Don’t Miss Variants: Upgrading From the Cited Variants Reference to the Mastermind API

In this blog, chief technology officer Steve Schwartz describes the limitations of the Mastermind Cited Variants Reference (CVR) that affect genomic analyses, and how the integration of Mastermind’s API can help surmount them.

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Rapid Variant Interpretation with the Mastermind Relevancy Score

The key to rapid and accurate literature curation for clinical interpretation and therapeutic discovery is standardizing and optimizing the review process. The Mastermind Genomic Search Engine meets this need with a collection of sophisticated algorithms that prioritize search results by relevance. This proprietary process is called the Mastermind Relevancy Score.

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Mastermind Updates: Search Companion

We have just released a major update to Search Companion, our Chrome extension for Mastermind. Key elements of this enhancement include functionality on eight new platforms, a more intuitive interface with deeper data, plus access is now available to all Chrome users, including those without a Mastermind account.

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Mastermind Update: Improved Article Icon Attributes

We often blog about the significant strides we’ve made to organize and make sense of genomic knowledge contained within the primary evidence of the medical literature. And there is certainly a lot to talk about. But we thought it’d be interesting to give insight into how much attention and effort goes into even the smallest …

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Mastermind Connection: Nostos Genomics AION Platform

Nostos Genomics’ AION is now integrated with the Mastermind Genomic Search Engine. This blog will show how AION users can quickly view Mastermind publication search results within the platform in just a few steps.

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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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