2019
DOI: 10.1016/j.csbj.2019.07.008
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In-silico Design of DNA Oligonucleotides: Challenges and Approaches

Abstract: DNA oligonucleotides are essential components of a high number of technologies in molecular biology. The key event of each oligonucleotide-based assay is the specific binding between oligonucleotides and their target DNA. However, single-stranded DNA molecules also tend to bind to unintended targets or themselves. The probability of such unspecific binding increases with the complexity of an assay. Therefore, accurate data management and design workflows are necessary to optimize the in-silico … Show more

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Cited by 26 publications
(17 citation statements)
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References 76 publications
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“…Evaluating the specificity of the probe sequence through testing the DNA of various non-target organisms was also necessary. Finally, it is essential to optimize the hybridization conditions (Hendling and Barisic 2019).…”
Section: Discussionmentioning
confidence: 99%
“…Evaluating the specificity of the probe sequence through testing the DNA of various non-target organisms was also necessary. Finally, it is essential to optimize the hybridization conditions (Hendling and Barisic 2019).…”
Section: Discussionmentioning
confidence: 99%
“…It has been established as the optimal standard properties for a primer set, including primer size, product size, melting temperature, GC content, and binding energy [ 72 ]. The most important property is the thermodynamic parameter that guarantees the nonoccurrence of primer/probe dimerization for the designer.…”
Section: Influencing Factors On Sars-cov-2 Detectionmentioning
confidence: 99%
“…There are cost and performance implications for utilizing these large panels, as the number of probes required dictates the cost of probe synthesis (Briese et al, 2015 ; Wylie et al, 2015 ; Metsky et al, 2019 ). These assays tend to use shorter oligonucleotides as each additional nucleotide increases the uniqueness of an oligonucleotide by a factor of four (Hendling and Barišić, 2019 ). This design difference results in varying genome coverage, as large generic panels have a greater propensity to capture viral diversity but fewer whole genomes, whilst more targeted assays result in improved genome coverage but less viral diversity.…”
Section: Approachesmentioning
confidence: 99%