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Description
OpenEvidence is an advanced clinical decision support platform that leverages artificial intelligence, specifically designed for certified healthcare professionals, to compile, analyze, and present peer-reviewed medical evidence for quick and dependable responses to point-of-care inquiries. This comprehensive system encompasses over 160 specialties and addresses more than 1,000 diseases or therapeutic areas, delivering results supported by reputable sources like JAMA, NEJM, and established clinical guidelines. With a user-friendly and robust search interface, it provides evidence-based answers in just 5 to 10 seconds, complete with citations, while promoting transparency by displaying the references that back each response. Beyond its search capabilities, OpenEvidence boasts functionalities such as "Visits," a module that captures patient interactions, enhances documentation through clinical insights, generates notes, and seamlessly incorporates assessment and planning guidance into the workflows of healthcare providers. Furthermore, this platform ensures that medical professionals are equipped with the most relevant and up-to-date information, thereby improving patient care efficiency and effectiveness.
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
Integrations
GenomeBrowse
VarSeq
Pricing Details
Free
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
OpenEvidence
Founded
2022
Country
United States
Website
www.openevidence.com
Vendor Details
Company Name
Golden Helix
Founded
1998
Country
United States
Website
www.goldenhelix.com/products/VarSeq/vsclinical.html