Abstract
The development of multiplex polymerase chain reaction and microarray assays is challenging due to primer dimer formation, unspecific hybridization events, the generation of unspecific by-products, primer depletion, and thus lower amplification efficiencies. We have developed a software workflow with three underlying algorithms that differ in their use case and specificity, allowing the complete in silico evaluation of such assays on user-derived data sets. We experimentally evaluated the method for the prediction of oligonucleotide hybridization events including resulting products and probes, self-dimers, cross-dimers and hairpins at different experimental conditions. The developed method allows explaining the observed artefacts through in silico WGS data and thermodynamic predictions. PRIMEval is available publicly at https://primeval.ait.ac.at.
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CITATION STYLE
Conzemius, R., Hendling, M., Pabinger, S., & Barišić, I. (2019). PRIMEval: Optimization and screening of multiplex oligonucleotide assays. Scientific Reports, 9(1). https://doi.org/10.1038/s41598-019-55883-4
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