Description Usage Arguments Details Value Author(s) References Examples
The LRE method is based on a linear regression of raw fluorescence versus efficiency, with the final aim to obtain cycle dependent individual efficiencies E_n. A linear model is then fit to a sliding window of defined size(s) and within a defined border. Regression coefficients are calculated for each window, and from the window of maximum regression, parameters such as PCR efficiency and initial template fluorescence are calculated. See 'Details' for more information. This approach is quite similar to the one in sliwin
, but while sliwin
regresses cycle number versus log(fluorescence), LRE
regresses raw fluorescence versus efficiency. Hence, the former is based on assuming a constant efficiency for all cycles while the latter is based on a per-cycle individual efficiency.
1 2 |
object |
an object of class 'pcrfit'. |
wsize |
the size(s) of the sliding window(s), default is |
basecyc |
if |
base |
either |
border |
either |
plot |
if |
verbose |
logical. If |
... |
only used internally for passing the parameter matrix. |
To avoid fits with a high R^2 in the baseline region, some border in the data must be defined. In LRE
, this is by default (base = NULL
) the region in the curve starting at the take-off cycle (top) as calculated from takeoff
and ending at the transition region to the upper asymptote (saturation region). The latter is calculated from the first and second derivative maxima: asympt = cpD1 + (cpD1 - cpD2). If the border is to be set by the user, border
values such as c(-2, 4)
extend these values by top + border[1] and asympt + border[2]. The efficiency is calculated by E_n = \frac{F_n}{F_{n-1}} and regressed against the raw fluorescence values F: E = Fβ + ε. For the baseline optimization, 100 baseline values Fb_i are interpolated in the range of the data:
F_{min} ≤ Fb_i ≤ base \cdot σ(F_{basecyc[1]}...F_{basecyc[2]})
and subtracted from F_n. For all iterations, the best regression window in terms of R^2 is found and its parameters returned.
Two different initial template fluorescence values F_0 are calculated in LRE
:
init1
: Using the single maximum efficiency E_{max} (the intercept of the best fit) and the fluorescence at second derivative maximum F_{cpD2}, by
F_0 = \frac{F_{cpD2}}{E_{max}^{cpD2}}
init2
: Using the cycle dependent efficiencies E_n from n = 1 to the near-lowest integer (floor) cycle of the second derivative maximum n = \lfloor cpD2 \rfloor, and the fluorescence at the floor of the second derivative maximum F_{\lfloor cpD2 \rfloor}, by
F_0 = \frac{F_{\lfloor cpD2 \rfloor}}{∏ E_n}
This approach corresponds to the paradigm described in Rutledge & Stewart (2008), by using cycle-dependent and decreasing efficiencies Δ_E to calculate F_0.
A list with the following components:
eff |
the maximum PCR efficiency E_{max} calculated from the best window. |
rsq |
the maximum R^2. |
base |
the optimized baseline value. |
window |
the best window found within the |
parMat |
a matrix containing the parameters as above for each iteration. |
init1 |
the initial template fluorescence F_0 assuming constant efficiency E_{max} as described under 'Details'. |
init2 |
the initial template fluorescence F_0, assuming cycle-dependent efficiency E_n as described under 'Details'. |
Andrej-Nikolai Spiess
A kinetic-based sigmoidal model for the polymerase chain reaction and its application to high-capacity absolute quantitative real-time PCR.
Rutledge RG & Stewart D.
BMC Biotech (2008), 8: 47.
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