re-register add-in "Clinical"
HI,I accidentally unregistered the add-in "Clinical", and now when I open JMP it goes directly to JMP but not JMP clinical. is there a way to register it back instead of re-install whole JMP clinical?Thanks.Baoyue
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view all learning resourcesHI,I accidentally unregistered the add-in "Clinical", and now when I open JMP it goes directly to JMP but not JMP clinical. is there a way to register it back instead of re-install whole JMP clinical?Thanks.Baoyue
Hi, I'm puzzled by the detection of deleted files by JSL (JMP 16.0.0 on a Mac Big Sur 11.6.8). I created a folder containing 8 files and ran the following script: Names Default To Here( 1 );
TargetDir = Pick Directory();
TargetFiles = Files In Directory( TargetDir );
N_TargetFiles = N items(TargetFiles);
show(N_TargetFiles);
For( i = 1, i <= N Items( TargetFiles ), i++,
sample = Left( TargetF...
I want to predict mortality over 15 years in a cohort of patients. Data is right censored, with a mortality of 7% in 15 years of observation. The data set to derive a prediction model is about 3,500 subjects and 2,000 for external validation. I ran a Cox proportional hazard model, where I identified significant predictors and their Risk ratios, and a parametric survival analysis where significant...
mdivo
I have a question that may require a bit of DOE theoretical background. I am trying to optimize a formulation. Because of the industry that I am in, it is typical to express the entire formulation as a percentage of some base ingredient. For example, if the base ingredient is always 100 and other components are expressed as proportions of the the base ingredient, the formulation {x = 0.1, y = 0.2,...
Specifically I am looking for CCD Temperature and Time.jmp. Anyone of the SAS staff willing to share a copy of this file?
I have a question that may require a bit of DOE theoretical background. I am trying to optimize a formulation. Because of the industry that I am in, it is typical to express the entire formulation as a percentage of some base ingredient. For example, if the base ingredient is always 100 and other components are expressed as proportions of the the base ingredient, the formulation {x = 0.1, y = 0.2,...
Hi,I am trying to replicate formulas that are currently in the attached excel sheet.Where, DSA_Step_Size(dB) = ABS(of delta of :RESULT rows when ATT1 values are decreasing for the same :FREQUENCY value).The formula is in excel sheet if my explanation is confusing. DSA Range(dB) = ABS(of delta of :RESULT rows when ATT1=63 and ATT1=0 for each :FREQUENCY). I am trying to use for loops in the formula....
Hi,I have a data series shown in the screenshot below, and try to select only the data in the range of "x +/- 0.3" with the center at the maximum value of "y".I got an error message "The argument to SelectWhere did not evaluate to true or false, it is [0]..." from the highlighted line, as shown below. What is puzzling is that the last line worked when only 1 condition is applied.What is wrong with...
Hi everyone! Context: I have a process A which is my reference, and I developped a process B which I want to assess its comparability to process A. To do so, I plan to use a TOST (equivalence test) using the process A's 3xSTD (standard deviation) as a treshold. Now, I want to know how many time should I repeat process B to be sure to be able to detect such variation (knowing that a run is a signif...
Hello I am very new to JMP but I would like to check about for validation of chromatographic methods what the correct categorization of the variables should be:For instance UV detector wavelength (would this be discrete numeric?)Column Temperature (continuous)Flow Rate (continuous)Mobile Phase A Buffer concentration (continuous)pH of Mobile Phase A (continuous) Many Thanks James
HI, How to find estimators of FGNLS and NLS (Seemingly Unrelated Regressions) Using JmpPro.# Note that it is present in SAS in the proc syslin
and it is in stat in the nlsur command Regards
Hello, I am trying to do a matched sample analysis across three different factors. I wanted to:1. Confirm that my sample would be what I pick for 'Block" when I do Fit Y by X when running Friedman's test2. Is there a post hoc analysis in JMP that I can use? I dont see Nemenyi or Conover as an optionThanks for your time.
Hello everyone,I am trying to make a table with the OOT (out of Trend) batches with their respective "atypical" values.I used for that the "script alarm" function as I could found some exemples on the JMP community. Here is my script: z_KSigmaZ =1.4;
// Création de la Carte de controle si N catégories > 5
Names Default To Here( 1 );
If(N Items(Associative Array(:"RNS/NS tordu (srg)")) > 5,
Gr...
While taking the Exploratory Data Analysis module, it is time to practice. However, when trying to access the JMP Virtual Lab, I cannot get past the "Create User" option. JMP VIRTUAL LABTo use the Virtual Lab, please select the Create User link below. If you would prefer to use software on your own machine, please select the Download Data link below.
Create User Download Course Data Clicking the C...
Hello. I am trying to use the EMP tool to help set guardbands to my test limits based on my gauge R and R data from a final test machine.I used 10 devices and measured these devices 5 times each, across 5 different test sites on the machine.I need to know how much to guardband my Upper and Lower specs. I am having trouble understanding how to apply the data in the EMP report. I feel like this is a...
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