VSClinical

VSClinical

Golden Helix
+
+

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About

OpenEvidence is an AI-powered clinical decision support platform designed for verified health care professionals, which aggregates, synthesizes, and visualizes peer-reviewed medical evidence to answer point-of-care questions rapidly and reliably. The system covers over 160 specialties and more than 1,000 diseases or therapeutic areas, presenting results grounded in high-quality sources such as JAMA, NEJM, and clinical guidelines. It supports a deep, intuitive search interface that returns evidence-based answers in 5–10 seconds, always with citations, and ensures transparency by surfacing the references behind each answer. In addition to search, OpenEvidence includes features like “Visits,” a module that transcribes patient encounters, enriches documentation with clinical intelligence, drafts notes, and integrates assessment and plan guidance into clinician workflows.

About

VSClinical allows for the clinical interpretation of variants based on ACMG & AMP guidelines. The VSClinical guided workflow enables following the American College of Medical Genetics (ACMG) guidelines used to identify and classify causal variants for inherited disease risk, cancer predisposition, and the diagnosis of rare diseases. The ACMG/AMP joint guidelines for variant interpretation provide a set of criteria to score variants and place them into one of five classification tiers. Following the guidelines requires deep diving into the annotations, genomic context, and existing clinical assertions about every variant. VSClinical provides a tailored workflow to score each relevant criterion while also providing all the bioinformatic, literature and evidence from clinical knowledgebases to assist in the scoring and interpretation process. VSClinical is designed to allow variant scientists to efficiently process variants.

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Audience

Health care professionals and clinicians in search of a tool providing evidence-based clinical decision support, integrated documentation assistance, and access to the latest medical research at the point of care

Audience

Geneticists wanting a tool to identify and classify causal variants for inherited disease risk

Support

Phone Support
24/7 Live Support
Online

Support

Phone Support
24/7 Live Support
Online

API

Offers API

API

Offers API

Screenshots and Videos

Screenshots and Videos

Pricing

Free
Free Version
Free Trial

Pricing

No information available.
Free Version
Free Trial

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Training

Documentation
Webinars
Live Online
In Person

Training

Documentation
Webinars
Live Online
In Person

Company Information

OpenEvidence
Founded: 2022
United States
www.openevidence.com

Company Information

Golden Helix
Founded: 1998
United States
www.goldenhelix.com/products/VarSeq/vsclinical.html

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Categories

Categories

Integrations

GenomeBrowse
VarSeq

Integrations

GenomeBrowse
VarSeq
Claim OpenEvidence and update features and information
Claim OpenEvidence and update features and information
Claim VSClinical and update features and information
Claim VSClinical and update features and information