Illumina's sequencers powerfully combine the flexibility of single reads, short- and long-insert paired-end reads, enabling the broadest range of genomic applications. TruSeq sequencing chemistry supports this wide range of applications including whole-genome sequencing, targeted resequencing, de novo sequencing, amplicon sequencing, SNP discovery, identification of copy number variations, and chromosomal rearrangement. Nextera technology enables researchers to accelerate sample preparation and produce sequencing-ready libraries in less than 90 minutes.

Next-Gen Sequencing and Microarrays
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Expand the power of your study—next-gen sequencing and arrays.

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