VSClinical

VSClinical

Golden Helix
+
+

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About

With more than 70% of healthcare data stored in clinical documents, reports, patient chart, clinician notes and discharge letters, our healthcare specific Natural Language Processing and AI Engine identifies the concepts, attributes and context needed to deliver business insights, optimize billing, identify and stratify patient risks, compute quality metrics or collect patient sentiment and outcome data. Leverage difficult-to-surface or entirely untapped data sources to enhance your clinical research or business intelligence. Leverage our database of thousands of clinical concepts such as genomic biomarkers, symptoms, side effects, and medications. Identify disease characteristics, medications, or risk factors from clinical documents to stratify patients and improve the quality of care. Protect the identity of data subjects while maintaining data utility through document de-identification.

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

Healthcare providers looking for a natural Language Processing platform

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

No information available.
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

Inspirata
Founded: 2014
United States
www.inspirata.com/solutions/healthcare-data-analytics/

Company Information

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

Alternatives

Alternatives

Alissa Interpret

Alissa Interpret

Agilent Technologies
Emedgene

Emedgene

Illumina

Categories

Categories

Population Health Management (PHM) Features

Analytics
Cost-of-Care Analysis
Data Storage
EMR/EHR Integration
Patient Engagement
Patient Identification
Patient Risk Stratification
Patient-Reported Outcomes
Payment Bundling
Predictive Alerts
Test & Treatment Reminders
Utilization Tracking

Integrations

GenomeBrowse
VarSeq

Integrations

GenomeBrowse
VarSeq
Claim Healthcare Data Analytics and update features and information
Claim Healthcare Data Analytics and update features and information
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Claim VSClinical and update features and information