Kermack–McKendrick Epidemic SIR Infectious Disease Model - Metrics by Guy Lakeman

This is a simple SIR infectious diseases 3 stock model with Susceptibles, Infectives and Recovereds stocks. In the initial description the R signified Removed and could include Deaths, Recovered with immunity to infection (Resistant) or those who had fled the epidemic. Note the need to initiate the epidemic by adding a pulse of a single infected person at time 0.

Here we have a basic SEIR model and we will investigate what changes would be appropriate for modelling the 2019 Coronavirus.

The initial parametrization is based on the suggested current data. The initial population is set for Catalonia.

Kermack–McKendrick Epidemic SIR Infectious Disease Model - Metrics by Guy Lakeman

This is a simple SIR infectious diseases 3 stock model with Susceptibles, Infectives and Recovereds stocks. In the initial description the R signified Removed and could include Deaths, Recovered with immunity to infection (Resistant) or those who had fled the epidemic. Note the need to initiate the epidemic by adding a pulse of a single infected person at time 0.

Here we have a basic SEIR model and we will investigate what changes would be appropriate for modelling the 2019 Coronavirus.

We add simple containment meassures that affect two paramenters, the Susceptible population and the rate to become infected.

The initial parametrization is based on the suggested current data. The initial population is set for Catalonia.

The questions that we want to answer in this kind of models are not the shape of the curves, that are almost known from the beginning, but, when this happens, and the amplitude of the shapes. This is crucial, since in the current circumstance implies the collapse of certain resources, not only healthcare.

The validation process hence becomes critical, and allows to estimate the different parameters of the model from the data we obtain. This simulation approach allows to obtain somethings that is crucial to make decisions, the causality. We can infer this from the assumptions that are implicit on the model, and from it we can make decisions to improve the system behavior.

Yes, simulation works with causality and Flows diagrams is one of the techniques we have to draw it graphically, but is not the only one. On https://sdlps.com/projects/documentation/1009 you can review soon the same model but represented in Specification and Description Language.

Here we have a basic SEIR model and we will investigate what changes would be appropriate for modelling the 2019 Coronavirus.

The initial parametrization is based on the suggested current data. The initial population is set for Catalonia.

This model shows the relationship between placement to Bourke Hospital and Infection Rate, Recovery rate and release from Bourke Hospital.  

This insight is about infection propagation and  population migration influence on this propagation. For this, we defined a world population size and a percentage of it who’s infected. Then, we created an agent where we simulated possible states of an individual. So, he can be healthy, infected (with an infection rate) or immunized ( with a certain rate of immunization). If the individual is infected, he can be alive or dead. Then, we simulated different continents (North-America, Asia and Europe) with a migration between these with a certain rate of migration (we tried to approach reality). Then, thanks to our move action which represents a circular permutation between the different continents with a random probability, the agent will be applied to every individual of the world population.

 How does the program work ?

In order to use this insight, we need to define a size of world population and a probability of every individual to reproduce himself. Every individual of this population can have three different state (healthy, infected or immunized) and infected people can be alive or dead. We need to define a percentage of infection for healthy people and a percentage of death for infected people and also a percentage of immunization.
Finally, there is Migration Part of the program, in this one, we need to define three different continents, states or whatever you want. We also need to define a migration probability between each continent to move these person. With this moving people, we can study the influence of migration on the propagation of a disease.

Vincent Cochet, Julien Platel, Jordan Béguet

This insight is about infection propagation and  population migration influence on this propagation. For this, we defined a world population size and a percentage of it who’s infected. Then, we created an agent where we simulated possible states of an individual. So, he can be healthy, infected (with an infection rate) or immunized ( with a certain rate of immunization). If the individual is infected, he can be alive or dead. Then, we simulated different continents (North-America, Asia and Europe) with a migration between these with a certain rate of migration (we tried to approach reality). Then, thanks to our move action which represents a circular permutation between the different continents with a random probability, the agent will be applied to every individual of the world population.

 How does the program work ?

In order to use this insight, we need to define a size of world population and a probability of every individual to reproduce himself. Every individual of this population can have three different state (healthy, infected or immunized) and infected people can be alive or dead. We need to define a percentage of infection for healthy people and a percentage of death for infected people and also a percentage of immunization.
Finally, there is Migration Part of the program, in this one, we need to define three different continents, states or whatever you want. We also need to define a migration probability between each continent to move these person. With this moving people, we can study the influence of migration on the propagation of a disease.

Vincent Cochet, Julien Platel, Jordan Béguet

This insight is about infection propagation and  population migration influence on this propagation. For this, we defined a world population size and a percentage of it who’s infected. Then, we created an agent where we simulated possible states of an individual. So, he can be healthy, infected (with an infection rate) or immunized ( with a certain rate of immunization). If the individual is infected, he can be alive or dead. Then, we simulated different continents (North-America, Asia and Europe) with a migration between these with a certain rate of migration (we tried to approach reality). Then, thanks to our move action which represents a circular permutation between the different continents with a random probability, the agent will be applied to every individual of the world population.

 How does the program work ?

In order to use this insight, we need to define a size of world population and a probability of every individual to reproduce himself. Every individual of this population can have three different state (healthy, infected or immunized) and infected people can be alive or dead. We need to define a percentage of infection for healthy people and a percentage of death for infected people and also a percentage of immunization.
Finally, there is Migration Part of the program, in this one, we need to define three different continents, states or whatever you want. We also need to define a migration probability between each continent to move these person. With this moving people, we can study the influence of migration on the propagation of a disease.

Vincent Cochet, Julien Platel, Jordan Béguet

This insight is about infection propagation and population migration influence on this propagation.

For this, we defined a world population size and a percentage of it who’s infected. Then, we created an agent where we simulated possible states of an individual.

So, he can be healthy, infected (with an infection rate) or immunized ( with a certain rate of immunization). If the individual is infected, he can be alive or dead. Then, we simulated different continents (North-America, Asia and Europe) with a migration between theses with a certain rate of migration (we tried to approach reality).

Then, thanks to our our move action which represent a circular permutation between the different continents with a random probability the agent will be applied to every individual of the world population.

How the program works ?

In order to use this insight needs to define a size of world population and a probability of every individual to reproduce himself.

Every individual of this population can have three different state (healthy, infected or immunized) and infected people can be alive or dead.

We need to define a percentage of infection to healthy people and a percentage of death for infected people and also a percentage of immunization.

Finally there is le migration part of the program, in this one we need to define three different continents, states or whatever you want. We also need to define a migration probability between each continent to move these person.

With this moving people we can study the influence of migration on the propagation of a disease.

If you include zombie disease and zombie cannibalism, how long would a zombie apocalypse last?

Here we have a basic SEIR model and we will investigate what changes would be appropriate for modelling the 2019 Coronavirus.

The initial parametrization is based on the suggested current data. The initial population is set for Catalonia.

Here we have a basic SEIR model and we will investigate what changes would be appropriate for modelling the 2019 Coronavirus.

The initial parametrization is based on the suggested current data. The initial population is set for Catalonia.

Upgrade of Kermack–McKendrick Epidemic SIR Infectious Disease Model (circa 2015) - Metrics by Guy Lakeman

This is a simple SIR infectious diseases 3 stock model with Susceptibles, Infectives and Recovereds stocks. In the initial description the R signified Removed and could include Deaths, Recovered with immunity to infection (Resistant) or those who had fled the epidemic. Note the need to initiate the epidemic by adding a pulse of a single infected person at time 0.

Addition of a slider for susceptibles is equivalent to accumulated total cases

SARS, MERS AND COVID are similar virus types only differing in their sub genus

The COVID outbreak has reached 150,000 infected people

This simulation allows an attempt at predicting how long the virus will persist and its longevity dependence on its high speed massive infection numbers that have reached pandemic proportions

SARS reached 8,000 infected total and ran for 9 months before stopping

MERS 2012 is still killing 8 years later with patients dying even after using interferon to try and cure them

SARS-CoV-19 spread in different countries

Here we have a basic SEIR model and we will investigate what changes would be appropriate for modelling the 2019 Coronavirus.

The initial parametrization is based on the suggested current data. The initial population is set for Catalonia.

Upgrade of Kermack–McKendrick Epidemic SIR Infectious Disease Model (circa 2015) - Metrics by Guy Lakeman

This is a simple SIR infectious diseases 3 stock model with Susceptibles, Infectives and Recovereds stocks. In the initial description the R signified Removed and could include Deaths, Recovered with immunity to infection (Resistant) or those who had fled the epidemic. Note the need to initiate the epidemic by adding a pulse of a single infected person at time 0.

Addition of a slider for susceptibles is equivalent to accumulated total cases

SARS, MERS AND COVID are similar virus types only differing in their sub genus

The COVID outbreak has reached 150,000 infected people

This simulation allows an attempt at predicting how long the virus will persist and its longevity dependence on its high speed massive infection numbers that have reached pandemic proportions

SARS reached 8,000 infected total and ran for 9 months before stopping

MERS 2012 is still killing 8 years later with patients dying even after using interferon to try and cure them

Upgrade of Kermack–McKendrick Epidemic SIR Infectious Disease Model (circa 2015) - Metrics by Guy Lakeman

This is a simple SIR infectious diseases 3 stock model with Susceptibles, Infectives and Recovereds stocks. In the initial description the R signified Removed and could include Deaths, Recovered with immunity to infection (Resistant) or those who had fled the epidemic. Note the need to initiate the epidemic by adding a pulse of a single infected person at time 0.

Addition of a slider for susceptibles is equivalent to accumulated total cases

SARS, MERS AND COVID are similar virus types only differing in their sub genus

The COVID outbreak has reached 150,000 infected people

This simulation allows an attempt at predicting how long the virus will persist and its longevity dependence on its high speed massive infection numbers that have reached pandemic proportions

SARS reached 8,000 infected total and ran for 9 months before stopping

MERS 2012 is still killing 8 years later with patients dying even after using interferon to try and cure them

SARS-CoV-19 spread in different countries

Here we have a basic SEIR model and we will investigate what changes would be appropriate for modelling the 2019 Coronavirus 

Here we have a basic SEIR model and we will investigate what changes would be appropriate for modelling the 2019 Coronavirus.

The initial parametrization is based on the suggested current data. The initial population is set for Catalonia.

Here we have a basic SEIR model and we will investigate what changes would be appropriate for modelling the 2019 Coronavirus