VSClinical

VSClinical

Golden Helix
+
+

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About

Sano Genetics provides an end-to-end, 360° platform for precision-medicine and clinical-trial research that unifies patient recruitment, genetic testing, consenting, and long-term engagement to dramatically speed up and simplify study workflows. It supports custom protocol development and ethics submission documentation, digital prescreening and consent, and recruitment support through online campaigns, partner networks, and patient-advocacy groups, enabling sponsors and CROs to reach niche patient cohorts or underrepresented populations across multiple geographies. Sano offers at-home, non-invasive saliva-based DNA testing kits (as a cost-effective alternative to clinic blood draws), logistic support for sample collection and processing, reliable genetic and biomarker testing via certified labs, bioinformatics, and return of results, including genetic counselling when needed.

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

Biopharma companies, biotech firms, CROs or research institutions wanting a solution to recruit participants, collect genetic/biomarker data, manage consent and longitudinal engagement

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

Sano
Founded: 2016
United Kingdom
sanogenetics.com

Company Information

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

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StrandOmics

StrandOmics

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Categories

Categories

Integrations

GenomeBrowse
VarSeq

Integrations

GenomeBrowse
VarSeq
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