Average Ratings 0 Ratings
Average Ratings 0 Ratings
Description
The PAI-SP serves as a robust diagnostic and interpretive tool, equipped with a range of modules tailored to fulfill diverse assessment requirements. It establishes a unified framework of essential functions and features that are consistent across all activated PAI modules. This includes tools for navigation, file management, report modification, and remote updates via telephone or the Internet for the administrative counters displayed on screen. The PAI forms generate thorough, valuable, and precise reports, ranging from 10 to 15 pages for PAI Clinical Interpretive Reports, or shorter 2 to 4-page PAS Score Reports. Users of the PAI Plus reports benefit from an enhanced interpretation method that incorporates a DSM-5 update, an optional Alternative Model for Personality Disorders Profile, and 15 additional supplemental indices. Moreover, users can enrich their client profiles with context-specific normative profile overlays and can compare client scores to targeted norm groups using z scores, thereby offering a deeper insight into the assessment results. This comprehensive approach significantly enhances the interpretive capabilities of the PAI-SP.
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
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
PAR
Website
www.parinc.com
Vendor Details
Company Name
Golden Helix
Founded
1998
Country
United States
Website
www.goldenhelix.com/products/VarSeq/vsclinical.html
Product Features
Mental Health
Appointment Reminders
Appointment Scheduling
Assessment & Treatment Plans
Billing & Invoicing
Claims Management
E-Prescribing
EDI
EMR / EHR
HIPAA Compliant
Inpatient / Residential
Multi-Provider Practice
Patient Portal
Personnel Management
Progress Notes
Single Provider Practice