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Various dates throughout May & June

Hear from clinical genomic leaders as they present variant interpretation best practices through case studies and real-life validations across a variety of applications that aided in the improvement of their laboratory output.

Watch the session most relevant to you or attend all five. 

An unorthodox journey and our experience for validation of NxClinical and the GSA Beadchip microarray

dale wright
Dale Wright, Head of Cytogenetics for Sydney Genome Diagnostics at The Children’s Hospital at Westmead, Sydney

Watch here


Significance Associated with Phenotype (SAP) Score: A Method for Ranking Genes and Genomic Regions Based on Patient’s Phenotype

Jenny Ji with border

Jianling Ji, MD, MS, FACMG, Assistant Director of Clinical Genomics Laboratory, Center for Personalized Medicine, Assistant Professor of Clinical Pathology, Keck School of Medicine of USC

Watch here

Embracing the power of the SNP. NxClinical facilitates detection of UPD and determination of parent of origin from SNP microarray data.

Amber Boys with border
Amber Boys, Senior Medical Scientist in the Division of Genetics and Genomics at the Victorian Clinical Genetics Services, Melbourne

Watch here

Implementing high-throughput cloud-based microarray analysis in the UK Genomic Medicine service

dale wright (1)

Dom McMullan, Consultant Clinical Scientist at West Midlands Regional Genetics Laboratories (WMRGL), Birmingham and leads the Rare Disease and Reproductive Genomics Programme. Lead Scientist for Rare Disease Genomics for the Central and South Genomic Lab Hub

Watch here

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Real-world experience utilizing NxClinical for CNV detection using standard-of-care testing in Post-natal specimens

Colleen Bilancia, Ph.D. DABMGG, and Moises Serrano, Ph.D. ABMGG

Watch here