<p>The <i>Cy0</i> and <i>Cy0<sub>corrected</sub></i> values were calculated from the independent freely available data set named “Competimer”, reported in Ruijter et al. <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0068481#pone.0068481-Ruijter1" target="_blank">[32]</a>. Briefly, the amplification curves were obtained using decreasing input gDNA amounts (64, 16, 4, 1, 0.25 and 0.0625 ng/µl) and in optimal (% Competimer = 0–5) and inhibited (increasing % Competimer from 10 to 50%) amplification conditions. The and parameters were estimated from optimal amplification conditions. Panel (A) shows <i>Cy0</i> and <i>Cy0<sub>corrected</sub></i> values obtained for each condition; Panel (B) shows the standard deviation ca...
<p>Number of molecules per microliter (mol/µl) of the target DNA in the extracts are listed for each...
In the analysis of quantitative PCR (qPCR) data, the quantification cycle (Cq) indicates the positio...
AbstractWe have examined the imprecision in the estimation of PCR efficiency by means of standard cu...
Quantitative real-time PCR represents a highly sensitive and powerful technology for the quantificat...
<div><p>Quantitative real-time PCR represents a highly sensitive and powerful technology for the qua...
Quantitative real-time PCR represents a highly sensitive and powerful technology for the quantificat...
Background: Real-time PCR analysis is a sensitive DNA quantification technique that has recently gai...
<p>Panel (A) shows amplification plots obtained for each condition; (B) shows the relative errors <i...
Quantitative real-time RT-PCR is the most sensitive and widely used method for the measurement of ge...
"nFluorescent monitoring of DNA amplification is the basis of real-time PCR. Absolute quantific...
<p><b>Copyright information:</b></p><p>Taken from "Standardisation of data from real-time quantitati...
Quantification of residual disease by real-time polymerase chain reaction (PCR) will become a pivota...
textabstractQuantification of residual disease by real-time polymerase chain reaction (PCR) wi...
Genomic DNA (gDNA) contamination is an inherent problem during RNA purification that can lead to non...
Current methodology in real-time Polymerase chain reaction (PCR) analysis performs well provided PCR...
<p>Number of molecules per microliter (mol/µl) of the target DNA in the extracts are listed for each...
In the analysis of quantitative PCR (qPCR) data, the quantification cycle (Cq) indicates the positio...
AbstractWe have examined the imprecision in the estimation of PCR efficiency by means of standard cu...
Quantitative real-time PCR represents a highly sensitive and powerful technology for the quantificat...
<div><p>Quantitative real-time PCR represents a highly sensitive and powerful technology for the qua...
Quantitative real-time PCR represents a highly sensitive and powerful technology for the quantificat...
Background: Real-time PCR analysis is a sensitive DNA quantification technique that has recently gai...
<p>Panel (A) shows amplification plots obtained for each condition; (B) shows the relative errors <i...
Quantitative real-time RT-PCR is the most sensitive and widely used method for the measurement of ge...
"nFluorescent monitoring of DNA amplification is the basis of real-time PCR. Absolute quantific...
<p><b>Copyright information:</b></p><p>Taken from "Standardisation of data from real-time quantitati...
Quantification of residual disease by real-time polymerase chain reaction (PCR) will become a pivota...
textabstractQuantification of residual disease by real-time polymerase chain reaction (PCR) wi...
Genomic DNA (gDNA) contamination is an inherent problem during RNA purification that can lead to non...
Current methodology in real-time Polymerase chain reaction (PCR) analysis performs well provided PCR...
<p>Number of molecules per microliter (mol/µl) of the target DNA in the extracts are listed for each...
In the analysis of quantitative PCR (qPCR) data, the quantification cycle (Cq) indicates the positio...
AbstractWe have examined the imprecision in the estimation of PCR efficiency by means of standard cu...