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About

2bPrecise delivers transformative point-of-care solutions that serve as the foundation for scalable precision medicine success. Patient not responding to first-line treatments for common conditions? Pharmacogenomics helps you identify medications that are safer and more effective. Fingertip access to test results helps eliminate “trial-and-error” prescribing practices, and accelerates patient response. Detailed genetics-focused data-gathering tools help you capture and expose risk. In-workflow Pedigree visualization allows you to identify candidates that could benefit from genetic testing, and lead you to the best course of treatment. Patient presents you with a diagnostic dilemma (e.g., symptoms such as seizures or syncope correlated with multiple conditions)? Germline tests hone in on heritable factors that can inform diagnoses. Access to meaningful and actionable results during clinical decision-making enables you to initiate preventive measures.

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.

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

Hospitals and healthcare providers in need of a platform to simplify, condense and extract patient information

Audience

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

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

No information available.
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

2bPrecise
Founded: 2016
United States
2bprecisehealth.com

Company Information

Helena Bioinformatics
Bulgaria
folklore.helena.bio

Alternatives

Progeny Clinical

Progeny Clinical

Progeny Software

Alternatives

VSClinical

VSClinical

Golden Helix
VarSeq

VarSeq

Golden Helix
QuicDoc

QuicDoc

DocuTrac
QIAGEN CLC Genomics Workbench

QIAGEN CLC Genomics Workbench

QIAGEN Digital Insights
Emedgene

Emedgene

Illumina

Categories

Categories

Integrations

No info available.

Integrations

No info available.
Claim 2bPrecise and update features and information
Claim 2bPrecise and update features and information
Claim Folklore Clinical Variant Interpretation and update features and information
Claim Folklore Clinical Variant Interpretation and update features and information