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The most affordable Illumina system, designed for everyday sequencing
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Prepare sequencing libraries from mRNA to get a clear view of the coding transcriptome with strand-specific information
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Mine over 20,000 genomic studies to get data-driven answers for genes, experiments, drugs and phenotypes for your research
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Verify instrument installation and operation, and obtain an audit-ready report
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Reagent kits for the NovaSeq 6000 System provide ready-to-use cartridge-based reagents for cluster generation and SBS
Low NovaSeq 6000 System sequencing costs spark new projects and customer growth
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Survey finds Americans unaware of DNA's power to improve lives
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Deep, comprehensive, and accessible sequencing power for detecting solid tumor biomarkers
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Local scientists analyze transmission patterns and trace origin of Ebola outbreak in the Democratic Republic of Congo
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A rapidly emerging method for studying biodiversity and monitoring ecosystem changes
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Families facing rare diseases often spend years pinpointing the problem in solitude – until now
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In podcast episode 41, Dr. Åke Borg discusses developing better biomarkers for risk stratification of individuals with breast cancer
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Rethink prenatal screenining. Think VeriSeq NIPT.
Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Perform transcriptome profiling for hundreds to tens of thousands of single cells in one experiment.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.
