精选研究人员

精选文献

• Next is now: new technologies for sequencing of genomes, transcriptomes, and beyond. Lister R et al. 2009.
• Genomic copy number variation, human health, and disease. Wain LV et al. 2009.

精选伙伴

iGenix, Inc. provides Illumina BeadXpress lab services for genotyping, copy number variation assessment, methylation and expression studies, maximizing your research efficiency and data accuracy.

新闻与事件

• American Society of Human Genetics (ASHG) November 2-6, Washington D.C.
• Illumina Receives FDA 510(k) Clearance for Its BeadXpress(R) Multiplex Analysis System
• Illumina Now Shipping HiScan(TM)SQ Platform
• Illumina Announces Its First Full Coverage DNA Sequencing of a Named Family