ABI SOLiD Next Generation Sequencer

The SOLiD System is a highly accurate, massively parallel next-generation sequencing platform that supports a wide range of applications. The flexibility of two independent flow cells and multiplexing capability allow you to conduct multiple experiments in a single run. With unparalleled throughput and greater than 99.94% basecalling accuracy, the SOLiD System enables you to complete large-scale sequencing and tag experiments more cost effectively than previously possible

Scalable 

The SOLiD System open slide format and flexible bead densities enable increases in throughput with modest analysis, protocol and chemistry optimizations. While competitive technologies are already near maximum throughput, the SOLiD System is scalable to meet your research needs today and tomorrow utilizing the same platform.

Accurate

accuracy greater than 99.94%, due to 2 base encoding, the SOLiD System distinguishes itself by providing data that is significantly more accurate than alternative next-generation platforms for variation detection. 2 Base encoding enables unique error checking capability, providing higher confidence in each call. With the SOLiD System, scientists can focus on the biological significance of their results rather than sifting through poor quality data.

Ultra High Throughput 

The SOLiD 3 Plus System generates 60+ gigabases and >1 billion tags per run,which is more usable data than any other next-generation system available today. This level of throughput enables large scale resequencing and tag based experiments to be completed more cost effectively than ever before.

Flexible

The independent flow cell configuration of the SOLID Analyzer enables you to run two completely independent experiments in a single run ssentially providing 2 instruments in one. The combination of multiple slide configuration and sample multiplexing capability enables you to cost-effectively analyze multiple samples cost effectively for a variety of applications.

Mate Pairs

System supports sample preparation for mate-paired libraries with insert sizes ranging from 600 bp up to 10 kbp. This broad range of insert sizes combined with ultra high throughput and flexible 2 flow cell configuration enables more precise characterization of structural variation across the genome.