| Literature DB >> 31991148 |
Christoph Kreer1, Matthias Döring2, Nathalie Lehnen3, Meryem S Ercanoglu1, Lutz Gieselmann1, Domnica Luca1, Kanika Jain1, Philipp Schommers4, Nico Pfeifer5, Florian Klein6.
Abstract
To study the diversity of immune receptors and pathogens, multiplex PCR has become a central approach in research and diagnostics. However, insufficient primer design against highly diverse templates often prevents amplification and therefore limits the correct understanding of biological processes. Here, we present openPrimeR, an R-based tool for evaluating and designing multiplex PCR primers. openPrimeR provides a functional and intuitive interface and uses either a greedy algorithm or an integer linear program to compute the minimal set of primers that performs full target coverage. As proof of concept, we used openPrimeR to find optimal primer sets for the amplification of highly mutated immunoglobulins. Comprehensive analyses on specifically generated immunoglobulin variable gene segment libraries resulted in the composition of highly effective primer sets (oPR-IGHV, oPR-IGKV and oPR-IGLV) that demonstrated to be particularly suitable for the isolation of novel human antibodies.Entities:
Year: 2020 PMID: 31991148 DOI: 10.1016/j.jim.2020.112752
Source DB: PubMed Journal: J Immunol Methods ISSN: 0022-1759 Impact factor: 2.303