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What is VSClinical?

VSClinical enhances the clinical evaluation of genetic variants by aligning with the guidelines set forth by the ACMG and AMP. Its organized workflow ensures compliance with the standards established by the American College of Medical Genetics (ACMG), which are crucial for identifying and classifying pathogenic variants associated with inherited diseases, cancer risk, and rare diagnoses. The integrated ACMG/AMP guidelines for variant interpretation provide a systematic approach for scoring variants and placing them into one of five classification categories. To effectively implement these guidelines, a comprehensive analysis of annotations, genomic contexts, and existing clinical data for each variant is required. VSClinical simplifies this task by delivering a tailored workflow that assesses each pertinent criterion while offering extensive bioinformatics resources, literary references, and insights from clinical databases to support the scoring and interpretation process. This forward-thinking method aims to improve the productivity of variant scientists as they manage the intricacies of variant analysis and processing. Ultimately, VSClinical emerges as a crucial resource for expediting the understanding and classification of genetic variants within clinical environments, fostering better patient outcomes through informed decision-making. Its role in facilitating efficient variant analysis cannot be overstated, as it significantly contributes to the advancement of personalized medicine.

What is DDxHub?

Diagnosis is the procedure that involves identifying the specific illness or condition responsible for a patient's symptoms and the results of medical tests. DDxHub, known as the Differential Diagnosis Hub, serves as a platform that differentiates a particular disease or condition from others that present with similar symptoms and test outcomes. DDxHub acts as a repository containing extensive descriptions of various diseases. It proves beneficial when aiming to pinpoint the correct diagnosis by allowing users to compare numerous potential conditions. Users have the option to upload their own definitions of diseases to the DDxHub database, enabling them to share this information with other users around the globe in return for disorder descriptions from the community. By joining the ranks of thousands of healthcare professionals and patients who appreciate the advantages of DDxHub’s differential diagnosis and disorder description sharing feature, you can enhance your diagnostic capabilities. Additionally, DDxHub serves as a valuable educational tool for medical students studying clinical therapeutics, providing a comprehensive resource for understanding various disorders.

Media

Media

Integrations Supported

GenomeBrowse
VarSeq

Integrations Supported

GenomeBrowse
VarSeq

API Availability

Has API

API Availability

Has API

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Pricing Information

$39/year/user
Free Trial Offered?
Free Version

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

Golden Helix

Date Founded

1998

Company Location

United States

Company Website

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

Company Facts

Organization Name

Rustemsoft

Company Location

United States

Company Website

smrtx.com

Categories and Features

Categories and Features

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