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Rubicon Genomics, Inc. Launches Picoplex™ DNA-SEQ For Illumina, Inc. (ILMN) NGS Platforms


2/10/2014 9:43:00 AM

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Ann Arbor, MI – February 10, 2014 – Rubicon Genomics, Inc. today announced the launch of its PicoPLEX™ DNA-seq Kits for use with Illumina next-generation sequencing (NGS) platforms. PicoPLEX’s outstanding robustness and reproducibility have made it the worldwide standard for single-cell DNA amplification for microarray and PCR-based pre-implantation genetic screening and diagnosis. PicoPLEX DNA-seq now enables researchers and clinicians to access PicoPLEX technology for analyses conducted on Illumina NGS systems.

PicoPLEX DNA-seq employs the same technology currently used by IVF clinics to detect chromosomal aneuploidies, copy number variations and single-gene disorders in reproductive cells. It is also used for the genetic characterization of other single-cell samples such as circulating tumor cells. The easy-to-use, three-step process is performed in a single tube or well in less than three hours, thereby reducing error and contamination, speeding time to results and reducing costs.

James Koziarz, PhD, CEO of Rubicon Genomics, commented, “PicoPLEX DNA-seq emphasizes our commitment to increasing the robustness and reproducibility of DNA analyses while also delivering greater speed, efficiency and cost savings. This launch represents another milestone in our ongoing strategy to make Rubicon Genomics’ proprietary library preparation technology available to users of all sequencing platforms.”

PicoPLEX DNA-seq Kits amplify DNA to yield a highly reproducible NGS-ready library from a single cell with input concentrations of six picograms or less.

Dr. Brian Mariani, Chief Scientist and Scientific Director of the Genetics and IVF Institute, helped test the PicoPLEX DNA-seq Kits. He commented, “Remarkably, the sequencing data from the PicoPLEX DNA-seq libraries of embryo DNA clearly identified a male balanced translocation that had not been detected by previous microarray and FISH analyses. This is a significant example of how PicoPLEX sequencing data can expose important structural rearrangements missed by other approaches.”

At the 15th Annual Advances in Genome Biology and Technology (AGBT) meeting, Rubicon CSO Dr. John Langmore will discuss "Pre-implantation genetic screening and diagnostics (PGS/PGD) at low NGS coverage for aneuploidy, CNV, and single-gene disorder detection for in vitro fertilization.” AGBT 2014 will be held on Marco Island, Florida, February 12-15, 2014. For more information, visit www.agbt.org/about.html.

For more information on PicoPLEX DNA-seq, visit http://rubicongenomics.com/products/picoplex-dna-seq-kit.

Join Rubicon for a free webinar, “PicoPLEXTM DNA-seq: Single Cell Sequencing, Theory and Applications,” featuring Jeremiah Smith, PhD, of the University of Kentucky, on February 19, 2014 at 10:00am ET. For more information, click here.

About Rubicon Genomics
Rubicon Genomics, Inc. is a leader in the development and commercialization of innovative sample-specific nucleic acid library preparation products used in research and clinical testing on NGS, microarray and q-PCR platforms. The company creates efficient molecular biology tools for genetic, epigenetic and expression analysis of difficult samples to facilitate gene-based research, drug development and diagnostics. Privately-held Rubicon is located in Ann Arbor, Michigan. For more information, visit rubicongenomics.com.

Barbara Lindheim
BLL Partners, LLC
blindheim@bllbiopartners.com
1370 Broadway, 5th floor
New York, NY 10018
212.584.2276 (office)
917.355-9234 (mobile)

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