BioDiscovery Webinars

Topic: Ngs

Highlights of NxClinical 4.1: Improved Sequence Variant Interpretation and Support for the Newest Array Platforms Recording

Dr. Soheil Shams discusses the highlights of NxClinical 4.1: Improved Sequence Variant Interpretation and Support for the Newest Array Platforms Recording

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.

NxClinical 4.0 – CNV, SeqVar, and AOH from a single NGS assay

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

Downstream Research Analysis of Copy Number from NGS in Cancer Samples

This webinar is geared towards those working on research projects and want to know what types of advanced analyses can be performed in Nexus Copy Number.

Challenges and Solutions to Copy Number Estimation from Whole Exome Sequencing in Tumors

This webinar is geared towards those requiring copy number results from low coverage sequencing results (shallow/targeted) and/or from normal coverage WGS/WES results.

A new method to estimate copy number from NGS for both shallow/targeted sequencing and normal coverage WGS/WES data 

This webinar is geared towards those requiring copy number results from low coverage sequencing results (shallow/targeted) and/or from normal coverage WGS/WES results.

Gene Prioritization in Regions of Homozygosity

This webinar is geared towards those performing genomic variation analysis and interpretation in a cytogenomics lab.

Detecting CNVs from Whole Exome Sequencing Data Using Nexus Copy Number

Learn a new way of inferring CNVs from whole exome sequencing data using nexus copy number software, and also see how this method compares to other methods.

Whole Genome MAQ in Nexus Copy Number software – A fast, simple, and integrated tool for CNV validation

Bert Eussen gives some helpful hints for those studying copy number variation from arrays or NGS and need an alternate method for validation of CNVs.

Constitutional and Cancer Sample Review for Cytogeneticists: Copy Number and Sequence Variant Analysis Using Nexus Copy Number

Learn how CNV, LOH and sequence variant analysis tools for cytogeneticists allow for better decisions on the significance of events being detected.Learn how CNV, LOH and sequence variant analysis tools for cytogeneticists allow for better decisions on the significance of events being detected.

Copy Number Estimation from Exome and Genome Sequencing Data

This webinar discusses some relatively simple approaches for copy number estimation from sequencing data, give some examples, and show how to load these data into Nexus Copy Number software.

Integrated analysis of sequence variations and copy number in TCGA data with the new Nexus Copy Number

Get an integrated analysis of copy number and sequence variation using data from The Cancer Genome Atlas (TCGA), and learn how CNV, allelic events, and seq. variations can aid in the discovery process in cancer studies.