Average Ratings 0 Ratings
Average Ratings 0 Ratings
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
Yes
API Access
Has API
No
Integrations
GenomeBrowse
No
VarSeq
No
Pricing Details
No price information available.
Free Trial
No
Free Version
No
Pricing Details
No price information available.
Free Trial
Yes
Free Version
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Deployment
Web-Based
Yes
On-Premises
No
iPhone App
No
iPad App
No
Android App
No
Windows
No
Mac
No
Linux
No
Chromebook
No
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Customer Support
Business Hours
Yes
Live Rep (24/7)
No
Online Support
Yes
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
Yes
In Person
Yes
Types of Training
Training Docs
Yes
Webinars
Yes
Live Training (Online)
Yes
In Person
Yes
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
No
In-Database Text Analytics
No
Named Entity Recognition
No
Natural Language Generation (NLG)
No
Open Source Integrations
No
Parsing
No
Part-of-Speech Tagging
No
Sentence Segmentation
No
Stemming/Lemmatization
No
Tokenization
No