HOUSTON, April 14 /PRNewswire/ -- SeqWright Inc., a leading Genomics CRO, has added 454's GS FLX(TM) system to increase the breadth of its next generation offerings and to provide genomic researchers with more cost effective genomics solutions. The GS FLX(TM) system will complement SeqWright's current ABI SOLiD(TM) platform and enable the company to offer a more diverse array of next generation services, including de novo sequencing of higher organisms. This dual-system model is designed to make genomics projects of any size and scope accessible to vastly more researchers and thereby, increase the pace of genomics research.
The addition of the GS FLX(TM) system brings with it a ten fold increase in sequence read-length compared to other next generation platforms; reads which approach those of Sanger-based technologies. The increased read length of the GS FLX(TM) system is the primary factor behind SeqWright's capability of offering de novo sequencing of higher organisms and the system's greatest advantage over competitive platforms.
The capacity of SeqWright to provide cost effective genomic solutions for virtually any genomics project stems from the synergy created by the combination of the GS FLX(TM) with the company's existing SOLiD(TM) platform. The long read lengths of the GS FLX(TM) combined with the extremely high throughput of SOLiD(TM) are a perfect complement to each other. For example, utilizing the strengths of the two systems, SeqWright can create a scaffold sequence using the long reads of the GS FLX(TM) and subsequently combine that scaffold with the vast amounts of sequence data from SOLiD(TM) to build up the genomic coverage. When compared to Sanger-based methods, the decrease in cost and the increase in speed of SeqWright's dual-system, next generation, approach is remarkable.
SeqWright Senior VP, David Buck, Ph.D., remarked this regarding
SeqWright's recent acquisition, "The 454 platform is quite a natural
addition to o
|SOURCE SeqWright Incorporated|
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