April 30, 2018

Webinars
Combined Analysis and Interpretation of CNV, AOH, and Seq Var of FFPE Cancer Samples from a Solid Tumor NGS Panel Recording
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September 23, 2016

Webinars
Gene Prioritization in Regions of Homozygosity
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December 10, 2020

Webinars
Increasing the yield of exome sequencing with copy number variant analysis
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December 19, 2019

Webinars
A retrospective evaluation of 211 clinical referrals for intellectual disability testing recording
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December 10, 2019

Webinars
Integrated analysis of SNVs, CNVs, and AOH facilitates accurate diagnosis in Mendelian disorders & pediatric cancers Recording
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May 31, 2019

Webinars
Increased diagnostic accuracy for Mendelian disorders and pediatric cancers through integrated review of SNVs, CNVs and regions of homozygosity Recording
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May 14, 2018

Webinars
Highlights of NxClinical 4.1: Improved Sequence Variant Interpretation and Support for the Newest Array Platforms Recording
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June 30, 2017

Webinars
Downstream Research Analysis of Copy Number from NGS in Cancer Samples
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May 1, 2017

Webinars
Challenges and Solutions to Copy Number Estimation from Whole Exome Sequencing in Tumors
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March 20, 2017

Webinars
A New Understanding of the Genetic Basis of Pregnancy Loss: What Large-scale Cytogenomic Analysis is Revealing
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