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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 Alissa Interpret?

Alissa Interpret is an all-encompassing genomic data interpretation tool aimed at improving clinical decision-making processes. By leveraging its adaptable CGH and NGS tertiary analysis platform, users can enhance productivity, shorten turnaround times, and maintain compliance with regulatory requirements. This software achieves peak operational effectiveness when paired with Agilent’s specialized SureSelect NGS reagents, the intuitive Alissa Reporter for secondary NGS analysis, Magnis automated workflows, and TapeStation quality control, streamlining the NGS data analysis journey. With both curated external and internal variant knowledgebases at hand, the automated variant interpretation feature accelerates CGH and NGS tertiary analysis efficiently. Alissa Interpret accommodates a variety of genomic variants, such as SNVs, InDels, CNVs, LOH, and fusions, all from a single platform. Additionally, its seamless integration with Laboratory Information Management Systems (LIMS) aids in removing bottlenecks in genomic data analysis. Interacting with peers fosters knowledge-sharing opportunities, which in turn enhances diagnostic accuracy and yields in clinical environments. This collaborative engagement not only promotes teamwork but also cultivates a community committed to the progression of genomic research and its applications, ultimately benefiting patient care.

Media

Media

Integrations Supported

Additional information not provided

Integrations Supported

Additional information not provided

API Availability

Has API

API Availability

Has API

Pricing Information

€100/month/seat
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

BioBam Bioinformatics S.L.

Date Founded

2011

Company Location

Spain

Company Website

www.biobam.com

Company Facts

Organization Name

Agilent Technologies

Date Founded

1999

Company Location

United States

Company Website

www.agilent.com/product/next-generation-sequencing/ngs-data-analysis-interpretation/alissa-interpret-4301560

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