Predicted response of ANN
when I save the predicted response of ANN in jmp, it gave me points not values
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view all learning resourceswhen I save the predicted response of ANN in jmp, it gave me points not values
Hi everone I would like to conduct a field trial. I would like to check the response of a new fertilizer (at different levels) with and without exisiting fertilizers on yield of wheat. i need help with DOE. so basically i have eight treatments T0= negative control (no fertlizers), T1= positive control (NPK) business as usual fertlizers, T2= NPK+low level of new fertilizer, T3=NPK+medium level of n...
Hi all, I'm doing a Full factorial DOE with 2 factors & 2 responses. & wondering how doAfter testing & run the model. The result show that there is no significant factors & no significant model also. But Looking at the interaction profiler. I see some clear trends in Factor A & response X.
So my question is how to use this result correctly. - With this, I cannot predict quantitatively by using ...
Hi,I'm looking to qualify new lot of the controls for an assay and was wondering what the best way is to accomplish in JMP (or to determine the sample size/number of experiments) in JMP.Thank you
For instance. If the purpose of a screening design is to (largely) test for main effects w/ as minimal runs as possible - and I want to screen 7 factors w/ a minimal # of runs, why isn't it a good idea to simply change ea of those factors 1 time on 7 runs? If that's not the most efficient way, would running a saturated design w/ 8 runs for 7 factors be the most efficient way to test for main effe...
when I save the predicted response of ANN in jmp, it gave me points not values
Hi everone I would like to conduct a field trial. I would like to check the response of a new fertilizer (at different levels) with and without exisiting fertilizers on yield of wheat. i need help with DOE. so basically i have eight treatments T0= negative control (no fertlizers), T1= positive control (NPK) business as usual fertlizers, T2= NPK+low level of new fertilizer, T3=NPK+medium level of n...
Hi all, I'm doing a Full factorial DOE with 2 factors & 2 responses. & wondering how doAfter testing & run the model. The result show that there is no significant factors & no significant model also. But Looking at the interaction profiler. I see some clear trends in Factor A & response X.
So my question is how to use this result correctly. - With this, I cannot predict quantitatively by using ...
Hello community!!,A question: will it be possible for the profiler to find the best combinations of factors with uncertainty when performing a simulation, which maximize the total utility and minimize the total cost, generating a table of the best combinations found? For example:
Hi All, I am planning an experiment to understand the lifetime of a product. Samples will be cut-out from the product. A batch of product is 15000 and I will cut smaller pieces suitable for bending test. Samples will be stored in different chemicals and there will at least 5 time-periods. I take out after each t1, t2, ... samples out of the solution an test. By this my goal is to fit the degradati...
Hello community!!,A question: will it be possible for the profiler to find the best combinations of factors with uncertainty when performing a simulation, which maximize the total utility and minimize the total cost, generating a table of the best combinations found? For example:
Definitely, JMP is Not a Spreadsheet . And that's great!!
Besides this difference, there are other places where Jmp doesn't do/behave/produce what a newbie / innocent Jmp user expects.
If a user knows these issues and the remedies and workarounds - he/she can
a) save a lot of time
b) be safe from data loss
c) be sure that the results are as expected.
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Hi, I'm working on a dataset where we are testing the effects of 2 treatments and the delay between them, and I'm trying to figure out how to line up my variables so I can do a Dunnett's test against various controls. We are giving animals a dose of drug A (Variable A), waiting some time (T), and then giving them a dose of drug B . If the animal is NOT given drug A (= 0), then T doesn't have a m...
Hi, I designed a DOE that has two independent buffers. This DOE will range components in each buffer which will be used in a processing step sequentially. IE, buffer A, followed by buffer B. We already prepared for the DOE, and formulated the A buffers as per the recommended design. For the B buffers, we intended on ranging 2 components but later decided to reduce to ranging one component, and als...
Hi everyone,I would like to design my first DCE. I am going to use 6 attributes that differ in the levels from 2 to 4 levels. However, I have a limitation where there is an impossible combination that may appear; for example, the cheapest product would not be possible to have the best feature. Is there any way for me to select the prohibited combination? Or, is the D-optimal design will always cal...
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