Time in hh:mm but plots in seconds
I have time column with hh:mm data, however during analysis few plots show axis in seconds and few in hh:mm. How JMP decides what to use/display and how do I ensure output with consistent format?
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view all learning resourcesI have time column with hh:mm data, however during analysis few plots show axis in seconds and few in hh:mm. How JMP decides what to use/display and how do I ensure output with consistent format?
I'd like to retrieve the current month's name to display it in my results.
I tried using this function but i get every time the current date in format dd/mm/yyyy :
current_month = Format(Today(), "Mon");
textbox_result << Set Text(
"ICT NOK % for " || current_month || " is " || Char(Round(percent_nok_ict, 2)) || "%\!N" ||
"FCT NOK % for " || current_month || " is " || Char(Ro...
As the title states, I found differences in the result segments when performing density analysis. For example as the follows image, the orange data is not at a high point in "Compare of density", but it is the highest in "Composition of densities". Hope someone can help explain this reason, what is the operational difference between these two methods?
For example, this folder:C:\Windows
Thanks!
I've long used JMP to make box plots to show the distributin of data for a number of field sites on the same axis. I recently upgraded to JMP 14 and now the axis look different than they have in the past. Specifically, I'm running into an issue where the axis seems homogenized regardless of where the actual outliers are. For instance, in the old format if the outlier was 20000 then it would plot 4...
I have time column with hh:mm data, however during analysis few plots show axis in seconds and few in hh:mm. How JMP decides what to use/display and how do I ensure output with consistent format?
As the title states, I found differences in the result segments when performing density analysis. For example as the follows image, the orange data is not at a high point in "Compare of density", but it is the highest in "Composition of densities". Hope someone can help explain this reason, what is the operational difference between these two methods?
For example, this folder:C:\Windows
Thanks!
Hello, I ran a DOE on JMP 17, and I am beginning to parse the data with JMP using the effect summary. It is a four-component mixture. I've watched some videos in the JMP catalogue on using the effect summary for mixtures and been following what they've been doing (removing sources that had a P value >0.05, if it doesn't have any dependencies above it). Are there any circumstances, that I would dev...
Hello,I used the Local Kernel Smoother (Tri-Cubic) with linear connector for my ordinal x-axis scale.Now I need to report the methodology and calculation approach within my pharmaceutical compliance report.I could not find in the instruction's manual how the bandwidth was calculated or other details.Could someone give me the exact approach JMP 17.2 is using for as described in my first sentence? ...
Setup : JMP 17.0.0 on Win11.I create boxplots and export to HTML (default graphics format = SVG).
On line 16 of the html file, there is an autogenerated link to adobe :pluginspage="http://www.adobe.com/svg/viewer/install/"This webpage doesn't exist and I think the Adobe SVG Viewer is not available anymore, so the above link should be removed.https://web.archive.org/web/20121221000422/http://www.ado...
Hello, I am conducting a two-way ANOVA with a random effect and need to report the partial eta squared. Does anyone know how to do this or calculate it from values displayed in the output? I tried the add-on but it does not support models with random effects. For the model I have a dependent variable and my model effects looks like:variable1variable2variable1*variable2variable3 & random all variab...
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 ...
Hello everyone, I am currently analyzing "Agreement within Raters" and would like to better understand how these confidence intervals are calculated. My main questions are:What steps or methods are used to calculate confidence intervals in "Agreement within Raters" of Attributive analyses?Which statistical distribution is typically used for these calculations? Could anyone recommend some literatur...
Hi. I want to analyze how well two biomarkers work together in the detection of diseased from healthy and compare the combination to the single markers. I have previously done such analysis in SPSS using binary logistic regression and then simply running ROC-analysis for single markers and combination. With JMP I cannot find how to combine two biomarkers using a logistic regression analysis. Could...
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