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Copy Number and AOH Detection from Next-Generation Sequencing

| 2023-05-09
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A first-of-its-kind clinical research genetics knowledgebase – Accelerate your case review with NxClinical

Impact | 2021-12-16
Genetic disease
Oncology
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Hello, ACMG scoreboard. Goodbye, external calculator tools

Impact | 2021-10-06
Cytogenomics
Genetic disease
Molecular genomics
Technology development
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The DGV score and so much more

Impact | 2021-09-02
Cytogenomics
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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
Genetic disease
Molecular genomics
Technology development
NxClinical Software
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Labs Meeting a Minimum Standard of Data Sharing Identified by ClinGen

2017-07-20
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How does clustering work in Nexus Copy Number?

2017-06-29
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Comparison of the BAM (multiscale reference) algorithm to other methods for CNV detection from NGS

2017-03-29
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Mosaic copy number aberrations in healthy individuals

2017-01-05
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NxClinical Software Increases Efficiency in the Reporting Process at CombiMatrix | Invitae

2016-10-05
NxClinical Software
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What are systematic correction files?

2016-09-02
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Sample Attributes: How adding annotation can streamline your workflow

2016-08-26
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For CNV analysis, how do I combine data from different sources into a single Nexus Copy Number project?

2016-08-05
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Why can’t I find this gene? Why don’t these genomic coordinates match?

2016-06-15
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Can I Get Quality Copy Number Results from NGS data?

2016-04-28
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Paired Analysis

2016-02-25
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