View source: R/metrics-sample.R
pit_histogram_sample | R Documentation |
Uses a Probability integral transformation (PIT) (or a randomised PIT for integer forecasts) to assess the calibration of predictive Monte Carlo samples.
pit_histogram_sample(
observed,
predicted,
quantiles,
integers = c("nonrandom", "random", "ignore"),
n_replicates = NULL
)
observed |
A vector with observed values of size n |
predicted |
nxN matrix of predictive samples, n (number of rows) being
the number of data points and N (number of columns) the number of Monte
Carlo samples. Alternatively, |
quantiles |
A vector of quantiles between which to calculate the PIT. |
integers |
How to handle integer forecasts (count data). This is based on methods described Czado et al. (2007). If "nonrandom" (default) the function will use the non-randomised PIT method. If "random", will use the randomised PIT method. If "ignore", will treat integer forecasts as if they were continuous. |
n_replicates |
The number of draws for the randomised PIT for discrete
predictions. Will be ignored if forecasts are continuous or |
Calibration or reliability of forecasts is the ability of a model to correctly identify its own uncertainty in making predictions. In a model with perfect calibration, the observed data at each time point look as if they came from the predictive probability distribution at that time.
Equivalently, one can inspect the probability integral transform of the predictive distribution at time t,
u_t = F_t (x_t)
where x_t
is the observed data point at time t \textrm{ in } t_1,
…, t_n
, n being the number of forecasts, and F_t
is
the (continuous) predictive cumulative probability distribution at time t. If
the true probability distribution of outcomes at time t is G_t
then the
forecasts F_t
are said to be ideal if F_t = G_t
at all times t.
In that case, the probabilities u_t
are distributed uniformly.
In the case of discrete nonnegative outcomes such as incidence counts, the PIT is no longer uniform even when forecasts are ideal. In that case two methods are available ase described by Czado et al. (2007).
By default, a nonrandomised PIT is calculated using the conditional cumulative distribution function
F(u) =
\begin{cases}
0 & \text{if } v < P_t(k_t - 1) \\
(v - P_t(k_t - 1)) / (P_t(k_t) - P_t(k_t - 1)) & \text{if } P_t(k_t - 1) \leq v < P_t(k_t) \\
1 & \text{if } v \geq P_t(k_t)
\end{cases}
where k_t
is the observed count, P_t(x)
is the predictive
cumulative probability of observing incidence k
at time t
and
P_t (-1) = 0
by definition.
Values of the PIT histogram are then created by averaging over the n
predictions,
\bar{F}(u) = \frac{i = 1}{n} \sum_{i=1}^{n} F^{(i)}(u)
And calculating the value at each bin between quantile q_i
and quantile
q_{i + 1}
as
\bar{F}(q_i) - \bar{F}(q_{i + 1})
Alternatively, a randomised PIT can be used instead. In this case, the PIT is
u_t = P_t(k_t) + v * (P_t(k_t) - P_t(k_t - 1))
where v
is standard uniform and independent of k
. The values of
the PIT histogram are then calculated by binning the u_t
values as above.
A vector with PIT histogram densities for the bins corresponding to the given quantiles.
Claudia Czado, Tilmann Gneiting Leonhard Held (2009) Predictive model assessment for count data. Biometrika, 96(4), 633-648. Sebastian Funk, Anton Camacho, Adam J. Kucharski, Rachel Lowe, Rosalind M. Eggo, W. John Edmunds (2019) Assessing the performance of real-time epidemic forecasts: A case study of Ebola in the Western Area region of Sierra Leone, 2014-15, \Sexpr[results=rd]{tools:::Rd_expr_doi("10.1371/journal.pcbi.1006785")}
get_pit_histogram()
## continuous predictions
observed <- rnorm(20, mean = 1:20)
predicted <- replicate(100, rnorm(n = 20, mean = 1:20))
pit <- pit_histogram_sample(observed, predicted, quantiles = seq(0, 1, 0.1))
## integer predictions
observed <- rpois(20, lambda = 1:20)
predicted <- replicate(100, rpois(n = 20, lambda = 1:20))
pit <- pit_histogram_sample(observed, predicted, quantiles = seq(0, 1, 0.1))
## integer predictions, randomised PIT
observed <- rpois(20, lambda = 1:20)
predicted <- replicate(100, rpois(n = 20, lambda = 1:20))
pit <- pit_histogram_sample(
observed, predicted, quantiles = seq(0, 1, 0.1),
integers = "random", n_replicates = 30
)
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