Applications

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, SNP discovery, identification of copy number variations, and chromosomal rearrangement.

• TruSeq DNA Sample Prep Kit
• TruSeq Exome Enrichment Kit
• Targeted Resequencing
• De Novo Sequencing
• Whole Human Genome Sequencing
• Sequencing Automation