estimateSI {nbTransmission} | R Documentation |
Estimates the generation/serial interval distribution
Description
The function estimateSI
uses the relative transmission probabilities to estimate
the generation/serial interval distribution assuming a gamma distribution.
It uses the PEM algorithm developed by Hens et al. 2012 extending their method to include
restricting analysis to the top cluster of possible infectors.
Usage
estimateSI(
df,
indIDVar,
timeDiffVar,
pVar,
clustMethod = c("none", "n", "kd", "hc_absolute", "hc_relative"),
cutoffs = NULL,
initialPars,
shift = 0,
epsilon = 1e-05,
bootSamples = 0,
alpha = 0.05,
progressBar = TRUE
)
Arguments
df |
The name of the dateset with transmission probabilities (column |
indIDVar |
The name (in quotes) of the individual ID columns
(data frame |
timeDiffVar |
The name (in quotes) of the column with the difference in time between infection (generation interval) or symptom onset (serial interval) for the pair of cases. The units of this variable (hours, days, years) defines the units of the resulting distribution. |
pVar |
The column name (in quotes) of the transmission probabilities. |
clustMethod |
The method used to cluster the infectors; one of
|
cutoffs |
A vector of cutoffs for clustering (see |
initialPars |
A vector of length two with the shape and scale to initialize the gamma distribution parameters. |
shift |
A value in the same units as |
epsilon |
The difference between successive estimates of the shape and scale parameters that indicates convergence. |
bootSamples |
The number of bootstrap samples; if 0, then no confidence intervals are calculated. |
alpha |
The alpha level for the confidence intervals. |
progressBar |
A logical indicating if a progress bar should be printed (default is TRUE). |
Details
The PEM algorithm uses the prior probability that each pair is connected by direct
transmission to estimate the generation/serial interval using estimation maximization.
This code will provide an estimate of the generation interval if timeDiffVar
represents the
difference in infection dates and the serial interval if it represents the difference in symptom onset dates.
The current generation/serial interval distribution parameters are used to update the probabilities
which are then used to update the generation/serial interval distribution parameters. The process
continues until the parameters converge (indicated by a change of less than epsilon
)
between iterations. Note: time difference between pairs should not be used to
estimate the probabilities
This function acts as a wrapper around performPEM
which integrates
estimation of the generation/serial interval distribution with clustering the infectors and calculates
derived parameters (mean, median, sd) of the distribution. Generally, this function
should be called instead of performPEM
directly.
All pairs of cases can be used in the estimation process by setting
clustMethod = "none"
. However, if the probabilities are from a algorithm such as
nbProbabilities
, then it is recommeneded to use a clustering method
and only include the top cluster of infectors for infectees which have such a cluster.
This can be specified by using the clustMethod
and cutoff
arguments which
are passed into clusterInfectors
. See the details of this function for
a description of the different clustering methods.
The method can be performed with any generation/serial interval distribution,
but this version of this function assumes that the generation/serial interval has a gamma distribution.
The function does allow for a shifted gamma distribution. The shift
argument
defines how much the gamma distribution should be shifted. Any observed generation/serial intervals
that are less than this shift will have probability 0. This parameter should be used if
there is a clinical lower bound for the possible generation/serial interval. If this argument
is not specified then an unmodified gamma function is used. The units of the
estimated gamma distribution will be defined by the units of the provided
<timeDiffVar>
column. The value of the shift
should be in the same units.
The algorithm requires initial parameters which should be specified as a vector:
c(<shape>, <scale>)
. These parameters should result in a gamma distribution
that is on the desired scale, set by the <timeDiffVar>
column.
If bootSamples > 0
, bootstrap confidence intervals will be estimated for
both the shape and scale parameters as well as the mean, median, and mode of the
distribution using cluster bootstrapping.
Value
A data frame with one row and the following columns:
-
nIndividuals
- the number of infectees who have intervals included in the estimate. -
pCluster
- the proportion of cases who have intervals included in the estimate. -
nInfectors
- the average number of infectors in the top cluster. -
shape
- the shape of the estimated gamma distribution for the interval -
scale
- the scale of the estimated gamma distribution for the interval -
meanSI
- the mean of the estimated gamma distribution for the interval (shape * scale + shift
) -
medianSI
- the median of the estimated gamma distribution for the interval (qgamma(0.5, shape, scale) + shift)
) -
sdSI
- the standard deviation of the estimated gamma distribution for the interval (shape * scale ^ 2
)
If bootSamples > 0, then the data frame also includes the following columns:
-
shapeCILB
andshapeCIUB
- lower bound and upper bounds of the bootstrap confidence interval for the shape parameter -
scaleCILB
andscaleCIUB
- lower bound and upper bounds of the bootstrap confidence interval for the scale parameter -
meanCILB
andmeanCIUB
- lower bound and upper bounds of the bootstrap confidence interval for the mean of the interval distribution -
medianCILB
andmedianCIUB
- lower bound and upper bounds of the bootstrap confidence interval for the median of the interval distribution -
sdCILB
andsdCIUB
- lower bound and upper bounds of the bootstrap confidence interval for the sd of the interval distribution
References
Hens N, Calatayud L, Kurkela S, Tamme T, Wallinga J. Robust reconstruction and analysis of outbreak data: influenza A (H1N1) v transmission in a school-based population. American Journal of Epidemiology. 2012 Jul 12;176(3):196-203.
See Also
nbProbabilities
clusterInfectors
performPEM
Examples
## First, run the algorithm without including time as a covariate.
orderedPair <- pairData[pairData$infectionDiffY > 0, ]
## Create a variable called snpClose that will define probable links
# (<3 SNPs) and nonlinks (>12 SNPs) all pairs with between 2-12 SNPs
# will not be used to train.
orderedPair$snpClose <- ifelse(orderedPair$snpDist < 3, TRUE,
ifelse(orderedPair$snpDist > 12, FALSE, NA))
table(orderedPair$snpClose)
## Running the algorithm
# NOTE should run with nReps > 1.
resGen <- nbProbabilities(orderedPair = orderedPair,
indIDVar = "individualID",
pairIDVar = "pairID",
goldStdVar = "snpClose",
covariates = c("Z1", "Z2", "Z3", "Z4"),
label = "SNPs", l = 1,
n = 10, m = 1, nReps = 1)
## Merging the probabilities back with the pair-level data
nbResultsNoT <- merge(resGen[[1]], orderedPair, by = "pairID", all = TRUE)
## Estimating the serial interval
# Using hierarchical clustering with a 0.05 absolute difference cutoff
estimateSI(nbResultsNoT, indIDVar = "individualID",
timeDiffVar = "infectionDiffY", pVar = "pScaled",
clustMethod = "hc_absolute", cutoff = 0.05, initialPars = c(2, 2))
# Using all pairs
estimateSI(nbResultsNoT, indIDVar = "individualID",
timeDiffVar = "infectionDiffY", pVar = "pScaled",
clustMethod = "none", initialPars = c(2, 2))
# # Using a shifted gamma distribution:
# # not allowing serial intervals of less than 3 months (0.25 years)
estimateSI(nbResultsNoT, indIDVar = "individualID",
timeDiffVar = "infectionDiffY", pVar = "pScaled",
clustMethod = "hc_absolute", cutoff = 0.05,
initialPars = c(2, 2), shift = 0.25)
# # Using multiple cutoffs
estimateSI(nbResultsNoT, indIDVar = "individualID",
timeDiffVar = "infectionDiffY", pVar = "pScaled",
clustMethod = "hc_absolute", cutoff = c(0.025, 0.05), initialPars = c(2, 2))
## Adding confidence intervals
# NOTE should run with bootSamples > 2.
estimateSI(nbResultsNoT, indIDVar = "individualID",
timeDiffVar = "infectionDiffY", pVar = "pScaled",
clustMethod = "hc_absolute", cutoff = 0.05,
initialPars = c(2, 2), shift = 0.25, bootSamples = 2)