BioDiscovery Webinars
Topic: Copy Number
Choose by Resource, then filter by Product OR Topic
Next-Generation Sequencing Assessment of HRD
This webinar is geared towards those involved with genomic variation analysis and interpretation of homologous recombination deficiency (HRD) from microarray data or next-generation sequencing (NGS) data in cytogenetics, molecular pathology, or molecular genetics labs.
Rapid implementation of the latest technical standards with the NxClinical integrated ACMG scoreboard
This webinar is geared towards those involved with genomic variation analysis and interpretation of copy number variation (CNV) from microarray data in cytogenetics or molecular genetics labs.
Copy Number Variant Detection by NGS: Coverage, Uniformity & Resolution
This webinar is geared towards those involved with genomic variation analysis and interpretation of copy number variation (CNV) from next-generation sequencing (NGS) data in cytogenetics or molecular genetics labs.
Genome sequencing reveals cause of multi-generational split hand/split foot with long bone deficiency
This webinar is geared towards those involved with genomic variation analysis and interpretation of microarray and sequencing data in cytogenetics or molecular genetics labs.
Real-world experience utilizing NxClinical for CNV detection using standard-of-care testing in Post-natal specimens
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
Implementing high-throughput cloud-based microarray analysis in the UK Genomic Medicine service
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
Embracing the power of the SNP. NxClinical facilitates detection of UPD and determination of parent of origin from SNP microarray data.
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
Significance Associated with Phenotype (SAP) Score: A Method for Ranking Genes and Genomic Regions Based on Patient’s Phenotype
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
An unorthodox journey and our experience for validation of NxClinical and the GSA Beadchip microarray
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
Increasing the yield of whole exome sequencing (WES) with CNV analysis
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
Application of ASCAT Processing to Tumor Samples Using Nexus Copy Number
Analyzing copy number variation in cancer tissues can be a difficult task, but Nexus Copy Number can help!
Investigation of the TCGA LAML dataset using Nexus Copy Number
Learn how to identify relevant common events within the TCGA project and how to leverage the clinical information provided for the samples.
