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Illumina

Illumina develops, manufactures and markets integrated systems for the analysis of genetic variations and biological functions. The company also provides sequencing and array-based solutions for genetic analysis, as well as genotyping, NIPT and whole-genome sequencing services for government laboratories, hospitals, an ...
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Covid-19 Illumina

Clinical Laboratory

SARS-CoV-2 NGS Test
Illumina COVIDSeq Test

The Illumina COVIDSeq Test is a high-throughput, next-generation sequencing test is intended for the detection of SARS-CoV-2 virus RNA in authorized countries and virus genome analysis for research use. This amplicon-based NGS test includes 2019-nCoV primers designed to detect RNA from the SARS-CoV-2 virus in nasopharyngeal, oropharyngeal, and mid-turbinate nasal swabs from patients with signs and symptoms of infection who are suspected of COVID-19.
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SARS-CoV-2 (COVID-19) Test
Illumina COVIDSeq Test

The Illumina COVIDSeq Test is the first NGS test approved for use under the US Food and Drug Administration’s Emergency Use Authorization (EUA). This amplicon-based NGS test includes 2019-nCoV primers designed to detect RNA from the SARS-CoV-2 virus in nasopharyngeal, oropharyngeal, and mid-turbinate nasal swabs from patients with signs and symptoms of infection who are suspected of COVID-19. The test can be run on the Illumina NovaSeq 6000 Sequencing System, NextSeq 500 Sequencing System, NextSeq 550 Sequencing System, or NextSeq 550Dx Instrument.
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News of Illumina

Illumina Acquires GRAIL to Accelerate Patient Access to Life-Saving Multi-Cancer Early-Detection Test

20 Aug 2021
Illumina Acquires GRAIL to Accelerate Patient Access to Life-Saving Multi-Cancer Early-Detection Test
Illumina, Inc. (San Diego, CA, USA) has acquired GRAIL (Menlo Park, CA, USA), a healthcare company focused on life-saving early detection of multiple cancers.
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About Illumina

Illumina develops, manufactures and markets integrated systems for the analysis of genetic variations and biological functions. The company also provides sequencing and array-based solutions for genetic analysis, as well as genotyping, NIPT and whole-genome sequencing services for government laboratories, hospitals, and reference laboratories, among others.
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Sequencing System

Sequencing System

Model: NovaSeq 6000 Sequencing System
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Description:

The NovaSeq 6000 Sequencing System performs whole-genome sequencing more efficiently and cost-effectively than ever. Its scalable output generates up to 6 Tb and 20 billion reads in dual flow cell mode with simple streamlined automated workflows. The system can be configured to sequence a trio in one day or up to 48 genomes in ~2 days for the most comprehensive coverage.

Tags: [Clinical Laboratory], [General Lab]
Features Specifications

Features

• Scalable throughput for studies of all sizes
• Broad, deep sequencing for bigger discoveries
• Flexible performance for mix and match options
• Streamlined operations for increased efficiency Request Information

Specifications

Instrument configuration
• Computer and touch screen display
• Installation setup and accessories
• Data collection and analysis software

Instrument control computer
• Base Unit: Portwell WADE-8022 with Intel i7 4700EQ CPU
• Memory: 2 × 8 GB DDR3L SODIMM
• Hard Drive: None
• Solid-State Drive: 256 GB mSATA
• Operating System: Windows 10
Note: Computer configurations will be upgraded regularly; contact your local account manager for current configuration

Operating environment
• Temperature: 19°C-25°C (22°C ±3°C), Request Information

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