Best research platform for variant curation jobs

Finally, there’s a way for variant curators to search published genomic literature without missing evidence and wasting time.

A person on a laptop using Mastermind to conduct research for genes and variants.

Are you confident you have access to all the genomic literature you need for your variant scientist job?

A 2020 study* reported that laboratories disagreed on a variant’s classification 46% of the time, with 23% of those discrepancies being clinically impactful. Access to comprehensive genetic evidence is critical for proper diagnosis and variant curation jobs.

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Mastermind Genomic Intelligence Platform

The Most Comprehensive Source of Published Genomic Literature

Designed for Variant Curators and Genomicists

Reduce Turnaround Time

Quickly identify and review the genetic evidence, clinically prioritized with insight into each genomic article to speed variant interpretation for curators.

Increase Diagnostic Yield

Access 100X more genomic evidence and 20X more variants than other sources to find relevant genomic articles, resolve more VUSs, and diagnose more patients.

Accelerate Throughput

Optimize your variant curation job by rapidly prioritizing variants of disease-causing genes, simplifying your analysis and enabling a more targeted approach.

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Why is searching for genomic literature so hard?

Legacy Nomenclature Makes Genomic Evidence Hard to Find

More than 74% of the genomic variants in publications are still in non-normalized forms1, making citations hard to find, even in resources like NCBI’s PubMed.

Data is Hidden in the Body and Supplemental Text of Genomic Articles

Fewer than 6% of variants are identified in the title or abstract in NCBI’s PubMed, the remainder present in the full-text or supplemental files1.

1. https://pubmed.ncbi.nlm.nih.gov/33281875/