BioDiscovery Webinars

Topic: Clinical

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 recording

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 Recording

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

Increased diagnostic accuracy for Mendelian disorders and pediatric cancers through integrated review of SNVs, CNVs and regions of homozygosity Recording

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

Combined Analysis and Interpretation of CNV, AOH, and Seq Var of FFPE Cancer Samples from a Solid Tumor NGS Panel Recording

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