ylg | CVPR 2020 ] Official Implementation | Machine Learning library
kandi X-RAY | ylg Summary
kandi X-RAY | ylg Summary
[CVPR 2020] Official Implementation: "Your Local GAN: Designing Two Dimensional Local Attention Mechanisms for Generative Models".
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Top functions reviewed by kandi - BETA
- Creates training and validation inputs
- Returns a function that preprocesses the dataset record records
- Provide a dataset
- Makes a random tensor
- Run train and write images
- Writes the image to disk
- Log performance statistics
- Predict and write images to disk
- Get x and y coordinates
- Get the list of nearest neighbors
- Visualize attention
- Calculate saliency weights
- Samples a nonlocal block
- 1x1d convolutional convolution layer
- Get real activations
- Get activations from a dataset
- Inject weights into model_vars
- Assign two lists
- Provides training data
- Run training
- Run continuous evaluation
- Get a 2D grid mask
- Computes the discriminator loss
- Returns a list of the lookups and fast weights
- Interpolate between two points
- Generate a repetitive mask for the given nL
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QUESTION
I have a model with 10 equations that describe a fed-batch bioreactor. Basically, every 24h "food" (Glucose and other components) is added to the system. My problem is that this feeding procedure is currently being modeled as the flow-rate (L/H) over two time steps (delta_T), instead of a single discrete food addition (delta_T = 0).
This is what the glucose equation looks like:
...ANSWER
Answered 2019-Dec-19 at 06:36Your strategy to feed glucose as a pulse is a good method to have a discontinuous input. The problem with a discrete jump in glucose concentration is that there is a glucose derivative term as equation 4: m.Equation(G.dt() == e4)
. If the dG/dt
term changes over a very short amount of time then the derivative term gets very large.
One strategy to deal with the large derivatives at discrete points is to use m.options.NODES=2
to avoid problems with the additional internal nodes with orthogonal collocation on finite elements. With no internal nodes, you may need to increase the number of time points to maintain accuracy for the integration. This allows a very short-duration impulse input of glucose to the batch reactor such as 3.6 seconds
for the addition.
feed_small_delta_t = 0.001 # 3.6 seconds
The index for the feed input is off by one so Fi[i+1]
should be where the impulse is applied, not Fi[i]
.
QUESTION
I am new to GEKKO and also to modeling bioreactors, so I might be missing something obvious.
I have a system of 10 ODEs that describe a fed-batch bioreactor. All constants are given. The picture below shows the expected behavior of this model (extracted from a paper). However, the only feasible solution I found is when Viable Cells Density (XV) = 0, and stays 0 for all time t, or if time T is really small (<20). If a lower boundary >= 0 or initial value is set to XV and t > 20, the system becomes infeasible.
Equations and constants were checked multiple times. I tried giving initial values to my variables, but it didn't work either. I can only think of two problems: I am not initiating variables properly, or I am not using GEKKO properly. Any ideas? Thanks!!
...ANSWER
Answered 2019-Dec-10 at 23:16In the end it is not a programming problem, but a problem reading the equations and correctly translating them.
mu
and Kd
are not dynamical variables, they are ordinary functions of the state vector (which then only has dimension 8). For such intermediate variables Gekko has the construction function m.Intermediate
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