Event – ESHG 2019 | Booth 446 2019-06-05T12:23:55+00:00

ESHG 2019 Meeting | Booth 446
June 15 – 18, 2019
Gothenburg, Sweden 

Join us for the following Events at ESHG:

CleanPlex® Technology for MGISEQ NGS Platform

Presentation | CleanPlex for MGI: A Targeted NGS Solution with Exceptional Coverage Uniformity and Rapid Customization
Speaker | Edward Jan, PhD, Director of Product Marketing, Paragon Genomics Inc., USA

CleanPlex Ready-to-Use and Custom NGS panels are now available for sequencing analysis on the MGISEQ platforms. In this presentation Dr. Jan will describe the technology, workflow and how you can achieve superior results using CleanPlex for MGI products.

Saturday, June 15, 2019  | 10:00 to 11:30 am
Room A-3 Svenska Mässan Gothia Towers

Corporate Satellite Meeting: Towards a Perfect Genome
Sponsored by MGI − a subsidiary of BGI Group

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Learn how CleanPlex® Custom NGS Panels can be combined with SOPHiA™ Platform for rapid genomic analysis of hereditary diseases

Presentation | Molecular profiling of osteogenesis imperfect through a targeted gene panel powered by SOPHiA
Speaker | Sehime Gülsün Temel, MD, PhD, Assoc. Prof., Department of Medical Genetics, Uludag University Hospital, Turkey

Osteogenesis Imperfecta (OI) is characterized by bone fragility and consequent susceptibility to bone fractures. In this presentation, Prof. Temel will describe the use of a CleanPlex custom NGS panel containing 14 genes implicated for OI, in combination with the SOPHiA’s genomic analysis platform, to rapidly and accurately identify pathogenic variants.

Sunday, June 16, 2019  | 3:00 to 4:30 pm
Room A-1 Svenska Mässan Gothia Towers

Corporate Satellite Meeting: Hereditary disorders solutions powered by SOPHiA: Overcoming Challenges to Increase Diagnostic Yield
Sponsored by SOPHiA GENETICS

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Poster Sessions

Monday, June 17, 2019

P15.17D | Determining genetic predispositions using CleanPlex Hereditary Cancer Panel for a rapid and streamlined amplicon-based NGS workflow

P12.150C | Ultra-high multiplexed 20,000-amplicon NGS panel for tumor mutational burden (TMB) analysis using a rapid 4-hour workflow

P16.75C | An ultrafast amplicon-based targeted library preparation method using double-stranded unique molecular identifiers for detecting rare mutations in cell-free DNA
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Booth #446 | Svenska Mässan Gothia Towers

Stop by our booth to meet our team and learn how you can discover more with less™ using CleanPlex NGS Panels. 

CleanPlex Hereditary Cancer Panels – multiplex PCR-based targeted sequencing, a cost-effective method to assess heritable cancer risk.

ParagonDesigner™ Portal – simplifies building of custom NGS assays via a web-based tool

See you in Gothenburg!

Contact us to schedule a time to meet and discuss your project needs.