Illumina Genomics Solutions
Discover Illumina's advanced genomics solutions including cutting-edge sequencing instruments and analysis software tailored for research and clinical applications.
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Description
Illumina offers a comprehensive suite of products and services designed for next-generation sequencing (NGS) and microarray applications. Key instruments include the MiSeq i100 Series, which provides rapid sequencing capabilities, and the NextSeq 1000/2000, known for their high throughput and quality output.
In addition to these instruments, Illumina provides a range of kits and reagents essential for sample preparation and library construction. The DRAGEN secondary analysis platform enhances data processing speed and accuracy, making it a valuable tool for large-scale genomic studies.
Illumina also features selection tools and software tailored for data analysis, streamlining workflows across various research domains such as cancer genomics, microbiology, and reproductive health. The integration of these tools facilitates efficient genomic research, enabling scientists to gain insights into complex biological questions.
With a focus on quality and speed, Illumina's solutions are pivotal for advancing genomic studies and clinical applications. The company's commitment to innovation continues to drive improvements in sequencing technologies and data analysis, supporting researchers and clinicians worldwide.
Features
MiSeq i100 Series
Compact sequencing instrument designed for rapid and high-quality sequencing, suitable for a variety of applications.
NextSeq 1000/2000
High-throughput sequencing systems that deliver fast and reliable data for large-scale genomic projects.
DRAGEN Secondary Analysis
A powerful analysis platform that accelerates genomic data processing with enhanced accuracy and efficiency.
Microarray Services
Comprehensive services for microarray applications, facilitating various research needs from discovery to validation.
Selection Tools and Software
A suite of tools designed to assist in assay design and workflow optimization for genomic research.
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Documentation & Support
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