Reveal all classes of structural variants using Bionano’s optical genome mapping Stratys™ System. Explore the Stratysphere!

Unlocking the Mysteries of Rare Diseases with Optical Genome Mapping: Insights from ESHG 2024

Events | 2024-07-09
Genetic disease
Saphyr System
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All Blogs

Copy Number and Loss of Heterozygosity Analysis in Tumors

Education | 2019-02-02
Oncology
Solid tumors
NxClinical Software
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OMIM data in NxClinical

Education | 2018-09-20
Genetic disease
Technology development
NxClinical Software
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Significant Cost Savings with Single NGS Test vs. Other Strategies

2018-07-19
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Trio analysis in NxClinical – Heritable retinal dystrophies in the Costa Rican population Case Study

2018-05-02
NxClinical Software
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Clinical Conversation – Ingrid Simonic: Optimizing and Consolidating Multiple Testing Strategies to Increase Efficiency with Increasing Testing Demand

2018-04-30
NxClinical Software
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NxClinical February track updates

2018-02-16
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How are systematic correction files used for correcting probe values?

2017-12-06
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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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