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All the analyses described in the other vignettes (classification, gene mutant dosage, survival analysis and metastatic pattern analysis) are also available without writing any R code, through the INCOMMON web app:

https://ncalonaci.shinyapps.io/incommon/

The app runs the same underlying INCOMMON model used by this package, and is meant for users who want to explore the method interactively or classify a dataset without setting up an R/cmdstanr environment.

With the app you can, briefly:

  • upload your own genomic_data and clinical_data tables (in the same format expected by init(), see the Get started vignette) or explore the bundled MSK-MetTropism example cohort;
  • run INCOMMON classification of mutation copy number and multiplicity directly from the browser, without installing cmdstanr/Stan locally;
  • browse the resulting genome interpretation (gene mutant dosage classes) and the diagnostic/posterior plots produced by the model;
  • interactively perform survival and metastatic-tropism analyses on the classified cohort;
  • download the classification results and plots for use outside the app.

For full control over the analysis (custom priors, scripting, integration into a larger pipeline), use the R package directly as described in the other vignettes; the app is best suited to quick, exploratory use.