CLC bio and SciEngines Enable Real-Time Exact Alignment of NGS Data

8 Jul 2013

Product news

As a result of their ongoing partnership, CLC bio and SciEngines today announced integration between CLC bio's sequence analysis software and the newest model of SciEngines' FPGA-based RIVYERA computers. Instead of using heuristics, it is now possible to find exact matches between sequences at a speed of 11.5 trillion cell updates per second (CUPS) per server, approximately 3000x faster than a 3.0 GHz CPU thread.

Tim Pietruck, Vice President at SciEngines, states "In cases, where the scientist requires highest possible analysis quality but where ordinary computers are simply too slow, our RIVYERA architecture is opening up completely new possibilities. With the newest features in our Smith-Waterman implementation, the speed of the RIVYERA S6-LX150 and the intuitive usability of CLC bio's front-end, we're confident that exact sequence alignment approaches executed in real-time will start to play an increasing role in modern computational biology."

"In addition to the speed, we're confident our customers will gain tremendous value from the full-fledged feature set, including user-definable scoring matrices, support of affine gap penalties, reverse complement calculation, and mate-pair alignments." continues VP of Communications at CLC bio, Lasse Görlitz, and adds, "We're looking forward to see what compelling results our customers and partners potentially can achieve with this system!"

The combined solution is now available in a beta version, which will be demonstrated at the ISMB/ECCB conference in Berlin, Germany, July 21-23, 2013.

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DNA SequencingDNA sequencing, such as sanger sequencing, is a biological technique that determines the precise order of nucleotide bases in a fragment or template of DNA. DNA sequencers and genetic analyzers are based on capillary electrophoresis, where labeled DNA fragments are electrophoretically separated by size as they migrate through a polymer. Find the best DNA sequencing products, including DNA sequencing kits, genomic libraries and genetic identity kits in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.Next Generation SequencingNext-generation sequencing (NGS), also known as whole-genome sequencing, high-throughput sequencing and massive parallel sequencing, produces and analyses thousands to millions of nucleotide sequences at once. Sequencing systems operate via varying technologies depending on the manufacturer, including sequencing by synthesis, ligation, pyrosequencing, ion semiconductor and single-molecule real-time sequencing. For NGS, library preparation is paramount to successful sequencing. In this section, explore a range of library preparation kits, from targeted, amplicon-based or hybridization-based kits including epigenomic, transcriptomic and genomic workflows to fragmentation kits. Find the best next-generation sequencing products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.NGS SoftwareHigh ThroughputHigh throughput experiments allow the simultaneous processing of several samples. This parallelization reduces the cost per experiment and increases reproducibility and output volume of data.Sequence AlignmentSequencingSequencing refers to determining the order of nucleotides in a DNA or RNA molecule. This process is essential in genomics, diagnostics, and evolutionary biology. Techniques like next-generation sequencing (NGS) and Sanger sequencing provide high-throughput and precise data for analyzing genomes and transcriptomes. Browse our peer-reviewed product directory to find the best sequencing tools and reagents, compare products, check reviews, and get pricing directly from manufacturers.