DNA - Whole Genome
Resequencing
Illumina’s Genome Analyzer system’s powerful combination of read-length and paired-end flexibility enables the broadest range of genomic sequencing applications. Illumina’s robust sequencing chemistry supports a wide range of read lengths, allowing researchers to tailor each run to meet their needs. This platform supports de novo whole-genome sequencing and resequencing, SNP discovery, the identification of copy number variations and chromosomal rearrangements including deletions, insertions, and translocations.
Genome Analyzer Applications: DNA Sequencing