Emedgene

Emedgene

Illumina
VSClinical

VSClinical

Golden Helix
+
+

Related Products

  • gPanel
    61 Ratings
    Visit Website
  • LabWare LIMS
    113 Ratings
    Visit Website
  • SciSure
    295 Ratings
    Visit Website
  • ScalaHosting
    2,287 Ratings
    Visit Website
  • FinOpsly
    3 Ratings
    Visit Website
  • Hostinger
    58,737 Ratings
    Visit Website
  • Graylog
    383 Ratings
    Visit Website
  • MetaLocator
    24 Ratings
    Visit Website
  • Certainty Software
    66 Ratings
    Visit Website
  • Ango Hub
    15 Ratings
    Visit Website

About

Emedgene streamlines your tertiary analysis workflows for rare disease genomics and other germline research applications. Emedgene is designed to accelerate the time and certainty in user-defined variant interpretation, prioritization, curation, and research report generation. Enable greater efficiency from your tertiary analysis workflows with explainable AI (XAI) and automation supporting genomes, exomes, virtual panels, and targeted panels. Unify your laboratory and NGS instrumentation with your IT systems to simplify and secure your complete workflow. Confidently keep pace with evolving science, technology, and demand with up-to-date knowledge graph options, curation capabilities, and a team of experts to support your journey. Increase throughput without increasing headcount using explainable AI (XAI) and automated workflows. Implement a high throughput WGS, WES, virtual panel, or targeted panel workflow that is integrated into your lab's digital ecosystem.

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 professionals in search of a tool to unlock genomic insights for hereditary disease

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

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

Illumina
United States
www.illumina.com/products/by-type/informatics-products/emedgene.html

Company Information

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

Alternatives

VarSeq

VarSeq

Golden Helix

Alternatives

Alissa Interpret

Alissa Interpret

Agilent Technologies
Alissa Interpret

Alissa Interpret

Agilent Technologies
StrandOmics

StrandOmics

Strand Life Sciences
XetaBase

XetaBase

Zetta Genomics
Emedgene

Emedgene

Illumina

Categories

Categories

Integrations

GenomeBrowse
Illumina DRAGEN Secondary Analysis
VarSeq

Integrations

GenomeBrowse
Illumina DRAGEN Secondary Analysis
VarSeq
Claim Emedgene and update features and information
Claim Emedgene and update features and information
Claim VSClinical and update features and information
Claim VSClinical and update features and information