At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. for Rare Pediatric Diseases, Rare A high-performing, fast, and integrated workflow for sensitive applications such as human whole-genome sequencing, Bringing efficiency and high confidence to case management, variant analysis, and interpretation in rare disease, Fast, high-quality, sample-to-data services such as RNA and whole-genome sequencing, Find popular product groupings for your workflow, Enables and accelerates research leveraging BaseSpace Correlation Engine, Environmentally friendly packaging reduces waste from landfills and carbon emissions, Three approaches to help researchers with sequencing, Expanded portfolio enables comprehensive genomic profiling from blood and tissue, This high-throughput NGS test detects SARS-CoV-2 in nasopharyngeal, oropharyngeal, and mid-turbinate nasal swabs, A transformational approach to biodiversity monitoring, New library prep kits enhance research in rare genetic diseases, All Terms and Conditions | Illumina innovative sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. © 2020 Illumina, Inc. All rights reserved. Illumina is headquartered in San Diego, CA and has 17 office locations across 10 countries. Button navigates to Illumina Europe offices page. for Illumina Cancer Hotspot Panel v2, AmpliSeq For Research Use Only. Genomics Changed Herd Management, Large-Scale As a global company that places high value on collaborative interactions, rapid delivery of solutions, and providing the highest level of quality, we strive to meet this challenge. You can sign up for additional alert options at any time. Our mission is everything to us. Host: https://www.illumina.com | As a global leader in genomics, our sequencing and array technologies are fueling groundbreaking advancements in life science research, translational and consumer genomics, and molecular diagnostics. into Recurrent Pregnancy Loss, Education Custom Assay Designer, Instrument Catalyze Patient Access to Genomic Testing, Patients Not for use in diagnostic procedures (except as specifically noted). Tax Reg: 105-87-87282 | Whole-Genome Sequencing, Microbiome Methyl Capture EPIC Library Prep Kit, SureCell After submitting your request, you will receive an activation email to the requested email address. If you experience any issues with this process, please contact us for further assistance.

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