(BUSINESS WIRE)–Mar. 4, 2015– Illumina, Inc. (NASDAQ:ILMN) announced the launch of TruSight® HLA, a complete, end-to-end solution that produces a comprehensive view of the HLA region by sequencing 11 HLA genes for accurate HLA typing across thousands of known and novel HLA alleles. Leveraging the MiSeq® Sequencing System, the kit includes the TruSight HLA Sequencing Panel, a single assay for ultra-high resolution analysis of all the key genes within the major histocompatibility complex (MHC), reagents for preparing and sequencing DNA libraries, and optimized data analysis with software from Conexio Genomics.
“Next-generation sequencing has great potential for HLA typing, but it has not been widely adopted beyond a few specialized laboratories,” said Matthew Anderson, M.D., Ph.D., Medical Director, BloodCenter of Wisconsin. “Our evaluation of TruSight HLA demonstrates the benefits that NGS technology can provide with a single, accurate, multi-locus assay that provides the resolution required to make confident HLA calls. TruSight HLA will enable more laboratories to harness the power of next-generation sequencing for HLA typing.”
HLA plays a large role in the body’s ability to recognize invasive cells and mount an immune response thus helping to fight disease and maintain overall health. This region of the genome is notoriously challenging to study due to high levels of sequence homology and dense variability. Currently the standard typing protocol requires 10 to 20 assays in two or three sequential rounds of testing to generate a high confidence HLA type with results based on about 6,500 base pairs of DNA sequence. TruSight HLA uses a single assay and generates results based on 65,000 base pairs, a ten-fold increase in sequence coverage, which significantly streamlines the workflow while greatly expanding the capacity to discover novel alleles.
TruSight HLA leverages Illumina sequencing by synthesis chemistry, the most trusted NGS technology. HLA typing researchers can use the solution to replace the multiple rounds of testing and the dozens of assays currently necessary to resolve ambiguous results. Through a streamlined workflow and multiplexed samples, this single assay and tightly integrated software enable labs to reduce hands-on time, decrease costs, improve productivity, and increase confidence in the results, while generating unambiguous, phase-resolved HLA typing results in less than four days.
“The HLA region of the genome plays a critical role in autoimmune disorders, cancer, transplant rejection, and drug sensitivity, but conventional technologies cannot efficiently sequence the region,” said Kirk Malloy, Senior Vice President and General Manager of Illumina’s Life Science Business. “By providing researchers with a reliable, faster, easier, more comprehensive method of HLA sequencing, TruSight HLA is one of many examples of how next-generation sequencing technologies fromIllumina can be applied to new markets where unlocking the power of the human genome holds great potential to make a positive difference in people’s lives.”
The TruSight HLA is now shipping. For more information, visit www.illumina.com/HLAseq.
Shares of Illumina closed yesterday at $196.03 . ILMN has a 1-year high of $213.33 and a 1-year low of $127.69. The stock’s 50-day moving average is $195.23 and it’s 200-day moving average is $183.52.
On the ratings front, Illumina has been the subject of a number of recent research reports. In a report issued on February 2, Cantor Fitzgerald analyst Sung Ji Nam maintained a Hold rating on ILMN, with a price target of $166, which implies a downside of 15.3% from current levels. Separately, on January 28, Maxim Group’s Bryan Brokmeier reiterated a Buy rating on the stock and has a price target of $255.
In total, one research analyst has assigned a Hold rating and 6 research analysts have given a Buy rating to the stock. When considering if perhaps the stock is under or overvalued, the average price target is $196.03 which is 18.3% above where the stock closed yesterday.
Illumina Inc providessequencing-and array-based solutions for genetic analysis. Itsproducts enabled researchers to explore DNA, helping them create the first map of gene variations associated with health, disease, and drug response.