Ratings and Reviews 0 Ratings

Total
ease
features
design
support

This software has no reviews. Be the first to write a review.

Write a Review

Ratings and Reviews 0 Ratings

Total
ease
features
design
support

This software has no reviews. Be the first to write a review.

Write a Review

Alternatives to Consider

  • Private Internet Access (PIA) Reviews & Ratings
    38 Ratings
    Company Website
  • Shift Reviews & Ratings
    1,375 Ratings
    Company Website
  • MyQ Reviews & Ratings
    197 Ratings
    Company Website
  • QBench Reviews & Ratings
    143 Ratings
    Company Website
  • Kasm Workspaces Reviews & Ratings
    127 Ratings
    Company Website
  • Lockbox LIMS Reviews & Ratings
    72 Ratings
    Company Website
  • WinningBidder.com Reviews & Ratings
    161 Ratings
    Company Website
  • Wave Browser Reviews & Ratings
    52 Ratings
    Company Website
  • Secure Eraser Reviews & Ratings
    14 Ratings
    Company Website
  • Google Cloud BigQuery Reviews & Ratings
    2,016 Ratings
    Company Website

What is GenomeBrowse?

This free software offers exceptional visual displays of your genomic data, enabling you to investigate the specific functions at each base pair within your samples. Operating as a native application on your computer, GenomeBrowse ensures that you do not have to sacrifice speed or quality, providing a uniform experience across various platforms. With performance being a key focus, it delivers a faster and more fluid browsing experience than any other genome browser available. Moreover, GenomeBrowse is fully integrated into the sophisticated Golden Helix VarSeq platform, which is designed for variant annotation and interpretation. If you find the visualization features of GenomeBrowse appealing, you might want to check out VarSeq for additional capabilities such as data filtering, annotation, and analysis before utilizing the same interface for visual representation. The software effectively displays all your alignment data and allows you to view multiple samples at once, which can be incredibly helpful in pinpointing contextually relevant discoveries. This capability makes it an essential resource for researchers aiming to extract more profound insights from their genomic analyses, ultimately enhancing the overall research process. By leveraging these features, users can maximize the impact and utility of their genomic studies.

What is Emedgene?

Emedgene enhances the processes associated with tertiary analysis in the fields of rare disease genomics and various germline research projects. The platform is designed to improve the speed and consistency of interpreting, prioritizing, curating, and producing research reports on user-defined variants. By utilizing explainable AI (XAI) and automation, Emedgene significantly increases efficiency across a range of analysis workflows, including genomes, exomes, virtual panels, and targeted panels. It also aids in merging laboratory operations and next-generation sequencing (NGS) instruments with IT systems, thereby optimizing and securing the entire workflow. As science and technology continue to evolve alongside growing demands, Emedgene provides users with the latest advancements through innovative knowledge graph features, curation tools, and expert assistance throughout their research endeavors. Additionally, laboratories can enhance their throughput without needing to hire extra personnel, thanks to the capabilities of XAI and automated systems. Ultimately, Emedgene supports the implementation of high-throughput workflows for whole genome sequencing (WGS), whole exome sequencing (WES), virtual panels, or targeted panels, all of which seamlessly integrate into the digital infrastructure of any laboratory. This holistic approach ensures that researchers can dedicate their efforts to uncovering new insights while benefiting from reliable technological support that evolves with their needs. By streamlining these complex processes, Emedgene empowers researchers to maximize their potential and drive impactful discoveries in genomics.

Media

Media

Integrations Supported

Illumina DRAGEN Secondary Analysis
VSClinical
VarSeq

Integrations Supported

Illumina DRAGEN Secondary Analysis
VSClinical
VarSeq

API Availability

Has API

API Availability

Has API

Pricing Information

Free
Free Trial Offered?
Free Version

Pricing Information

Pricing not provided.
Free Trial Offered?
Free Version

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Supported Platforms

SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
24 Hour Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

Golden Helix

Date Founded

1998

Company Location

United States

Company Website

www.goldenhelix.com/products/GenomeBrowse/

Company Facts

Organization Name

Illumina

Company Location

United States

Company Website

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

Categories and Features

Categories and Features

Popular Alternatives

XetaBase Reviews & Ratings

XetaBase

Zetta Genomics

Popular Alternatives

VarSeq Reviews & Ratings

VarSeq

Golden Helix
VarSeq Reviews & Ratings

VarSeq

Golden Helix
Alissa Interpret Reviews & Ratings

Alissa Interpret

Agilent Technologies
GenomeStudio Reviews & Ratings

GenomeStudio

Illumina
Alissa Interpret Reviews & Ratings

Alissa Interpret

Agilent Technologies
XetaBase Reviews & Ratings

XetaBase

Zetta Genomics