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Monitoring
Part of the simulation design process is also deciding which results of the simulation should be captured with a monitoring statement. Not all the data produced by the simulation is needed to interpret the results: mosquito-to-human transmission intensity, parasite density per infection per human together with human infectiousness to mosquitoes, bouts of sickness and treatments affecting each human, etc. A summary of those events over all the simulated population may be more important than the detailed experience of each simulated individual.
The monitoring method is described by an XML element of the form below. The continuous
element is optional and describes continuous reporting, while the other three elements are required and describe surveys.
<monitoring name="(some description or name)">
<continuous ... />
<SurveyOptions ... />
<surveys ... />
<ageGroup ... />
</monitoring>
Standard outputs from OpenMalaria are intended to simulate the collection of data at a cross-sectional survey of the whole population. The measures output may include cross-sectional data from the time of the survey and/or values summed over the population since the previous survey. Exactly which measures will be output by a simulation depends on the SurveyOptions
element. This contains a list of options, for example:
<SurveyOptions>
<option name="nHost" value="true"/>
<option name="nPatent" value="true"/>
<option name="nMassVaccinations"/>
</SurveyOptions>
(The value
attribute is optional and can be omitted as in the last example. It can also be explicitly set to "false" which is the same as omitting the option entirely.)
A list of all outputs currently implemented can be found here.
Surveys can take place at any time point, starting from the beginning of the intervention period. Surveys only report events which happened from the beginning of the time-step of the last survey until the end of the time-step before the current survey time-step, and measures of the current state (such as the number of patent hosts) from the beginning of the survey time-step.
The timing of these is described as in the XML fragment below. The first valid time-point for a survey is time-step 0; however, any events happening before time-step 0 are not reported, so measures of events (such as infectious bites received) will be zero.
<surveys detectionLimit="40">
<surveyTime>18</surveyTime>
<surveyTime>37</surveyTime>
<surveyTime>55</surveyTime>
<surveyTime>73</surveyTime>
</surveys>
This example describes four quarterly surveys (assuming a 5-day time-step); these are reported in the output.txt file as surveys 1, 2, 3 and 4. (The detectionLimit
attribute describes the minimum parasite density (parasites per µl/microlitre) at which a human is counted as having a patent infection.)
Timestep 0 will always correspond to the first of January (up to 5th Jan with a 5-day timestep), except that, prior to schema 22, when the maximumAgeYrs attribute of demography was not a whole number of years timestep values may well have been offset. Years are always modelled as 365 days long, hence (n 365 / days_per_timestep) is always the beginning of the n-th year of the intervention period (excepting above offset).
The ageGroup
element describes which age-groups human-specific data is segregated into. Examples:
<ageGroup lowerbound="0.0">
<group upperbound="0.25"/>
<group upperbound="0.5"/>
<group upperbound="0.75"/>
<group upperbound="1"/>
<group upperbound="1.5"/>
<group upperbound="2"/>
<group upperbound="3"/>
<group upperbound="4"/>
<group upperbound="5"/>
<group upperbound="6"/>
<group upperbound="7"/>
<group upperbound="8"/>
<group upperbound="9"/>
<group upperbound="10"/>
<group upperbound="12"/>
<group upperbound="14"/>
<group upperbound="16"/>
<group upperbound="18"/>
<group upperbound="20"/>
<group upperbound="25"/>
<group upperbound="30"/>
<group upperbound="35"/>
<group upperbound="40"/>
<group upperbound="45"/>
<group upperbound="50"/>
<group upperbound="55"/>
<group upperbound="60"/>
<group upperbound="65"/>
<group upperbound="70"/>
<group upperbound="99"/>
</ageGroup>
<ageGroup lowerbound="0.0">
<group upperbound="99"/>
</ageGroup>
Here the upper bound is inclusive, so exact age 1 is included under age group 4 (with upper bound 1), but exact age 0 is always included in the first age group. Note also that this is no implicit catch-all last age group, so if the upper bound on the last age group is less than the oldest age allowed, then humans who are older than the last upper bound will simply not be included in surveys.
By default, survey data comes from the whole simulated population. It is also possible to specify monitoring only for defined subpopulations.
Whereas survey reporting is designed to aggregate data into configurable-size lumps, the continuous reporting mechanism is designed to report some data at high frequencies (but generally without segregation by age group and with less configuration potential).
To enable continuous reporting, add a continuous
sub-element to the monitoring
element, of the following form.
<continuous duringInit="false" period="1">
<option name="input EIR" value="true"/>
<option name="simulated EIR" value="true"/>
<option name="human infectiousness" value="true"/>
</continuous>
The period
attribute specifies the number of time-steps between reports. duringInit
is mostly used for debugging and can be omitted entirely; if set to true it enables reporting during the warm-up period and an extra column in the output (simulation time, the time-step counting from the beginning of the simulation rather than the beginning of the intervention period).
A list of available continuous outputs is here.
As of schema 32, multiple subpopulations may be monitored in surveys (but not in continuous output).
Each of the monitored subpopulations must first be defined, either implicitly, by an intervention within the element, or explicitly by the recruitment only pseudo-intervention.
Each of the subpopulations needs to be specified in the "cohorts" element, which links a subpopulation number
to the id
assigned when the subpopulation was declared in the "component" element:
<cohorts>
<subPop id="StudycohortA" number="1"/>
<subPop id="StudycohortB" number="2"/>
<subPop id="StudycohortB" number="4"/>
....
</cohorts>
The number
must be a power of 2 (i.e. 1, 2, 4, 8, ...). These numbers are used to label the output in the output.txt file.
If only a single subpopulation is listed, Output the corresponding output set in the output.txt file is identified by multiplying this number by 1000. This increment
is then added to the values in the column usually reserved for age Group, corresponding to this subpopulation. The values for the complementary sub-poulation (those not included) retain the standard values in the age-group column.
Where multiple sub-populations are listed, output is segregated according to all combinations of membership: e.g.
if sub-populations A (number=1
) and B (number=2
) are listed, there will be outputs for "member of A and B"(increment
=3000); "member of A but not B"(increment
=1000);, "B but not A"(increment
=2000); and "not a member of A or B"(increment
=0). A corresponding rule is used to assign increment
values to all 8 combinations if three sub-populations are listed (each is further segregated by age groups, survey times and enabled output measures, which could lead to excessive program memory usage and output file size if many subpopulations are listed).
Each of the 2^n output sets is identified by a number: the output set is the output from humans who are members in some set of sub-populations (S1, S2, ...) and not members in some others (T1, T2, ...); the number identifying the set is the sum of the numbers identifying the sets S1, S2, etc.
To monitor a defined cohort only, in Versions before 32, the cohortOnly
is set to "true" as follows:
<monitoring name="(some description or name)" cohortOnly="true">
<continuous ... />
<SurveyOptions ... />
<surveys ... />
<ageGroup ... />
</monitoring>
cohortOnly
works only for versions up to 31 and has been removed in schema version 32. It is used where output is required only for a specific sub-population. This may be assigned values true
or false
or, if not using cohorts, omitted entirely.
If cohortOnly
is set to true
, then the output of most measures are restricted to the cohort (although not quite all; see the list of measures for details); if it is set to false
or omitted, then these measures act on the entire simulated population. To obtain outputs for both the cohort and the entire population prior to version 32 the simulation must be run twice.
Surveys are periodic summaries at predefined time-steps. At those time-steps, information is saved about the quantity of interest, this could be a measurable quantity such as the EIR, or number of events since the last survey time point. Where this data concerns humans, it can be segregated into age groups, and can be sampled either across all simulated individuals or from a selected cohort.
Three options exist to allow measuring time-to-first-event:
firstBoutOnly | Remove individuals from the cohort at the start of their first episode (clinical bout) | Intended for measuring time to first episode with active case detection |
---|---|---|
firstTreatmentOnly | Remove individuals from the cohort when they first seek treatment | Intended for measuring time to first episode with passive case detection |
firstInfectionOnly | Remove individuals from the cohort at completion of the first survey in which they present with a patent infection | Intended for measuring time to first infection, using active case detection |
These are enabled by adding an attribute to the monitoring
element, for example (here also enabling cohortOnly
):
<monitoring name="..." cohortOnly="true" firstBoutOnly="true">
...
</monitoring>
| Download openmalaria | Installation instructions | XML Schema Documentation |
XML Schema Version | Program version | master |
develop |
---|---|---|---|
43 | schema-43.0 |
- User Guide
- Compilation Guide
- Developer Guide
- Schema Update Guide
- Scenario Design Guide
- Monitoring Guide
- Changelog
- Schema Documentation
- Human demography
- Levels of transmission
- Parasite dynamics within humans
- P vivax dynamics
- Vector bionomics and transmission to humans
- Mosquito population dynamics
- Clinical (illness) models
- Time in the models