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Last updated on April 19, 2014 at 5:20 EDT

New Breakthrough Ion AmpliSeq(TM) Technology Delivers the Most Rapid and Comprehensive Sequencing of Gene Mutations to Advance Clinical Research

June 5, 2012

CARLSBAD, Calif., June 5, 2012 /PRNewswire/ — Life Technologies Corporation (NASDAQ: LIFE) today announced an expanded Ion AmpliSeq((TM)) product line with the launch of new breakthrough Comprehensive Cancer and Inherited Disease Panels. These first of kind panels, when coupled with Ion AmpliSeq(TM) Designer V1.2, Ion AmpliSeq(TM) Library Kit 2.0 and the new Ion Reporter(TM) Software, represent complete solutions for scientists researching the genetic basis of human diseases.

Sequencing the millions of cancer research samples stored in bio-repositories around the world is a primary unmet need of the cancer research community. Analyzing these samples using next generation sequencing (NGS) has been difficult, as typically only nanogram amounts of DNA can be isolated, far less than current commercial protocols require. In addition, NGS creates a flood of data, requiring expensive bioinformatics expertise to interpret. The latest set of Ion AmpliSeq(TM) and Ion Reporter(TM) products from Ion Torrent offer turn-key solutions to overcome these challenges.

Bringing Simplicity and Speed to Disease Research Workflows

Ion AmpliSeq(TM) Panels, whether predesigned and therefore ready-to-use, or custom built to probe specific genes of interest, deliver a simplified, single day workflow comprising target selection, amplification, sequencing and analysis. Further, when using Ion Reporter(TM) Software, the integrated workflow also includes annotated readout detailing the biological significance of observed gene mutations. The breakthrough Ion AmpliSeq(TM) technology requires only tens of nanograms of input DNA, compared to technologies offered by other companies that require hundreds of nanograms or even micrograms of starting material. Orthogonal confirmation of variants observed with Ion AmpliSeq(TM) Panels is readily accomplished by selecting from 4.5 million ready-to-use TaqMan® SNP Genotyping assays or by designing a custom TaqMan® assay. TaqMan® assays deliver “gold standard” sensitivity and specificity for SNP genotyping, and they may be analyzed in standard or digital PCR mode if increased sensitivity is required to detect low frequency or somatic mutations.

Scalability Demonstrated With Latest Edition of Ion AmpliSeq(TM) Designer Software

Initially launched in March, Ion AmpliSeq(TM) Designer has been immediately adopted by researchers world-wide, with over 1,000 custom designs submitted since inception. Ion AmpliSeq(TM) Designer Version 1.2 provides an additional leap in performance by generating up to 3,072 amplicons in a single tube – allowing capture of up to 1 Mb of genetic sequence. This high level of multiplexing streamlines the workflow by ensuring that only 1 or 2 primer pools are needed for custom designs and also reduces the amount of input DNA required for analysis. Ion AmpliSeq(TM) Designer delivers exceptional performance, with target design rates and coverage uniformity up to 98%.

Improved Performance of Ion AmpliSeq(TM) Cancer Panel

In October of 2011 Ion Torrent launched the Ion AmpliSeq(TM) Cancer Panel, which has quickly become the product of choice for scientists working to advance clinical cancer research. Now, by pairing this 46 gene cancer hot spot panel with the new Ion AmpliSeq Library Kit 2.0, scientists can detect rare somatic mutations and enjoy 98% coverage uniformity and further reductions in strand bias.

New Ion AmpliSeq(TM) Comprehensive Cancer Panel

With input from leading cancer research institutions, the Ion AmpliSeq(TM) Comprehensive Cancer Panel (CCP) reveals tumor mutation profiles and is optimized for use with formalin fixed paraffin embedded, (FFPE) tissues. This panel allows sensitive, high coverage detection of rare genetic variants by employing more than 16,000 primer pairs targeting over 400 genes involved in tumor formation. Compared to whole exome sequencing, Ion AmpliSeq(TM) CCP requires only 40 ng of input DNA, has a significantly lower price, and provides nearly 10-fold better coverage of individual genes, providing better sensitivity and specificity to detect somatic mutations. The Ion AmpliSeq(TM) Comprehensive Cancer Panel delivers exceptional quality, with coverage uniformity and on target bases both greater than 90%.

“The Comprehensive Cancer Panel and Ion Reporter will allow us to quickly survey samples in our bio-repositories and understand the signatures of different cancer types,” stated Dr. Marilyn Li, Professor in the Department of Molecular and Human Genetics and Director of the Cancer Genetics Lab at Baylor College of Medicine. Dr. Li added, “This will enable us to tackle key issues in cancer research: to define the nature and understand the pathologic behavior of cancer cells and to identify biomarkers that could help in the future to diagnose cancers at an early, curable stage or to optimize therapy for individual patients.”

The Ion AmpliSeq(TM) Comprehensive Cancer Panel can be paired with the Ion AmpliSeq(TM) Cancer Panel or Ion AmpliSeq(TM) Designer (www.ampliseq.com), to generate focused custom panels for any human gene targets.

New Ion AmpliSeq(TM) Inherited Disease Panel

Also launched today, the Ion AmpliSeq(TM) Inherited Disease Panel, (IDP) comprehensively targets 328 genes associated with 176 common Mendelian diseases, while accommodating analysis of compromised or degraded samples containing low input DNA. The new panel was designed in consultation with clinical molecular geneticists researching inherited diseases, and enables detection of both known and de novo mutations. The Ion AmpliSeq(TM) Inherited Disease Panel delivers exceptional quality, with coverage uniformity and on target bases both greater than 90%.

Removing Bioinformatics Barriers with Ion Reporter(TM) Software

The Ion Reporter(TM) Software is a first of its kind application that eliminates expensive and complex bioinformatics barriers, allowing rapid and simple identification and annotation of mutations to advance clinical research. The secure cloud-based software performs alignments, generates variants, and performs automated annotation on Ion PGM(TM) data, revealing biological significance. Variants are classified into simple categories that are summarized into a report, allowing easier interpretation by researchers unfamiliar with sequencing. Ion Reporter(TM) Software offers customizable workflows for multiple linked samples, enabling reproducible analysis for routine assays and sharing of Ion AmpliSeq(TM) experiments across a geographically dispersed set of users, thereby accelerating team based research. Ion Reporter(TM) Software will catalyze new and exciting clinical research applications developed by both Life Technologies and other external partners. With Ion Reporter(TM) Software, researchers no longer need to invest in large expensive computing infrastructure and instead can benefit from the scalability of cloud computing.

All above mentioned products are For Research Use Only, Not for use in diagnostic procedures.

About Life Technologies

Life Technologies Corporation (NASDAQ: LIFE) is a global biotechnology company with customers in more than 160 countries using its innovative solutions to solve some of today’s most difficult scientific challenges. Quality and innovation are accessible to every lab with its reliable and easy-to-use solutions spanning the biological spectrum with more than 50,000 products for translational research, molecular medicine and diagnostics, stem cell-based therapies, forensics, food safety and animal health. Its systems, reagents and consumables represent some of the most cited brands in scientific research including: Ion Torrent(TM), Applied Biosystems®, Invitrogen(TM), GIBCO®, Ambion®, Molecular Probes®, Novex®, and TaqMan®. Life Technologies employs approximately 10,400 people and upholds its ongoing commitment to innovation with more than 4,000 patents and exclusive licenses. LIFE had sales of $3.7 billion in 2011. Visit us at our website: http://www.lifetechnologies.com.

Life Technologies’ Safe Harbor Statement

This press release includes forward-looking statements about our anticipated results that involve risks and uncertainties. Some of the information contained in this press release, including, but not limited to, statements as to industry trends and Life Technologies’ plans, objectives, expectations and strategy for its business, contains forward-looking statements that are subject to risks and uncertainties that could cause actual results or events to differ materially from those expressed or implied by such forward-looking statements. Any statements that are not statements of historical fact are forward-looking statements. When used, the words “believe,” “plan,” “intend,” “anticipate,” “target,” “estimate,” “expect” and the like, and/or future tense or conditional constructions (“will,” “may,” “could,” “should,” etc.), or similar expressions, identify certain of these forward-looking statements. Important factors which could cause actual results to differ materially from those in the forward-looking statements are detailed in filings made by Life Technologies with the Securities and Exchange Commission. Life Technologies undertakes no obligation to update or revise any such forward-looking statements to reflect subsequent events or circumstances.

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Life Technologies Contact
Wes Conard
415-385-4455
Wes.Conard@lifetech.com

SOURCE Life Technologies


Source: PR Newswire