Helix Labs
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About
Helix Labs offers advanced pathogenicity predictions for protein variants, emphasizing accuracy and comprehensive insights. Utilizing high-quality 3DM data, the tool collaborates AI technology with human expertise to deliver predictions that distinguish pathogenic from benign variants. Helix's capabilities are structured for research purposes, allowing scientists to access detailed variant reports and integrate seamlessly into their workflows. With extensive training on clinically relevant genes and transparent decision-making processes, Helix is designed for use by clinical, pharmacological, and academic professionals. It also offers an API for streamlined data access and has plans for continuous improvement.
Platform
Features
• state-of-the-art pathogenicity predictions
• transparent decision-making process
• high-quality 3dm data integration
• in-depth variant reports
• accessible via api
FAQs
Who can use Helix?
Helix is used by professionals in clinical, pharmacological, and health sectors for research purposes.
What is Helix used for?
It analyzes human missense variants for clinical diagnostics and provides in-depth variant reports.
How do I access Helix data?
Data can be accessed via the website, API, or flat file under specific conditions.
Can I test Helix?
Yes, by contacting Helix to assess results on your dataset in a secure environment.
What types of variants does Helix predict?
Currently, only missense variants are predicted, with plans to integrate indel predictions.
What is the recommended cutoff for Helix scores?
The optimized cutoff is 0.5, with below indicating benign and above indicating pathogenic predictions.
How does Helix compare to other predictors?
Helix is superior, providing in-depth reports and is consistently updated compared to competitors.
Are Helix predictions available for other organisms?
Yes, contact Helix for discussion on options.
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