Illumina Sequencing Platform
Analyzer IIx systems. Sequencing capabilities include both single-end sequencing (50 and 75bp read lengths) and pair-end sequencing (50, 75 and 100bp read lengths). Library construction for Illumina sequencing is available for whole genome, transcriptome (RNA-seq), exome, microRNA, and chromatin immunoprecipitation (ChIP), as well as for “bar coding” of samples for multiplex sequencing. The GSC has to date constructed nearly 2,000 libraries and generated over 5 trillion base pairs of data on the Illumina Genome Analyzer, contributing to many projects and publications.
Page last modified
Jun 25, 2010