Multiplex PCR Primer Design Software
Visual OMP™ (Multiplex PCR primer design software) makes it easy to design sets of primers and probes optimized to work under your experimental conditions.
Design primer pairs and probe sets in any combination, even in the presence of your existing oligo sets. Once you indicate the details of your experiment, Visual OMP™ has powerful design algorithms which use the nearest-neighbor model and coupled multi-state equilibrium models to simulate thousands of possible combinations in order to identify the most selective and sensitive oligo solution sets.
Multistate Coupled Equilibrium Model
Specify a target, choose a design type, and define experiment conditions and Visual OMP’s design engine will automatically determine the most stable and specific PCR primer design for your single- or multiplexed assay.
Visual OMP’s simulation engine allows for the input and thermodynamic analysis of existing primers in the presence of newly designed primers in a molecular simulation.
Visual OMP will optimize beacon probe and stem length design for a given set of experimental conditions to ensure that free beacons form hairpins to quench fluorescence, while selectively bound beacons fluoresce. Beacons can also be simulated using a variety of flurophore and quencher pairs to optimize your assay.
Sensitivity can be a huge factor when designing for SNPs due to cross-hybridization which may lead to false positives. Visual OMPs design engine can design allele-specific primers and probes to optimize polymorphism detection sensitivity.
Visual OMP provides a ranked set of highly specific multiplex PCR primer designs which do not cross-hybridize or form primer dimers.
Visual OMP can design highly selective Taqman probe sequences that can be simulated to exhibit the thermodynamic effects of fluorophores, quenchers and minor groove binders to DNA duplex stability.
False positives and negatives can be avoided by utilizing Visual OMP to increase the quality and performance of DNA probes while simultaneously avoiding cross-hybridization and mishybridization.
Fast and accurate simulated folding under a variety of salt and temperature profiles simplifies RNA target accessibility and complexity to optimize primer and probe design.