+
+

Related Products

  • Google Cloud Speech-to-Text
    366 Ratings
    Visit Website
  • Vibe Retail
    89 Ratings
    Visit Website
  • Admin By Request Endpoint Privilege Management
    100 Ratings
    Visit Website
  • InEight
    136 Ratings
    Visit Website
  • Onetrace
    4 Ratings
    Visit Website
  • QBench
    152 Ratings
    Visit Website
  • R3 Contract Management for GovCon
    1 Rating
    Visit Website
  • Planview Software Product Delivery
    2 Ratings
    Visit Website
  • Square Payments
    10,139 Ratings
    Visit Website
  • Hyperproof
    350 Ratings
    Visit Website

About

Folklore is Helena Bioinformatics’ clinical variant interpretation platform for genomics laboratories. It combines VCF analysis, curated evidence, literature, phenotype, inheritance and prioritisation in a traceable specialist workflow. Panels, exomes and genomes include nuclear, mitochondrial and structural/copy-number variants with ACMG/AMP, MMDWG and Riggs frameworks. Its separate public, read-only Folklore MCP 1.5.0 offers seven tools for supported GRCh38 germline variant evidence, literature, ClinGen gene-disease associations and optional support. New get_gene_disease_associations and search_disease_genes tools accept gene/HGNC or disease/MONDO queries and preserve inheritance, source classifications and provenance. MCP uses Streamable HTTP without an account or API key; it accepts no patient data, VCF uploads or batch analysis. Results support qualified professional review and are not diagnoses or treatment recommendations.

About

Upload your clients’ health data to instantly generate risk scores, analysis summaries & personalized supplements, diet and lifestyle recommendations. Get better results by offering clients scientifically accurate and personalized recommendations based on their DNA, labs and environmental data. See more clients and improve retention with an easy-to-use platform that allows you to streamline your health services. See which genes are playing a role in your clients’ health issues. Build a plan to address the problem genes using the AI-generated list of prioritized recommendations. SelfDecode Labs is a simple tool giving more insight into your clients’ lab results. Order lab tests or upload results to see where levels fall related to the functional range, get suggestions to improve them & track them over time. Add recommendations to your clients’ easy-to-follow regimen. Track progress and make changes based on what’s working.

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Audience

Clinical genomics teams, molecular diagnostics laboratories, variant scientists, bioinformaticians, researchers and academic or healthcare organizations evaluating public genomic evidence.

Audience

Healthcare industry in need of an AI platform that provides personalized health recommendations

Support

Phone Support
24/7 Live Support
Online

Support

Phone Support
24/7 Live Support
Online

API

Offers API

API

Offers API

Screenshots and Videos

Screenshots and Videos

Pricing

No information available.
Free Version
Free Trial

Pricing

$199 per month
Free Version
Free Trial

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Training

Documentation
Webinars
Live Online
In Person

Training

Documentation
Webinars
Live Online
In Person

Company Information

Helena Bioinformatics
Bulgaria
folklore.helena.bio

Company Information

SelfDecode
Founded: 2016
United States
selfdecode.com/en/selfdecode-pro/

Alternatives

VSClinical

VSClinical

Golden Helix

Alternatives

VarSeq

VarSeq

Golden Helix
QIAGEN CLC Genomics Workbench

QIAGEN CLC Genomics Workbench

QIAGEN Digital Insights

Categories

Categories

Integrations

No info available.

Integrations

No info available.
Claim Folklore Clinical Variant Interpretation and update features and information
Claim Folklore Clinical Variant Interpretation and update features and information
Claim SelfDecode and update features and information
Claim SelfDecode and update features and information