The Importance of Automated Semantic Search for Copy Number Variants (CNVs)

Continuing our discussion on CNV search in Mastermind, we’ll discuss the practical advantages of automated semantic searches, and explore how Mastermind’s powerful algorithm resolves sensitivity and specificity issues associated with multiple CNV nomenclatures.

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Navigating CNVs in Mastermind with the New “Stacked Pancake” Plot

Mastermind quickly sorts and prioritizes CNV results with automated, semantic search – but how can this be visualized? This blog will introduce our new “Stacked Pancake” Plot for CNVs, and will explore how it adds even more flexibility to your experience.

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Mastermind Update: Genomic Associations Interface

This major update to the Mastermind Genomic Search Engine provides a new interface to find, connect, explore, and understand the links between genomic concepts of interest.

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Mastermind Connection: DNASTAR Lasergene Software

DNASTAR’s Variant Annotation Database (VAD), included in Lasergene Genomics, is now integrated with the Mastermind Genomic Search Engine. With this integration, Lasergene users can now quickly and easily search and cross-reference NGS variant data from millions of PubMed publications.

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Mastermind Update: More Intuitive Search

The latest update to the Mastermind Genomic Search Engine includes enhancements to the search functionality, which provides a more effective and intuitive search experience.

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Mastermind Update: Mastermind CNV Search

The Mastermind Genomic Search Engine now includes searching by Copy Number Variation (CNV). This new feature accelerates the diagnosis and interpretation of results for patients with genetic disease. Here’s how to find CNVs in Mastermind.

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