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Multivariate operations

Work in progress! 🏗

Element-wise operations

Most operations in this model are element-wise, meaning each calculation occurs independently on matching elements across nodes. These operations preserve node dimensions while applying functions (such as multiplication or addition) to corresponding elements, allowing uncertainties and variates to propagate through the calculations.

Row matching

Row matching operations align nodes to ensure they have compatible dimensions and properly matched rows for element-wise calculations. This is especially important when working with nodes containing different scenarios. The matching process may require reordering, duplicating, or adding rows to either or both nodes.

Row matching between nodes is needed in the following cases and their combinations:

Group matching

Nodes with same scenarios/dimensions but different group order

  1. Check if keys that define groups are in a different order

  1. Assign common group ids, based on keys

  1. Reorder rows to align group ids. This is similar to dplyr left_join

Scenario matching

Nodes with same groups but different scenarios. The general rule for these operations is that when no scenario is specified, it is assumed that a variable takes the values from the baseline scenario.

  1. Check if scenarios are different

  1. For missing scenarios, duplicate the baseline scenario (scenario “0”)

  1. When nodes matched by scenario are used in an element-wise operation, the resulting node will contain all scenarios from both input nodes. This is conceptually similar to a dplyr full_join, except that any unmatched rows use values from the baseline scenario.

Null matching

When nodes contain different scenarios and groups, some groups may be missing from certain nodes. These missing groups (called “null” variates) are assigned a probability of 0. This operation typically complements scenario matching.

  1. Check for missing groups

  1. Add null variates with probability 0 for any missing groups (and apply scenario matching)

  1. When nodes are matched by scenario in an element-wise operation, the resulting node will contain all groups from both input nodes

Combined probabilities

A special type of element-wise operation that automatically deals with row matching. Combines probabilities of multiple events assuming independence, using the formula:

\[ P(A \cup B) = 1 - (1-P(A))(1-P(B))\]

Row aggregation

Row aggregation operations combine values across multiple rows (variates) in an mcnode using specific criteria. These operations calculate overall probabilities or sum quantities across groups.

Probabilities

Some events can occur independently across multiple variates of the same node. For example, a disease might be present in animals from different regions or farms. To calculate the probability of an event occurring in at least one variate within a subset, we first group the data by aggregation keys (agg_keys). Then, for each subset, we use the standard probability formula for independent trials to find the probability of the event occurring in at least one variate.

\[ p\_{agg}=1-\prod_{p\subseteq S}(1-p) \]

Where:

Row aggregation by pathogen. The calculation is performed element-wise across subset variates to maintain uncertainty propagation.
Row aggregation by pathogen. The calculation is performed element-wise across subset variates to maintain uncertainty propagation.

If scenarios are being simulated, scenario id must always be included as an aggregation key, as probabilities are not calculated across different what-if scenarios.

You can also keep all variariates, with their corresponding aggregated values, to ensure dimensions compatibility in further calculations.

Default row aggregation and row aggregation keeping all variates
Default row aggregation and row aggregation keeping all variates

Quantities

When working with quantities (such as number of animals or farms), we calculate totals by summing values across variates within each subset.

\[ n\_{agg}=\sum_{n\subseteq S} n \]

Where:

Trials

In this framework, nodes typically represent the probability of success for a single trial with a binary outcome (success/failure). A trial is one instance where an event might occur, for example, an animal, farm, batch, animal movement, or farm visit. Each trial has two possible outcomes, such as whether an animal is infected or not, or whether a test is positive or negative. In single-level trials, all trials are independent and have the same probability of success1.

Some probability processes follow a hierarchical structure where events occur at different levels. For example, when animals are purchased from multiple farms, we must consider both the probability of a farm being infected and the probability of an individual animal within that farm being infected. This means infection probabilities for animals from the same farm are not independent. In multilevel trials, trials are organized into subsets, with each subset having its own selection probability. A subset represents a group sharing specific characteristics, for example, animals from the same farm or with the same health status.

Most of the following probability processes and calculations are based on Chapter 5 of the Handbook on Import Risk Analysis for Animals and Animal Products Volume 2. Quantitative risk assessment (Murray 2004).

Single-level trials

In single-level trials, each trial is independent with the same probability of success (\(trial\_p\)). For a set of \(trials\_n\) trials, the probability of at least one success is:

\[ set\_p= 1-(1-trial\_p)^{trials\_n} \]

In imports_mcmodule, we have the probability that an infected animal from an infected farm goes undetected (\(no\_detect\_a\)). When all animals (in a variate) have the same probability, we can use the total number of animals selected per farm (\(animals\_n\)) as the number of trials (trials_n) to determine the probability that at least one infected animal from one farm is not detected (\(no\_detect\_set\)). Note that while \(animals\_n\) isn’t defined as an mcnode in imports_mcmodule (not used in imports_mcmodule$model_exp), it can be automatically generated in trial_totals() because it’s included in imports_mctable and the required data exists in imports_mcmodule$data.

# Single-level trial
imports_mcmodule <- trial_totals(
  mcmodule = imports_mcmodule,
  mc_names = "no_detect_a", # trial_p
  trials_n = "animals_n",
  mctable = imports_mctable
)

# Probability that at least one infected animal from an infected farm is not detected
mc_summary(imports_mcmodule,"no_detect_a_set")[,-1]
#>   pathogen origin      mean           sd       Min      2.5%       25%
#> 1        a   nord 0.9999351 6.729257e-05 0.9995022 0.9997581 0.9999101
#> 2        a  south 0.9999947 9.153405e-06 0.9998899 0.9999707 0.9999940
#> 3        a   east 1.0000000 8.787173e-10 1.0000000 1.0000000 1.0000000
#> 4        b   nord 0.9994302 8.088769e-04 0.9935978 0.9971028 0.9993713
#> 5        b  south 1.0000000 5.171354e-14 1.0000000 1.0000000 1.0000000
#> 6        b   east 1.0000000 0.000000e+00 1.0000000 1.0000000 1.0000000
#>         50%       75%     97.5%       Max  nsv Na's
#> 1 0.9999564 0.9999830 0.9999949 0.9999986 1001    0
#> 2 0.9999980 0.9999993 0.9999999 1.0000000 1001    0
#> 3 1.0000000 1.0000000 1.0000000 1.0000000 1001    0
#> 4 0.9997308 0.9998989 0.9999803 0.9999946 1001    0
#> 5 1.0000000 1.0000000 1.0000000 1.0000000 1001    0
#> 6 1.0000000 1.0000000 1.0000000 1.0000000 1001    0

Multilevel trials

Simple multilevel

In multilevel trials, we account for hierarchical structures where trials are organized into subsets. For example, when considering animals (\(trials\_n\)) from different farms (\(subset\_n\)), we must account for both the farm’s selection probability (\(subset\_p\)) and the individual animal’s probability of success (\(trial\_p\)).

The probability of at least one success in this hierarchical structure is given by:

\[ set\_p= 1-(1-subset\_p \cdot (1-(1-trial\_p)^{trial\_n}))^{subset\_n} \]

Where:

When considering animals (trials_n) from different farms (subset_n, we must account for both the farm’s probability of being infected (subsets_p) and the individual animal’s probability of being infected (trial_p).

# Simple multilevel trial
imports_mcmodule <- trial_totals(
  mcmodule = imports_mcmodule,
  mc_names = "no_detect_a", # trial_p
  trials_n = "animals_n",
  subsets_n = "farms_n",
  subsets_p = "h_prev",
  mctable = imports_mctable
)

# Probability that at least one infected animal from at least one farm is not detected
mc_summary(imports_mcmodule,"no_detect_a_set", digits=2)[,-1]
#>   pathogen origin mean     sd  Min 2.5%  25%  50%  75% 97.5%  Max  nsv Na's
#> 1        a   nord 0.38 0.0200 0.34 0.34 0.36 0.38 0.39  0.41 0.41 1001    0
#> 2        a  south 0.30 0.0600 0.18 0.19 0.24 0.30 0.35  0.40 0.40 1001    0
#> 3        a   east 0.61 0.0500 0.52 0.53 0.57 0.61 0.65  0.68 0.68 1001    0
#> 4        b   nord 0.99 0.0082 0.97 0.97 0.98 0.99 0.99  1.00 1.00 1001    0
#> 5        b  south 0.96 0.0080 0.94 0.94 0.95 0.96 0.97  0.97 0.97 1001    0
#> 6        b   east 0.97 0.0200 0.92 0.92 0.95 0.97 0.98  0.99 0.99 1001    0

Multiple group multilevel trials

In multiple group multilevel trials, several variates (groups) can belong to the same subset. For example, when selecting animals of different categories (cow, calf, heifer, bull) from the same farm, their infection probabilities are not independent. You should include aggregation keys for groups that are not independent to calculate their trial probabilities, for example, aggregating variates for different animal categories by farm. For this calculation, the subset_p and subset_n values must be identical across all variates being aggregated.

\[ trial\_p\_agg=1-\prod_{trial\_p\subseteq S}(1-trial\_p)^{trial\_n} \]

\[ set\_p\_agg = 1-(1-subset\_p \cdot trial\_p\_agg)^{subset\_n} \]

Where:

As with row aggregation, you can keep all variates to maintain dimensions compatibility in further calculations.

Murray, Noel. 2004. Handbook on Import Risk Analysis for Animals and Animal Products Volume 2 Quantitative Risk Assessment. Vol. 2. https://rr-africa.woah.org/app/uploads/2018/03/handbook_on_import_risk_analysis_-_oie_-_vol_ii.pdf.

  1. In this context, a “success” refers to the occurrence of an event of interest, which may actually represent an undesirable outcome such as the presence of a disease or a positive test result for a pathogen.↩︎

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