12th Annual Next Generation Sequencing & Clinical Diagnostics Congress04 - 06 November 2020, GMT (UTC+0)

An outstanding and comprehensive programme discussing key areas shaping next generation sequencing, drug development and personalised healthcare. Case studies include integration of NGS to clinical development to personalised therapies and innovative treatments.

Last Year's Event Included...

Over 1000 attendees representing internationally renowned academic institutions, research institutes and hospitals as well as global pharmaceutical organisations and leading biotech companies.

Over 80 case studies, presentations, panel discussions focused on the key issues in microbiome research, multi omics data integration, delivering genome-based medicine, spatial transcriptomics, single cell analysis emerging trends and single cell analysis in drug research & development.

PLUS interactive opportunities including:

  • Panel Discussions
  • Pre-Event Webinars
  • Pre-Event Speaker Q&As and Spotlights

Agenda at a Glance

Pre-Event Deep Dive Sessions

  • Microbiome Methodologies
  • Single Cell Proteomics
  • Clinical Diagnostics & Precision Medicine Multi-Technology Session

Day One

  • Delivering Genomic-Based Medicine
  • Multi Omics Data Integration & NGS Informatics

Day Two

  • Part 1 – Long & Short Read Sequencing
  • Part 2 – Data Analysis & Management

Investigating Human Health And Disease At Single-Cell Resolution

Pre-Event Focus Day Workshop from our Diamond Sponsor.
03 November 2020 | 14:00 – 17:00 GMT

This complimentary workshop is bringing together a panel of worldwide experts in single genomics to discuss how human health and disease can be resolved at the single-cell level. 

Workshop chaired by: MATTHIEU PESANT, PhD, Product Manager NGS, Takara Bio, France