Agilent Technologies Inc. (NYSE: A) has announced it is collaborating with Baylor College of Medicine’s Medical Genetics Laboratories to provide customized CGH (comparative genomics hybridization) microarrays to researchers worldwide. Six new microarray designs unite the power of Baylor’s data-rich expertise in genetics research with Agilent’s microarray manufacturing capabilities to enable advanced discoveries in cancer and cytogenetics research. The collaboration announcement was delivered at the American Society of Human Genetics conference in Boston last month. “Designing arrays of this complexity has been an enormous effort at Baylor College of Medicine, and we are excited to partner with Agilent to share the designs with laboratories in the U.S. and internationally,” said T. Brandon Perthuis, director of business development at the BCM Medical Genetic Laboratories. “Originally focused on micro-deletions and micro-duplications, our current designs have been continually improved over the past 10 years and are now highly robust, with the ability to detect exon-level deletions and duplications,” he said. “Our exon array targets approximately 1,700 genes and includes probes used for SNP analysis for the detection of AOH and UPD [absence of heterozygosity and uniparental disomy].” “After years of intense study, we are proud to join with Baylor—a global leader in cancer and cytogenetics research—to provide researchers with these powerful new tools for disease research,” said Jacob Thaysen, vice president and general manager for Agilent’s Diagnostics and Genomics business. Agilent manufactures a broad selection of microarrays for genome-wide measurement of gene expression and for comparative genomics hybridization, as well as SureFISH, a highly specific and sensitive product line for oligonucleotide fluorescent in situ hybridization. The company’s human genome CGH microarrays are available in multiple formats with bundling options available. About the Medical Genetics Laboratories at Baylor College of Medicine For over 40 years, the Medical Genetics Laboratories at Baylor College of Medicine has been dedicated to providing the medical genetics community with comprehensive research and genetic testing services relevant to twenty-first century medicine. About Agilent in Genomics Agilent Technologies Inc. is a global leader in target enrichment for next-generation sequencing and genomic microarrays. The Agilent SureSelect and HaloPlex target enrichment systems enable researchers to easily choose which segments of a genome to sequence, avoiding the time and expense needed to sequence the entire genome. HaloPlex offers a same-day sample-to-sequencer workflow; SureSelect can accurately capture whole exomes and whole methylomes in a single reaction. These are just two products arising from Agilent’s expertise in synthesizing custom complex mixtures of long oligonucleotides gained in microarray manufacturing. Additional product lines built on this core technology include microarrays for genome-wide measurement of gene expression and for comparative genomics hybridization, as well as SureFISH, a highly specific and sensitive product line for oligonucleotide fluorescent in situ hybridization. In addition to oligonucleotide-based products, Agilent offers a microfluidic bioanlyzer to measure sample quality, and a full set of reagents, hardware, methods and bioinformatics software for genomic experiments.
About Agilent TechnologiesAgilent Technologies Inc. (NYSE: A) is the world’s premier measurement company and a technology leader in chemical analysis, life sciences, diagnostics, electronics and communications. The company’s 20,500 employees serve customers in more than 100 countries. Agilent had revenues of $6.9 billion in fiscal 2012. Information about Agilent is available at www.agilent.com. NOTE TO EDITORS: Further technology, corporate citizenship and executive news is available at www.agilent.com/go/news.