VSClinical

VSClinical

Golden Helix
+
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About

Take a peek at what is really going on in your company without the stress of a complex project. It doesn’t matter how many systems and data sources your processes traverse, with data virtualization and our partnership with Denodo, we can follow them from start to finish. With our flexible APIs and our connectors, you can be up and running in no time. User-friendly interface, pre-built filters, and an easy-to-learn query language let you focus on what’s important: the processes, not the tool. Discover how your processes behave. Start with the most frequent execution and expand your view to incorporate all variants. Choose how many variants you want to aggregate and display frequencies and duration metrics. You will have unprecedented insights into the actual performance of your process model. Identify outliers and extreme variants in the blink of an eye thanks to the contextual information panel and you will soon be discovering the secret life of the firm.

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

Companies seeking a solution to improve their operational performance processes

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

€500 per month
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

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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

Inverbis
Founded: 2020
Spain
web.inverbisanalytics.com

Company Information

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

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Categories

Categories

Integrations

Denodo
GenomeBrowse
VarSeq

Integrations

Denodo
GenomeBrowse
VarSeq
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