profileur et indicateur de sensibilité
bonjour, j'ai affiché l'indicateur de sensibilité dans le profileur (triangle mauve)je n'ai pas trouvé des informations dans l'aide. comment interpréter cette information? cordialement
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view all learning resourcesbonjour, j'ai affiché l'indicateur de sensibilité dans le profileur (triangle mauve)je n'ai pas trouvé des informations dans l'aide. comment interpréter cette information? cordialement
I know that I can save the formula to predict the responses but to evaluate the model I need to keep the model statistics, and it changes every time I open the neural report. If someone can provide me with some guidance, I need to be able to open the neural report more than just once.
Good morning,
The aim is to test mixtures of components to target a continuous variable Z.
To achieve this, the blend must contain one (and only one) component from each of the following familly (these categories are made up of components with similar characteristics), plus glycerine (systematically):
Family 1: A, B
Family 2: C, D
Family 3: E, F, G, H, I, J
Family 4: glycerine
Two intermediate continuous...
In the attached JMP file, I built three separate regression models for each response variable weight, turning circle and horsepower with three separate validation columns (Training set = 70%, Validation set = 15%, Training set= 15%).Is it necessary to create validation column for each response variable to build regression models or one validation column with any one response variable is enough?
Hi,I was wondering if there is a platform in JMP17 that helps with 4PL or 5PL curve fitting (for bioassay). I'm looking for a step-by-step guideline as I've never done relative potency analysis with JMP in the past.Thank you
I know that I can save the formula to predict the responses but to evaluate the model I need to keep the model statistics, and it changes every time I open the neural report. If someone can provide me with some guidance, I need to be able to open the neural report more than just once.
Good morning,
The aim is to test mixtures of components to target a continuous variable Z.
To achieve this, the blend must contain one (and only one) component from each of the following familly (these categories are made up of components with similar characteristics), plus glycerine (systematically):
Family 1: A, B
Family 2: C, D
Family 3: E, F, G, H, I, J
Family 4: glycerine
Two intermediate continuous...
Hi,I was wondering if there is a platform in JMP17 that helps with 4PL or 5PL curve fitting (for bioassay). I'm looking for a step-by-step guideline as I've never done relative potency analysis with JMP in the past.Thank you
Hi, I have done a finite element model validation study by comparing the a certain quantity of interest to experimental data. I have conducted this study for 18 different samples in order to evaluate the mean prediction error of the model. The real & simulated samples are dependent. I want to assess if 18 was a statistically significant number of samples. How can i calculate the power? Thanks for...
Dear Sir/Madam,I am a consultant for research development, engineering, product development, and manufacture of chemicals, biochemicals, pharmaceutical drugs, supplements, fertilizers, pesticides, health products, CHIPS, Substrates, PCBs, and construction products for the Biotech, Pharmeceutical, Microelectronic, Agriculture, Farming, clinical trials, food, and other general manufacturing.The work...
I have used the interval explorer for parametric reliability life test planning for sample size calculation of accelerated life test. Please can someone confirm if the sample size returned is the total sample size or sample size per stress levels? Assuming I have 3 temperature levels, do I use 75 samples per temperature level or 25?
Hello Community!Attached is the script "Hogi chart calculates risk and probability", an excellent work by HOGI ... which calculates the risks and probabilities of occurrence of an input or multiple inputs (x), of an output or multiple outputs (Y) or their combination in a table. For example:Would it be possible to expand the capacity of the script to make a sensitivity analysis of the inputs (x) o...
Hi, I have a multinomial logistic regression of 3 classes: 0, 1, and 2 and have associated individual models (via Fit Y by X) for N parameters. I am now looking into a sensitivity like study in which each parameter is assumed at certain levels (e.g. at min, max etc..). I have probabilities computed at each such parameter level. I like to rank order probability change in each class (0, 1 and 2) du...
Dear JMP community,I am presented with a problem of building a model using over-dispersed zero-inflated count data. I hope you can help me with this.I have attached both training and validation datasets to this post. My objective is to build my model on the training dataset and validate it using the validation dataset. I have not worked with such count data before and therefore do not know validat...
Hello,I'm trying to reproduce the results obtained on JMP with the "Neural" model by adding nested cross-validation, which is not possible on the software. However, the architecture is very unclear and I can't understand the calculations performed by the model. I don't have access to certain information such as batch size, optimizer used, loss, learning rate (except the one for the boosting), and ...
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