phelan Molecular Phenotyping and Omics Technologies


Featured solutions on exhibit

Visit the Fluidigm booth to explore products up close and visit with us about your projects.

NEW! Advanta RNA-Seq NGS Library Prep Kit


The Advanta™ RNA-Seq NGS Library Prep Kit empowers you to confidently generate high-quality stranded RNA-seq libraries using a streamlined Juno™ workflow. Ask us how you can minimize total hands-on time to approximately 2 hours while reducing library prep costs by up to 50%. Learn more at fluidigm.com/advanta-rnaseq.

Juno Family

Juno™

Increase productivity and efficiency with automated, cost-effective and easy-to-use workflows for targeted DNA next-generation sequencing (NGS) library preparation.


Juno Family

C1™

Characterize selected cell populations with high molecular detection sensitivity using a broad menu of multi-omic single-cell assays.


C1


Contact us to learn more about the Advanta RNA-Seq NGS Library Prep Kit. Provide us with your contact information below.



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Fluidigm Products are for Research Use Only. Not for use in diagnostic procedures.