VSClinicalGolden Helix
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Related Products
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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.
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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.
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Platforms Supported
Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook
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Platforms Supported
Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook
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Audience
Biopharma companies, biotech firms, CROs or research institutions wanting a solution to recruit participants, collect genetic/biomarker data, manage consent and longitudinal engagement
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Audience
Geneticists wanting a tool to identify and classify causal variants for inherited disease risk
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Support
Phone Support
24/7 Live Support
Online
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Support
Phone Support
24/7 Live Support
Online
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API
Offers API
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API
Offers API
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Screenshots and Videos |
Screenshots and Videos |
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Pricing
No information available.
Free Version
Free Trial
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Pricing
No information available.
Free Version
Free Trial
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Reviews/
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Reviews/
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Training
Documentation
Webinars
Live Online
In Person
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Training
Documentation
Webinars
Live Online
In Person
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Company InformationSano
Founded: 2016
United Kingdom
sanogenetics.com
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Company InformationGolden Helix
Founded: 1998
United States
www.goldenhelix.com/products/VarSeq/vsclinical.html
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Categories |
Categories |
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Integrations
GenomeBrowse
VarSeq
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