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Illumina TruSight® HLA Workshop - San Diego

Achieve unambiguous HLA typing results using a single assay

On behalf of the Illumina HLA team, we invite you to join us for an engaging 3-day, hands-on workshop to explore how next-generation sequencing (NGS) is delivering accuracy and efficiency to HLA typing. Discover why the TruSight® HLA Sequencing Panel has the potential to become a new paradigm in HLA typing.

During this this free educational workshop you will have the opportunity to network with your peers and learn about Illumina’s ultra-high resolution DNA-to-report solution, with the TruSight® HLA Sequencing Panel. The workshop also includes presentations on automating the NGS workflow, and ASHI accreditation submission. 

Ground transportation and meals will be provided.

New in 2017
We will be offering an optional introductory session on NGS.  The Basics of NGS seminar is designed to help laboratory scientists gain proficiency in the essential aspects of NGS.  The seminar will cover TruSight® HLA library preparation, cluster generation, advances in sequencing technology, Illumina sequencing chemistry and systems, and feature live demos of Illumina benchtop sequencing systems.  If you are interested in attending this session please select the NGS 101 program during registration.  Participants will receive additional continuing education credits for attending.

 

This is an official continuing education program approved by the American Board of Histocompatibility and Immunogenetics (ABHI). Attendees are eligible to receive 2.85 ABHI continuing education credit (CEC). There is no charge to attend this event but registration is required

Register now as space is limited.

San Diego, CA | North America
Topic: Human Genetics & Genetic Disease : HLA Typing
2017 Illumina User Group Meeting - Mid Atlantic

Join us for an exciting day at the Hilton Washington DC/Rockville Hotel & Executive Meeting Center, May 4, 2017.

The Illumina User Group Meeting is a great opportunity for you to learn more about advancements in genomics, discuss protocol optimization and hear about bioinformatics solutions.

This year, we will be featuring many interactive sessions and new program enhancements:

  • Application reviews featuring the latest technologies from new sample preparations to data analysis tools, for applications like single cell sequencing, immuno-oncology, metagenomics, epigenetics and much more
  • Product updates in sequencing and arrays, including the recently introduced NovaSeq™, and highlighting how researchers are combining array-based DNA Methylation with RNA-Seq to better characterize human disease
  • Multi-omics panel discussion approaches focusing on the integration of quantitative, qualitative, and genomic data
  • One-on-one appointment scheduling and a mobile event application for the meeting

Who Should Attend:
Illumina User Group Meetings are exclusively for those who own, use, or have their data generated on Illumina instrumentation. The presentations will cover a broad range of applications, and are designed for new or experienced users in the areas of optimization of the sequencing workflow or bioinformatics.


 

Rockville, MD | North America
Topic: Cancer Genomics : Human Genetics & Genetic Disease : Microbiology & Infectious Disease