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What is Universal Analysis Software (UAS)?

Universal Analysis Software (UAS) serves as a versatile platform designed to streamline the analysis and management of forensic genomic data, simplifying complex bioinformatics challenges for its users. This powerful software includes a diverse range of analysis modules that seamlessly integrate with various ForenSeq workflows, including ForenSeq MainstAY, ForenSeq Kintelligence, ForenSeq DNA Signature Prep, ForenSeq mtDNA Whole Genome, and ForenSeq mtDNA Control Region. By utilizing UAS, users can quickly produce FASTQ files, perform alignment tasks, and detect forensically relevant variants from next-generation sequencing (NGS) datasets. The software's rigorous validation processes ensure reliable variant identification, delivering accurate results in a user-friendly format without the hassle of per-seat licensing costs. Specifically crafted for forensic analysts, UAS enhances the management of detailed sequence data, providing a comprehensive suite of functionalities that facilitate the effective review of standard STR profiles and allow for thorough examination of even the most complicated samples. Furthermore, this adaptability contributes significantly to improving the efficiency and effectiveness of forensic investigations across various scenarios.

What is Galaxy?

Galaxy is an open-source, web-oriented platform tailored for managing data-rich research within the biomedical sector. New users are encouraged to start with the basic introductory resources or seek out the extensive help options available to them. Additionally, it is possible to establish a personal instance of Galaxy by following a comprehensive tutorial while choosing from a broad selection of tools provided in the tool shed. The current operational Galaxy instance benefits from the infrastructure offered by the Texas Advanced Computing Center. Moreover, further resources can be accessed through the Jetstream2 cloud, which is enabled by ACCESS and backed by the National Science Foundation. Researchers have the ability to quantify, visualize, and summarize discrepancies found in deep sequencing datasets while also constructing maximum-likelihood phylogenetic trees. The platform also facilitates phylogenomic and evolutionary tree construction with multiple sequences, enables the clustering of matching reads using the TN-93 method, and allows for the exclusion of sequences from a reference within a designated distance of a cluster. Additionally, researchers can perform maximum-likelihood estimations to determine gene essentiality scores, reinforcing Galaxy's status as an invaluable instrument for diverse genomic research applications. With its robust capabilities and user-friendly design, Galaxy continues to advance the frontiers of biomedical research.

Media

Media

Integrations Supported

Integrations Supported

Arch
CoinRoutes
Inn-Flow
Lybra Assistant

API Availability

API Availability

Has API

Pricing Information

Pricing not provided

Pricing Information

Free
Free Version

Supported Platforms

Windows

Supported Platforms

SaaS

Customer Service / Support

Standard Support
Web-Based Support

Customer Service / Support

Web-Based Support

Training Options

Documentation Hub
On-Site Training

Training Options

Documentation Hub

Company Facts

Organization Name

Verogen

Date Founded

2017

Company Location

United States

Company Website

verogen.com/products/universal-analysis-software/

Company Facts

Organization Name

Galaxy

Company Location

United States

Company Website

usegalaxy.org

Categories and Features

Bioinformatics

Not specified

Medical Lab

Data Analysis Auditing
Lab Instrument Interface
Sample Tracking

Categories and Features

Bioinformatics

Not specified

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