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ease
features
design
support

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Description

We have been pioneers in the development of clinical NLP platforms and their applications for over 15 years. This has resulted in high precision and accuracy. Our core competency is to interpret unstructured notes accurately and at scale. Tested on billions of real clinical notes and documents. AI that can explain with context, reasoning, and evidence for output. NLP with medical knowledge infused with 4M+ entities and 50M+ relationships. Innovative Machine Learning (ML), & Deep Learning(DL) models were used to build this NLP. Use a foundation of rich ontologies and clinician-specific terminologies. We can understand, interpret, and extract context & significance from the inconsistent, inconsistent, and non-standard data contained in medical documents. Our clinical domain experts continually infuse knowledge graphs to our NLP by mapping all clinical entities and their relationship between them. We have more than 4,000,000 entities and 50,000,000 relationships.

Description

VSClinical facilitates the clinical analysis of genetic variants in accordance with ACMG and AMP guidelines. Its structured workflow supports adherence to the American College of Medical Genetics (ACMG) standards, which are essential for identifying and categorizing pathogenic variants related to inherited disease risk, cancer susceptibility, and rare disease diagnosis. The combined ACMG/AMP guidelines for variant interpretation establish a framework for scoring variants and categorizing them into one of five classification levels. Implementing these guidelines necessitates a thorough examination of annotations, genomic contexts, and pre-existing clinical insights for each variant. VSClinical streamlines this process by offering a customized workflow that evaluates each relevant criterion and supplies comprehensive bioinformatics, literature references, and clinical knowledgebase evidence to aid in the scoring and interpretation of variants. This innovative approach is designed to enhance the efficiency of variant scientists as they navigate the complexities of variant processing and analysis. Overall, VSClinical stands out as a vital tool for accelerating the understanding and classification of genetic variants in clinical settings.

API Access

Has API

API Access

Has API

Screenshots View All

Screenshots View All

Integrations

GenomeBrowse
VarSeq

Integrations

GenomeBrowse
VarSeq

Pricing Details

No price information available.
Free Trial
Free Version

Pricing Details

No price information available.
Free Trial
Free Version

Deployment

Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook

Deployment

Web-Based
On-Premises
iPhone App
iPad App
Android App
Windows
Mac
Linux
Chromebook

Customer Support

Business Hours
Live Rep (24/7)
Online Support

Customer Support

Business Hours
Live Rep (24/7)
Online Support

Types of Training

Training Docs
Webinars
Live Training (Online)
In Person

Types of Training

Training Docs
Webinars
Live Training (Online)
In Person

Vendor Details

Company Name

RAAPID INC

Founded

2022

Country

United States

Website

www.raapidinc.com

Vendor Details

Company Name

Golden Helix

Founded

1998

Country

United States

Website

www.goldenhelix.com/products/VarSeq/vsclinical.html

Product Features

Natural Language Processing

Co-Reference Resolution
In-Database Text Analytics
Named Entity Recognition
Natural Language Generation (NLG)
Open Source Integrations
Parsing
Part-of-Speech Tagging
Sentence Segmentation
Stemming/Lemmatization
Tokenization

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