RAAPID

RAAPID

RAAPID INC
VSClinical

VSClinical

Golden Helix
+
+

Related Products

  • RXNT
    552 Ratings
    Visit Website
  • Elation Health
    88 Ratings
    Visit Website
  • Aesthetic Insight
    10 Ratings
    Visit Website
  • Qloo
    23 Ratings
    Visit Website
  • AdvancedMD
    2 Ratings
    Visit Website
  • kama.ai
    9 Ratings
    Visit Website
  • Filejet
    51 Ratings
    Visit Website
  • LM-Kit.NET
    29 Ratings
    Visit Website
  • Gravity Software
    45 Ratings
    Visit Website
  • Google AI Studio
    30 Ratings
    Visit Website

About

Over 15+ years, we have been the pioneers in building successful clinical NLP platforms & their applications that delivers high accuracy and precision rates. Our core capability is to interpret unstructured notes, accurately and at scale. Tried & tested on billions of diverse and real clinical notes & documents. Explainable AI with reasoning, context & evidence for output. Medical knowledge infused NLP with 4M+ entities & 50M+ relationships. Built using innovative Machine Learning (ML) & Deep Learning (DL) models. Leverage a foundation of rich ontologies & clinician-specific terminologies. We have the ability to understand, interpret and extract context & meaning from the messy, inconsistent, non-standardized data within medical documents. Our Clinical domain experts continuously infuse knowledge graphs into our NLP by mapping all the clinical entities and the relationship between them. So far, we have more than 4 million entities and 50 million relationships.

About

VSClinical allows for the clinical interpretation of variants based on ACMG & AMP guidelines. The VSClinical guided workflow enables following the American College of Medical Genetics (ACMG) guidelines used to identify and classify causal variants for inherited disease risk, cancer predisposition, and the diagnosis of rare diseases. The ACMG/AMP joint guidelines for variant interpretation provide a set of criteria to score variants and place them into one of five classification tiers. Following the guidelines requires deep diving into the annotations, genomic context, and existing clinical assertions about every variant. VSClinical provides a tailored workflow to score each relevant criterion while also providing all the bioinformatic, literature and evidence from clinical knowledgebases to assist in the scoring and interpretation process. VSClinical is designed to allow variant scientists to efficiently process variants.

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

Healthcare providers in need of a tool to manage terminologies, extract context and meaning from documents, and get insights

Audience

Geneticists wanting a tool to identify and classify causal variants for inherited disease risk

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

RAAPID INC
Founded: 2022
United States
www.raapidinc.com

Company Information

Golden Helix
Founded: 1998
United States
www.goldenhelix.com/products/VarSeq/vsclinical.html

Alternatives

Alternatives

Alissa Interpret

Alissa Interpret

Agilent Technologies
Micromedex

Micromedex

Merative
StrandOmics

StrandOmics

Strand Life Sciences

Categories

Categories

Integrations

GenomeBrowse
VarSeq

Integrations

GenomeBrowse
VarSeq
Claim RAAPID and update features and information
Claim RAAPID and update features and information
Claim VSClinical and update features and information
Claim VSClinical and update features and information