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Attending the upcoming European Society of Human Genetics (ESHG) virtual conference? Please join us for this live Corporate Satellite Meeting:



“Time to change: Transitioning from arrays to NGS in CLL & ID/DD analysis with confidence”

Monday, August 30th, 15.30 – 16.30 CEST

In this session you will discover how two scientists have streamlined their laboratory workflow using OGT’s next generation sequencing (NGS) panels, allowing them to accurately detect a wide variety of genetic aberrations.

Our speakers:

Elizabeth McCready, PhD, FCCMG
Hamilton Regional Laboratory Medicine Program; Associate Professor, McMaster University

"Clinical evaluation of an NGS-based assay for the detection of CNV and SNV acting synergistically to affect phenotype."

Fléchère Fortin, PhD, FCCMG
Scientific Director, Cytogenetics laboratory, Medical Genetics Division, CIUSSS de l’Estrie-CHUS                                                                                                                                 

"Genetic evaluation of CLL: transitioning from a SNP-array CGH platform to an NGS-based CNV+SNV approach."