Watch the exceptional presentations, plus the Q&A panel discussions, on demand from Symposium 2023!

Copy Number and AOH Detection from Next-Generation Sequencing

| 2023-05-09

A first-of-its-kind clinical research genetics knowledgebase – Accelerate your case review with NxClinical

Impact | 2021-12-16
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Combined CNV and SNV detection from NGS panels in a clinical setting – a single test system is within reach!

Education | 2017-09-21

Labs Meeting a Minimum Standard of Data Sharing Identified by ClinGen

2017-07-20

How does clustering work in Nexus Copy Number?

2017-06-29

Comparison of the BAM (multiscale reference) algorithm to other methods for CNV detection from NGS

2017-03-29

Mosaic copy number aberrations in healthy individuals

2017-01-05

NxClinical Software Increases Efficiency in the Reporting Process at CombiMatrix | Invitae

2016-10-05

What are systematic correction files?

2016-09-02

Sample Attributes: How adding annotation can streamline your workflow

2016-08-26

For CNV analysis, how do I combine data from different sources into a single Nexus Copy Number project?

2016-08-05

Why can’t I find this gene? Why don’t these genomic coordinates match?

2016-06-15

Can I Get Quality Copy Number Results from NGS data?

2016-04-28

Paired Analysis

2016-02-25

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