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What is OmicsBox?

OmicsBox stands out as a premier bioinformatics platform that delivers comprehensive data analysis capabilities for genomes, transcriptomes, and metagenomes, in addition to facilitating genetic variation research. This software, widely adopted by prominent research institutions globally, enables scientists to handle extensive and complex datasets while optimizing their analytical workflows. Its design emphasizes efficiency and user-friendliness, providing robust tools that help extract meaningful biological insights from omics data. The application is segmented into various modules, each tailored with distinct tools and functionalities aimed at conducting specific analyses, including de novo genome assembly, genetic variation assessments, differential expression evaluations, and taxonomic classifications of microbiomes, along with insightful result interpretations and engaging visualizations. Notably, the functional analysis module incorporates the well-regarded Blast2GO annotation method, making OmicsBox an excellent resource for research involving non-model organisms, thereby broadening its applicability in the scientific community. This versatility positions OmicsBox as an essential tool for researchers looking to advance their understanding of complex biological systems.

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.

Media

Media

Integrations Supported

VSClinical
VarSeq

Integrations Supported

VSClinical
VarSeq

API Availability

Has API

API Availability

Has API

Pricing Information

€100/month/seat
Free Trial Offered?
Free Version

Pricing Information

Free
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

BioBam Bioinformatics S.L.

Date Founded

2011

Company Location

Spain

Company Website

www.biobam.com

Company Facts

Organization Name

Golden Helix

Date Founded

1998

Company Location

United States

Company Website

www.goldenhelix.com/products/GenomeBrowse/

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