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What is Partek Flow?

Partek bioinformatics software provides a comprehensive suite of statistical and visualization tools via an intuitive interface designed for researchers with varying levels of expertise. This innovative platform enables users to explore genomic data with remarkable speed and simplicity, effectively reflecting our slogan, "We turn data into discovery®." Featuring pre-configured workflows and pipelines in an easy-to-use point-and-click format, even intricate analyses of next-generation sequencing (NGS) and array data are made accessible to all researchers. Our unique blend of customized and publicly available statistical algorithms works seamlessly to convert NGS data into meaningful biological insights. The software’s engaging visual elements, such as genome browsers, Venn diagrams, and heat maps, reveal the complexities of next-generation sequencing and array data in striking detail. Furthermore, our dedicated team of Ph.D. scientists is always on hand to assist with any NGS analysis questions that may arise. Designed to accommodate the extensive computational demands of next-generation sequencing, the software also provides adaptable options for installation and user management, ensuring a well-rounded solution for diverse research objectives. Consequently, users can devote more of their time to advancing their research rather than grappling with technical obstacles, thereby enhancing productivity and discovery in their scientific endeavors.

What is Illumina DRAGEN Secondary Analysis?

The DRAGEN Secondary Analysis system from Illumina provides accurate, comprehensive, and exceptionally efficient processing of next-generation sequencing data. By leveraging a graph reference genome in combination with machine learning methodologies, it achieves outstanding precision. With a highly streamlined workflow, it can fully analyze a 34x whole human genome in roughly 30 minutes when operated on the DRAGEN server v4. Furthermore, it optimizes this process by reducing FASTQ file sizes by as much as five times. This system is proficient in handling diverse types of NGS data, such as whole genomes, exomes, methylomes, and transcriptomes. It has been designed to work seamlessly with the user's chosen platform and can scale to accommodate various needs. DRAGEN analysis is consistently recognized as a frontrunner in accuracy for detecting both germline and somatic variants, supported by its strong performance in industry competitions hosted by precisionFDA. This sophisticated analytical tool enables laboratories of all sizes and specialties to fully leverage their genomic datasets. Additionally, the integration of highly adaptable field-programmable gate array (FPGA) technology allows DRAGEN to implement hardware-accelerated genomic analysis algorithms, significantly improving its efficiency. These advancements firmly establish DRAGEN as an essential asset in the rapidly advancing realm of genomics, enabling researchers to push the boundaries of scientific discovery.

Media

Media

Integrations Supported

Integrations Supported

Amazon Web Services (AWS)
BaseSpace Sequence Hub
Correlation Engine
Emedgene
Illumina Connected Analytics

API Availability

API Availability

Has API

Pricing Information

Pricing not provided
Free Trial Offered?

Pricing Information

Pricing not provided
Free Trial Offered?

Supported Platforms

SaaS

Supported Platforms

SaaS
On-Prem

Customer Service / Support

24 Hour Support
Web-Based Support

Customer Service / Support

Standard Support
Web-Based Support

Training Options

Documentation Hub
Webinars
Online Training

Training Options

Documentation Hub
Webinars
Online Training
On-Site Training

Company Facts

Organization Name

Partek

Date Founded

2011

Company Location

United States

Company Website

www.partek.com

Company Facts

Organization Name

Illumina

Company Location

United States

Company Website

www.illumina.com/products/by-type/informatics-products/dragen-secondary-analysis.html

Categories and Features

Bioinformatics

Not specified

Life Sciences

Not specified

Categories and Features

Bioinformatics

Not specified

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