BioDiscovery Webinars

Product: Nxclinical

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.

A retrospective evaluation of 211 clinical referrals for intellectual disability testing

This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.

Integrated analysis of SNVs, CNVs, and AOH facilitates accurate diagnosis in Mendelian disorders & pediatric cancers

This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.