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Announcing NextSeq 1000 and NextSeq 2000.
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The power of high-throughput sequencing on a benchtop system with the v2.5 flow cell for greater stability and robustness
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Prepare sequencing libraries for small genomes, PCR amplicons, plasmids, or cDNA in as little as 90 minutes
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Accurate, rapid analysis for germline and somatic exome experiments
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Verify instrument installation and operation, obtain an audit-ready report
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Generating RNA libraries from ultra-low-input samples
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By Dr Phil Febbo, Chief Medical Officer at Illumina
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Assay targeting multiple variant types, including tumor mutational burden (TMB) and microsatellite instability (MSI), even from low-quality samples.
Cost-efficient flexibility for new and emerging applications.
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.
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