VSClinical

VSClinical

Golden Helix
+
+

Related Products

  • Proton Pass
    31,993 Ratings
    Visit Website
  • Semrush
    5,701 Ratings
    Visit Website
  • Qloo
    23 Ratings
    Visit Website
  • CallTrackingMetrics
    845 Ratings
    Visit Website
  • Quaeris
    6 Ratings
    Visit Website
  • CodeSignal
    1,631 Ratings
    Visit Website
  • Skillfully
    2 Ratings
    Visit Website
  • Encompassing Visions
    13 Ratings
    Visit Website
  • Sogolytics
    863 Ratings
    Visit Website
  • Google Cloud BigQuery
    1,861 Ratings
    Visit Website

About

Generate greater return on research and improve team productivity. Extend private and public data across teams with interactive data visualization. Rosalind is the only multi-tenant SaaS platform designed for scientists. Analyze, interpret, share, plan, validate, and generate new hypotheses. Code-free visualization, AI-powered interpretation, best-in-class collaboration. Scientists of every skill level can benefit from ROSALIND since no programming or bioinformatics skills are required. With powerful downstream analysis and collaboration, ROSALIND is a discovery platform and data hub connecting experiment design, quality control, and pathway exploration. ROSALIND automatically manages tens of thousands of compute cores and petabytes of storage to dynamically scale up and down for every experiment to deliver results. Instantly share results with other scientists across the globe with audit tracking so everyone can focus on the interpretation, not the processing.

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

Academic researchers wanting a solution to analyze, interpret, share, and validate data

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

$3,250 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

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

ROSALIND
Founded: 2013
United States
www.rosalind.bio/

Company Information

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

Alternatives

Partek Flow

Partek Flow

Partek

Alternatives

Alissa Interpret

Alissa Interpret

Agilent Technologies
Emedgene

Emedgene

Illumina
OmicsBox

OmicsBox

BioBam Bioinformatics S.L.

Categories

Categories

Integrations

GenomeBrowse
VarSeq

Integrations

GenomeBrowse
VarSeq
Claim ROSALIND and update features and information
Claim ROSALIND and update features and information
Claim VSClinical and update features and information
Claim VSClinical and update features and information