a<p>A<sub>n</sub> = A<sub>0</sub> = A = initial copy number of DNA template (Ci).</p>b<p>B<sub>n</sub> = A×E+B<sub>n−1</sub>×1 (B<sub>0</sub> = 0).</p>c<p>C<sub>n</sub> = B<sub>n−1</sub>×1+C<sub>n−1</sub>×2 (C<sub>0</sub> = C<sub>1</sub> = 0).</p>d<p>D<sub>n</sub> = A<sub>n</sub>+B<sub>n</sub>+C<sub>n</sub>.</p>e<p>Bias = (compromised yield−theoretical yield)/theoretical yield×100%.</p
a<p>The fidelity of DNA replication during PCR supplied with UDG and/or EndoIV was measured using a ...
<p>Effect of sample preparation method on PCR success (%), measured as the number of positive amplic...
The developments of the polymerase chain reaction (PCR) and the short tandem repeat multiplex kits i...
<p>E<sub>i</sub> (initial PCR efficiency): the efficiency of type I amplification. E<sub>ii</sub>: t...
The polymerase chain reaction (PCR) has found wide application in biochemistry and molecular biology...
<div><p>Accurate estimation of template - DNA or RNA by real time PCR is dependent on the amplificat...
The success of PCR is partly based on its exponential amplifica-tion characteristics. Nevertheless, ...
Accurate estimation of template--DNA or RNA by real time PCR is dependent on the amplification effic...
Recently a theoretical analysis of PCR efficiency has been published by Booth et al., (2010). The PC...
<p>PCR efficiency (%) obtained from slope of dependence of DNA concentrations on threshold cycle (Ct...
The rate of amplification of abundant PCR products generally declines faster than that of less abund...
Competitive PCR is a highly sensitive method for specific DNA quantification. Despite the lack of st...
Polymerase stop assays used to quantify DNA damage assume that single lesions are sufficient to bloc...
<p>(A) Second round amplification result (C<sub>T</sub> value of <i>ETH225</i>). Six sample amount g...
a<p><i>y</i> = C<sub>t</sub> value (PCR cycle value at the fluorescence threshold of 0.1 for PC gene...
a<p>The fidelity of DNA replication during PCR supplied with UDG and/or EndoIV was measured using a ...
<p>Effect of sample preparation method on PCR success (%), measured as the number of positive amplic...
The developments of the polymerase chain reaction (PCR) and the short tandem repeat multiplex kits i...
<p>E<sub>i</sub> (initial PCR efficiency): the efficiency of type I amplification. E<sub>ii</sub>: t...
The polymerase chain reaction (PCR) has found wide application in biochemistry and molecular biology...
<div><p>Accurate estimation of template - DNA or RNA by real time PCR is dependent on the amplificat...
The success of PCR is partly based on its exponential amplifica-tion characteristics. Nevertheless, ...
Accurate estimation of template--DNA or RNA by real time PCR is dependent on the amplification effic...
Recently a theoretical analysis of PCR efficiency has been published by Booth et al., (2010). The PC...
<p>PCR efficiency (%) obtained from slope of dependence of DNA concentrations on threshold cycle (Ct...
The rate of amplification of abundant PCR products generally declines faster than that of less abund...
Competitive PCR is a highly sensitive method for specific DNA quantification. Despite the lack of st...
Polymerase stop assays used to quantify DNA damage assume that single lesions are sufficient to bloc...
<p>(A) Second round amplification result (C<sub>T</sub> value of <i>ETH225</i>). Six sample amount g...
a<p><i>y</i> = C<sub>t</sub> value (PCR cycle value at the fluorescence threshold of 0.1 for PC gene...
a<p>The fidelity of DNA replication during PCR supplied with UDG and/or EndoIV was measured using a ...
<p>Effect of sample preparation method on PCR success (%), measured as the number of positive amplic...
The developments of the polymerase chain reaction (PCR) and the short tandem repeat multiplex kits i...