flFitLinear {QurvE} | R Documentation |
Data fit via a heuristic linear method
Description
Determine maximum slopes from using a heuristic approach similar to the “growth rates made easy”-method of Hall et al. (2013).
Usage
flFitLinear(
time = NULL,
growth = NULL,
fl_data,
ID = "undefined",
quota = 0.95,
control = fl.control(x_type = c("growth", "time"), log.x.lin = FALSE, log.y.lin =
FALSE, t0 = 0, min.growth = NA, lin.h = NULL, lin.R2 = 0.98, lin.RSD = 0.05, lin.dY =
0.05, biphasic = FALSE)
)
Arguments
time |
Vector of the independent time variable (if x_type = "time" in control object). |
growth |
Vector of the independent time growth (if x_type = "growth" in control object). |
fl_data |
Vector of the dependent fluorescence variable. |
ID |
(Character) The name of the analyzed sample. |
quota |
(Numeric, between 0 an 1) Define what fraction of |
control |
A |
Value
A gcFitLinear
object with parameters of the fit. The lag time is
estimated as the intersection between the fit and the horizontal line with
y=y_0
, where y0
is the first value of the dependent variable.
Use plot.gcFitSpline
to visualize the linear fit.
raw.x |
Filtered x values used for the spline fit. |
raw.fl |
Filtered fluorescence values used for the spline fit. |
filt.x |
Filtered x values. |
filt.fl |
Filtered fluorescence values. |
ID |
(Character) Identifies the tested sample. |
FUN |
Linear function used for plotting the tangent at mumax. |
fit |
|
par |
List of determined fluorescence parameters: |
-
y0
: Minimum fluorescence value considered for the heuristic linear method. -
dY
: Difference in maximum fluorescence and minimum fluorescence -
A
: Maximum fluorescence -
y0_lm
: Intersection of the linear fit with the abscissa. -
max_slope
: Maximum slope of the linear fit. -
tD
: Doubling time. -
slope.se
: Standard error of the maximum slope. -
lag
: Lag X. -
x.max_start
: X value of the first data point within the window used for the linear regression. -
x.max_end
: X value of the last data point within the window used for the linear regression. -
x.turn
: For biphasic: X at the inflection point that separates two phases. -
max.slope2
: For biphasic: Slope of the second phase. -
tD2
: Doubling time of the second phase. -
y0_lm2
: For biphasic: Intersection of the linear fit of the second phase with the abscissa. -
lag2
: For biphasic: Lag time determined for the second phase.. -
x.max2_start
: For biphasic: X value of the first data point within the window used for the linear regression of the second phase. -
x.max2_end
: For biphasic: X value of the last data point within the window used for the linear regression of the second phase.
ndx |
Index of data points used for the linear regression. |
ndx2 |
Index of data points used for the linear regression for the second phase. |
control |
Object of class |
rsquared |
R2 of the linear regression. |
rsquared2 |
R2 of the linear regression for the second phase. |
fitFlag |
(Logical) Indicates whether linear regression was successfully performed on the data. |
fitFlag2 |
(Logical) Indicates whether a second phase was identified. |
reliable |
(Logical) Indicates whether the performed fit is reliable (to be set manually). |
References
Hall, BG., Acar, H, Nandipati, A and Barlow, M (2014) Growth Rates Made Easy. Mol. Biol. Evol. 31: 232-38, DOI: 10.1093/molbev/mst187
Petzoldt T (2022). growthrates: Estimate Growth Rates from Experimental Data. R package version 0.8.3, https://CRAN.R-project.org/package=growthrates.
Examples
# load example dataset
input <- read_data(data.growth = system.file("lac_promoters_growth.txt", package = "QurvE"),
data.fl = system.file("lac_promoters_fluorescence.txt", package = "QurvE"),
csvsep = "\t",
csvsep.fl = "\t")
# Extract time and normalized fluorescence data for single sample
time <- input$time[4,]
data <- input$norm.fluorescence[4,-(1:3)] # Remove identifier columns
# Perform linear fit
TestFit <- flFitLinear(time = time,
fl_data = data,
ID = "TestFit",
control = fl.control(fit.opt = "l", x_type = "time",
lin.R2 = 0.95, lin.RSD = 0.1,
lin.h = 20))
plot(TestFit)