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  2. Netprimer - Wikipedia

    en.wikipedia.org/wiki/Netprimer

    NetPrimer is a gratis web-based tool used for analysing primers used in PCR to amplify a DNA sequence. [2] The software predicts the melting temperature of the primers using the nearest neighbor thermodynamic algorithm. The accurate prediction of the melting temperature (Tm) is one of the most important factors that governs the success of a PCR ...

  3. Melting curve analysis - Wikipedia

    en.wikipedia.org/wiki/Melting_curve_analysis

    Melting curve analysis is an assessment of the dissociation characteristics of double-stranded DNA during heating. As the temperature is raised, the double strand begins to dissociate leading to a rise in the absorbance intensity, hyperchromicity. The temperature at which 50% of DNA is denatured is known as the melting temperature. Measurement ...

  4. Nucleic acid thermodynamics - Wikipedia

    en.wikipedia.org/wiki/Nucleic_acid_thermodynamics

    Nucleic acid thermodynamics is the study of how temperature affects the nucleic acid structure of double-stranded DNA (dsDNA). The melting temperature (T m) is defined as the temperature at which half of the DNA strands are in the random coil or single-stranded (ssDNA) state. T m depends on the length of the DNA molecule and its specific ...

  5. In silico PCR - Wikipedia

    en.wikipedia.org/wiki/In_silico_PCR

    It is fast (through use of a genome's FM-index) and can account for primer melting temperature and tolerated edit distances between primers and hit locations on the genome. VPCR [ 3 ] runs a dynamic simulation of multiplex PCR, allowing for an estimate of quantitative competition effects between multiple amplicons in one reaction.

  6. COLD-PCR - Wikipedia

    en.wikipedia.org/wiki/COLD-PCR

    The underlying principle of COLD-PCR is that single nucleotide mismatches will slightly alter the melting temperature (Tm) of the double-stranded DNA. Depending on the sequence context and position of the mismatch, Tm changes of 0.2–1.5 °C (0.36–2.7 °F) are common for sequences up to 200bp or higher.

  7. High-resolution melting analysis - Wikipedia

    en.wikipedia.org/wiki/High-resolution_melting...

    In addition to typical primer design considerations, the design of primers for high-resolution melting assays involves maximizing the thermodynamic differences between PCR products belonging to different genotypes. Smaller amplicons generally yield greater melting temperature variation than longer amplicons, but the variability cannot be ...

  8. GC-content - Wikipedia

    en.wikipedia.org/wiki/GC-content

    A higher GC-content level indicates a relatively higher melting temperature. Many sequencing technologies, such as Illumina sequencing , have trouble reading high-GC-content sequences. Bird genomes are known to have many such parts, causing the problem of "missing genes" expected to be present from evolution and phenotype but never sequenced ...

  9. Primer (molecular biology) - Wikipedia

    en.wikipedia.org/wiki/Primer_(molecular_biology)

    Pairs of primers should have similar melting temperatures since annealing during PCR occurs for both strands simultaneously, and this shared melting temperature must not be either too much higher or lower than the reaction's annealing temperature. A primer with a T m (melting temperature) too much higher than the reaction's annealing ...