Folklore Clinical Variant InterpretationHelena Bioinformatics
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About
Folklore is Helena Bioinformatics' research-use-only platform for clinical variant interpretation. It helps genomic professionals examine public variant evidence, literature, clinical assertions, population information and guideline-relevant evidence in a structured workflow. Folklore also provides a public read-only MCP adapter for agent-based evidence discovery. It does not diagnose, recommend treatment or replace expert review. The platform is intended for clinical genomics teams, molecular diagnostics laboratories, researchers, bioinformaticians and variant scientists.
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About
SeqOne is an AI-powered genomic analysis platform designed to help molecular laboratories, clinical teams, biologists, and geneticists transform complex next-generation sequencing data into fast, precise, and actionable clinical insights to support personalized medicine diagnostics. It streamlines end-to-end genomic workflows, from raw sequencing files to variant interpretation and reporting, by automating routine pipeline tasks, integrating seamlessly with lab systems, and using advanced AI models such as DiagAI to rank and highlight disease-relevant variants with explainable scores, reducing manual effort and turnaround time. SeqOne supports germline and somatic analyses across applications, including oncology, rare and inherited diseases, and infectious disease detection, combining premium annotation databases and standardized interpretation guidelines to ensure clinical-grade accuracy within an intuitive user interface that scales via secure cloud.
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Platforms Supported
Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook
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Platforms Supported
Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook
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Audience
Clinical genomics teams, molecular diagnostics laboratories, variant scientists, bioinformaticians, researchers and academic or healthcare organizations evaluating public genomic evidence.
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Audience
Molecular diagnostic labs and clinical genomics teams needing AI-driven tools to automate NGS data analysis and deliver rapid, accurate genomic insights for healthcare decision-making
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Support
Phone Support
24/7 Live Support
Online
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Support
Phone Support
24/7 Live Support
Online
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API
Offers API
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API
Offers API
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Screenshots and VideosNo images available
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Pricing
No information available.
Free Version
Free Trial
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Pricing
No information available.
Free Version
Free Trial
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Reviews/
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Reviews/
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Training
Documentation
Webinars
Live Online
In Person
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Training
Documentation
Webinars
Live Online
In Person
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Company InformationHelena Bioinformatics
Bulgaria
folklore.helena.bio
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Company InformationSeqOne
Founded: 2017
France
www.seqone.com
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Integrations
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Integrations
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