# Modeling spatially resolved omics with mistyR

Jovan Tanevski1,2*

1Heidelberg University and Heidelberg University Hospital, Heidelberg, Germany
2Jožef Stefan Institute, Ljubljana, Slovenia

*jovan.tanevski@uni-heidelberg.de

#### 2025-04-15

#### Package

mistyR 1.16.0

# 1 Introduction

The use of mistyR is conceptualized around building a workflow for analysis of spatial omics data by four classes of functions:

- View composition

- Model training

- Result processing

- Plotting

To construct a workflow mistyR is designed with the use of pipe operators (for example the operator `%>%` from magrittr) for chaining functions in mind.

When loading mistyR please consider configuring a `future::multisession()` parallel execution plan. mistyR will then use all available cores for execution of computationally demanding functions. It is recommended that the user modifies the `future::plan()` according to their needs.

    # MISTy
    library(mistyR)
    library(future)

    # data manipulation
    library(dplyr)
    library(purrr)
    library(distances)

    # plotting
    library(ggplot2)

    plan(multisession)

The following example uses the synthetically generated benchmark data `synthetic` that is included in the package. The dataset is a list of 10 tibbles, each representing data generated from a random layout of four cell types and empty space on a 100-by-100 grid.

The data was generated by simulating a two-dimensional cellular automata model that focuses on signaling events. The model simulates the production, diffusion, degradation and interactions of 11 molecular species. Note that the dataset contains simulated measurements only for the non-empty spaces.

    data("synthetic")

    ggplot(synthetic[[1]], aes(x = col, y = row, color = type)) +
      geom_point(shape = 15, size = 0.7) +
      scale_color_manual(values = c("#e9eed3", "#dcc38d", "#c9e2ad", "#a6bab6")) +
      theme_void()

    str(synthetic[[1]], give.attr = FALSE)
    #> spc_tbl_ [4,205 × 14] (S3: spec_tbl_df/tbl_df/tbl/data.frame)
    #>  $ row  : num [1:4205] 1 1 1 1 1 1 1 1 1 1 ...
    #>  $ col  : num [1:4205] 100 11 13 14 15 20 23 24 26 32 ...
    #>  $ ECM  : num [1:4205] 0.0385 0.0327 0.1444 0.387 0.1635 ...
    #>  $ ligA : num [1:4205] 0.834 0.119 0.525 0.269 0.195 ...
    #>  $ ligB : num [1:4205] 0.0157 0.0104 0.014 0.0367 0.1176 ...
    #>  $ ligC : num [1:4205] 0.236 0.804 0.334 0.502 0.232 ...
    #>  $ ligD : num [1:4205] 1.183 0.101 0.434 0.241 0.203 ...
    #>  $ protE: num [1:4205] 1.18 0 1.67 0 0 ...
    #>  $ protF: num [1:4205] 2.547 0.386 1.614 0.913 0.162 ...
    #>  $ prodA: num [1:4205] 0.382 0 0.472 0 0 ...
    #>  $ prodB: num [1:4205] 0 0 0 0 0.16 ...
    #>  $ prodC: num [1:4205] 0 0.536 0 0.418 0 ...
    #>  $ prodD: num [1:4205] 0.588 0 0.379 0 0 ...
    #>  $ type : chr [1:4205] "CT1" "CT2" "CT1" "CT2" ...

For more information about the underlying model and data generation see `help(synthetic)` or the publication.

# 2 View composition

The mistyR workflow always starts by defining an intraview (`create_initial_view()`) containing measurements of the markers that are the target of the modeling at each cell of interest. For the first sample from the `synthetic` dataset we select all markers except for the ligands for all available cells.

    expr <- synthetic[[1]] %>% select(-c(row, col, type, starts_with("lig")))

    misty.intra <- create_initial_view(expr)

    summary(misty.intra)
    #>                Length Class  Mode
    #> intraview      2      -none- list
    #> misty.uniqueid 1      -none- character
    summary(misty.intra$intraview)
    #>        Length Class       Mode
    #> abbrev 1      -none-      character
    #> data   7      spec_tbl_df list

From the intrinsic view (intraview)1 1 1 You will notice that `misty.intra` contains an element named `misty.uniqueid` that is used for caching. If not provided, this id is automatically generated. mistyR will model the expression of each marker as a function of the expression of other markers within the cell. We are interested in exploring marker expressions coming from different spatial contexts that are complementary, i.e., that are distinguishable and contribute to the explanation of the overall expression of the markers.

mistyR includes two default helper functions for calculating and adding views that take into account the spatial context of the data: `add_juxtaview()` and `add_paraview()`. The juxtaview represent a local spatial view and captures the expression of all markers available in the intraview within the immediate neighborhood of each cell. The paraview captures the expression of all markers avainalbe in the intraview in the boarder tissue structure where the importance of the influence is proportional to the inverse of the distance between two cells. To add a paraview in the view composition, we first need information about the location of each cell from the intraview. Using this information we can create and add a paraview with importance radius of 10 to the view composition.

    pos <- synthetic[[1]] %>% select(row, col)

    misty.views <- misty.intra %>% add_paraview(pos, l = 10)
    #>
    #> Generating paraview

    summary(misty.views)
    #>                Length Class  Mode
    #> intraview      2      -none- list
    #> misty.uniqueid 1      -none- character
    #> paraview.10    2      -none- list

The calculation of a juxtaview and a paraview can be computationally intensive when there are a large number of cells in the sample. Therefore the calculation is run in parallel with the set `future::plan()`. The computational time needed for the calculation of the paraview can also be significantly reduced by approximation. Refer to the documentation of this function (`help(add_paraview)`) for more details.

Other relevant and custom views can be created (`create_view()`) from an external resource (`data.frame`, `tibble`) and added to the view composition. The data should contain and one row per cell in order as in the intraview. For example we can create a view that captures the mean expression of the 10 nearest neighbors of each cell.

    # find the 10 nearest neighbors
    neighbors <- nearest_neighbor_search(distances(as.matrix(pos)), k = 11)[-1, ]

    # calculate the mean expression of the nearest neighbors for all markers
    # for each cell in expr
    nnexpr <- seq_len(nrow(expr)) %>%
      map_dfr(~ expr %>%
        slice(neighbors[, .x]) %>%
        colMeans())

    nn.view <- create_view("nearest", nnexpr, "nn")

    nn.view
    #> $nearest
    #> $nearest$abbrev
    #> [1] "nn"
    #>
    #> $nearest$data
    #> # A tibble: 4,205 × 7
    #>      ECM protE protF  prodA  prodB  prodC  prodD
    #>    <dbl> <dbl> <dbl>  <dbl>  <dbl>  <dbl>  <dbl>
    #>  1 0.169 0.337 1.07  0.120  0.0138 0.146  0.165
    #>  2 0.346 0.676 0.549 0.0969 0.0140 0.190  0.0766
    #>  3 0.219 0.304 0.495 0.0496 0.0288 0.236  0.0387
    #>  4 0.238 0.607 0.651 0.132  0.0288 0.0954 0.122
    #>  5 0.313 0.688 0.835 0.166  0.0297 0.0837 0.173
    #>  6 0.527 0.743 0.616 0.0722 0.0184 0.135  0.0964
    #>  7 0.278 0.399 0.501 0.0413 0.0632 0.160  0.0604
    #>  8 0.266 0.537 0.624 0.0738 0.0463 0.154  0.117
    #>  9 0.356 0.564 0.565 0.0696 0.0415 0.208  0.106
    #> 10 0.625 0.863 0.458 0.0350 0.0823 0.230  0.0576
    #> # ℹ 4,195 more rows

The created view(s) can be added (`add_views()`) to an existing view composition one by one or by providing them in a form of a list. Other examples of creating and adding custom views to the composition can be found in the resources in See also.

    extended.views <- misty.views %>% add_views(nn.view)

    summary(extended.views)
    #>                Length Class  Mode
    #> intraview      2      -none- list
    #> misty.uniqueid 1      -none- character
    #> paraview.10    2      -none- list
    #> nearest        2      -none- list

Views can also be removed from the composition by providing one or more names of views to `remove_views()`. The intraview and misty.uniqueid cannot be removed with this function.

    extended.views %>%
      remove_views("nearest") %>%
      summary()
    #>                Length Class  Mode
    #> intraview      2      -none- list
    #> misty.uniqueid 1      -none- character
    #> paraview.10    2      -none- list

    extended.views %>%
      remove_views("intraview") %>%
      summary()
    #>                Length Class  Mode
    #> intraview      2      -none- list
    #> misty.uniqueid 1      -none- character
    #> paraview.10    2      -none- list
    #> nearest        2      -none- list

# 3 Model training

Once the view composition is created, the model training is managed by the function `run_misty()`. By default, models are trained for each marker available in the intraview for each view independently. The results of the model training will be stored in a folder named “results”.

    misty.views %>% run_misty()
    #>
    #> Training models
    #> [1] "E:/biocbuild/bbs-3.21-bioc/tmpdir/RtmpGuwWXg/Rbuild141a0199d197a/mistyR/vignettes/results"

The workflow that we used for the first sample from the `synthetic` dataset can be easily extended to be applied to all 10 samples to completely reproduce one of the results reported in the publication. The results for each sample will be stored in a subfolder of the folder “results”.

    result.folders <- synthetic %>% imap_chr(function(sample, name) {
      sample.expr <- sample %>% select(-c(row, col, type, starts_with("lig")))
      sample.pos <- sample %>% select(row, col)

      create_initial_view(sample.expr) %>% add_paraview(sample.pos, l = 10) %>%
        run_misty(results.folder = paste0("results", .Platform$file.sep, name))
    })
    #>
    #> Generating paraview
    #>
    #> Training models
    #>
    #> Generating paraview
    #>
    #> Training models
    #>
    #> Generating paraview
    #>
    #> Training models
    #>
    #> Generating paraview
    #>
    #> Training models
    #>
    #> Generating paraview
    #>
    #> Training models
    #>
    #> Generating paraview
    #>
    #> Training models
    #>
    #> Generating paraview
    #>
    #> Training models
    #>
    #> Generating paraview
    #>
    #> Training models
    #>
    #> Generating paraview
    #>
    #> Training models
    #>
    #> Generating paraview
    #>
    #> Training models

    result.folders
    #>                                                                                              synthetic1
    #>  "E:/biocbuild/bbs-3.21-bioc/tmpdir/RtmpGuwWXg/Rbuild141a0199d197a/mistyR/vignettes/results/synthetic1"
    #>                                                                                             synthetic10
    #> "E:/biocbuild/bbs-3.21-bioc/tmpdir/RtmpGuwWXg/Rbuild141a0199d197a/mistyR/vignettes/results/synthetic10"
    #>                                                                                              synthetic2
    #>  "E:/biocbuild/bbs-3.21-bioc/tmpdir/RtmpGuwWXg/Rbuild141a0199d197a/mistyR/vignettes/results/synthetic2"
    #>                                                                                              synthetic3
    #>  "E:/biocbuild/bbs-3.21-bioc/tmpdir/RtmpGuwWXg/Rbuild141a0199d197a/mistyR/vignettes/results/synthetic3"
    #>                                                                                              synthetic4
    #>  "E:/biocbuild/bbs-3.21-bioc/tmpdir/RtmpGuwWXg/Rbuild141a0199d197a/mistyR/vignettes/results/synthetic4"
    #>                                                                                              synthetic5
    #>  "E:/biocbuild/bbs-3.21-bioc/tmpdir/RtmpGuwWXg/Rbuild141a0199d197a/mistyR/vignettes/results/synthetic5"
    #>                                                                                              synthetic6
    #>  "E:/biocbuild/bbs-3.21-bioc/tmpdir/RtmpGuwWXg/Rbuild141a0199d197a/mistyR/vignettes/results/synthetic6"
    #>                                                                                              synthetic7
    #>  "E:/biocbuild/bbs-3.21-bioc/tmpdir/RtmpGuwWXg/Rbuild141a0199d197a/mistyR/vignettes/results/synthetic7"
    #>                                                                                              synthetic8
    #>  "E:/biocbuild/bbs-3.21-bioc/tmpdir/RtmpGuwWXg/Rbuild141a0199d197a/mistyR/vignettes/results/synthetic8"
    #>                                                                                              synthetic9
    #>  "E:/biocbuild/bbs-3.21-bioc/tmpdir/RtmpGuwWXg/Rbuild141a0199d197a/mistyR/vignettes/results/synthetic9"

Note that by default, mistyR caches calculated views2 2 2 juxtaview and paraview calculated and added by `add_juxtaview()` and `add_paraview()` respectively and trained models, such that in case of repeated running of the workflow they will be retrieved instead of recalculated, thus saving significant computational time. However, the size of the generated cache files can be large. Therefore, the functions that can work with cached files, such as `run_misty()`, have parameter named `cached` that can be set to `FALSE`. Additionally the function `clear_cache()` provides means to remove cache files.

# 4 Result processing

The raw mistyR results are stored in several text files in the output folder for each analyzed sample. The results from one or more samples can be collected, aggregated and coverted to an R object with the function `collect_results()`, by providing path(s) to folder(s) containing results generated by `run_misty()`.

    misty.results <- collect_results(result.folders)
    #>
    #> Collecting improvements
    #>
    #> Collecting contributions
    #>
    #> Collecting importances
    #>
    #> Aggregating

    summary(misty.results)
    #>                        Length Class  Mode
    #> improvements           4      tbl_df list
    #> contributions          4      tbl_df list
    #> importances            5      tbl_df list
    #> improvements.stats     5      tbl_df list
    #> contributions.stats    6      tbl_df list
    #> importances.aggregated 5      tbl_df list

See `help(collect_results)` for more information on the structure of `misty.results`.

# 5 Plotting

MISTy gives explanatory answers to three general questions. Each question can be answered by looking at the corresponding plot.

1. How much can the broader spatial context explain the expression of markers (in contrast to the intraview)?

This can be observed in the gain in R2 (absolute percentage) (or relative percentage of decrease RMSE) of using the multiview model in contrast to the single intraview only model.

    misty.results %>%
      plot_improvement_stats("gain.R2") %>%
      plot_improvement_stats("gain.RMSE")

We can further inspect the significance of the gain in variance explained, by the assigned p-value of improvement based on cross-validation.

    misty.results$improvements %>%
      filter(measure == "p.R2") %>%
      group_by(target) %>%
      summarize(mean.p = mean(value)) %>%
      arrange(mean.p)

target | mean.p
--- | ---
ECM | 0.0184012
protF | 0.0496408
protE | 0.4209367
prodA | 0.4600104
prodB | 0.4985316
prodC | 0.5034351
prodD | 0.5054532

In general, the significant gain in R2 can be interpreted as the following:

“We can better explain the expression of marker X, when we consider additional views, other than the intrinsic view.”

2.How much do different view components contribute to explaining the expression?

    misty.results %>% plot_view_contributions()

As expected most of the contribution to the prediction of the expression of the markers comes from the intraview. However for the markers that we observed significant improvement of variance we can also observe a proportional estimated contribution of the paraview.

3.What are the specific relations that can explain the contributions?

To explain the contributions, we can visualize the importances of markers coming from each view separately as predictors of the expression of all markers.

First, the intraview importances.

    misty.results %>% plot_interaction_heatmap(view = "intra", cutoff = 0.8)

These importances are associated to the relationship between markers in the same cell. As we didn’t use the information about the cell types in any way during the process of modeling the significant interactions that we see in the heatmap may come from any of the cell types.

Second, the paraview importances.

    misty.results %>% plot_interaction_heatmap(view = "para.10", cutoff = 0.5)

These importances are associated to the relationship between markers in the cell and markers in the broader structure (controlled by our parameter l).

We can observe that some interactions in the paraview might be redundant, i.e., they are also found to be important in the intraview. To focus on the interactions coming from the paraview only we can plot the contrast between these results.

    misty.results %>% plot_contrast_heatmap("intra", "para.10", cutoff = 0.5)
    #> Warning: Specifying the `id_cols` argument by position was deprecated in tidyr 1.3.0.
    #> ℹ Please explicitly name `id_cols`, like `id_cols = -c(view, nsamples)`.
    #> ℹ The deprecated feature was likely used in the mistyR package.
    #>   Please report the issue at <https://github.com/saezlab/mistyR/issues>.
    #> This warning is displayed once every 8 hours.
    #> Call `lifecycle::last_lifecycle_warnings()` to see where this warning was
    #> generated.

Futhermore, since the predictor and target markers in both views are the same, we can plot the interaction communities that can be extracted from the estimated interaction pairs from the intraview

    misty.results %>% plot_interaction_communities("intra")

and the paraview.

    misty.results %>% plot_interaction_communities("para.10", cutoff = 0.5)

When interpreting the results and the plots it is important to note that the relationships captured in the importances are not to assumed or interpreted as linear or casual. Furthermore, the estimated importance of a single predictor - marker pair should not be interpreted in isolation but in the context of the other predictors, since training MISTy models is multivariate predictive task.

# See also

## More examples

`browseVignettes("mistyR")`

Online articles

## Publication

Jovan Tanevski, Ricardo Omar Ramirez Flores, Attila Gabor, Denis Schapiro, Julio Saez-Rodriguez. Explainable multiview framework for dissecting spatial relationships from highly multiplexed data. Genome Biology 23, 97 (2022). https://doi.org/10.1186/s13059-022-02663-5

# Session info

Here is the output of `sessionInfo()` at the point when this document was compiled:

    #> R version 4.5.0 RC (2025-04-04 r88126 ucrt)
    #> Platform: x86_64-w64-mingw32/x64
    #> Running under: Windows Server 2022 x64 (build 20348)
    #>
    #> Matrix products: default
    #>   LAPACK version 3.12.1
    #>
    #> locale:
    #> [1] LC_COLLATE=C
    #> [2] LC_CTYPE=English_United States.utf8
    #> [3] LC_MONETARY=English_United States.utf8
    #> [4] LC_NUMERIC=C
    #> [5] LC_TIME=English_United States.utf8
    #>
    #> time zone: America/New_York
    #> tzcode source: internal
    #>
    #> attached base packages:
    #> [1] stats     graphics  grDevices utils     datasets  methods   base
    #>
    #> other attached packages:
    #> [1] ggplot2_3.5.2    distances_0.1.12 purrr_1.0.4      dplyr_1.1.4
    #> [5] future_1.40.0    mistyR_1.16.0    BiocStyle_2.36.0
    #>
    #> loaded via a namespace (and not attached):
    #>  [1] tidyr_1.3.1         sass_0.4.10         generics_0.1.3
    #>  [4] stringi_1.8.7       listenv_0.9.1       digest_0.6.37
    #>  [7] magrittr_2.0.3      RColorBrewer_1.1-3  evaluate_1.0.3
    #> [10] grid_4.5.0          bookdown_0.43       fastmap_1.2.0
    #> [13] R.oo_1.27.0         jsonlite_2.0.0      R.utils_2.13.0
    #> [16] tinytex_0.57        BiocManager_1.30.25 scales_1.3.0
    #> [19] codetools_0.2-20    jquerylib_0.1.4     rlist_0.4.6.2
    #> [22] cli_3.6.4           crayon_1.5.3        rlang_1.1.6
    #> [25] R.methodsS3_1.8.2   parallelly_1.43.0   munsell_0.5.1
    #> [28] withr_3.0.2         cachem_1.1.0        yaml_2.3.10
    #> [31] tools_4.5.0         parallel_4.5.0      colorspace_2.1-1
    #> [34] filelock_1.0.3      globals_0.16.3      assertthat_0.2.1
    #> [37] vctrs_0.6.5         R6_2.6.1            lifecycle_1.0.4
    #> [40] magick_2.8.6        stringr_1.5.1       furrr_0.3.1
    #> [43] pkgconfig_2.0.3     pillar_1.10.2       bslib_0.9.0
    #> [46] gtable_0.3.6        data.table_1.17.0   glue_1.8.0
    #> [49] Rcpp_1.0.14         xfun_0.52           tibble_3.2.1
    #> [52] tidyselect_1.2.1    knitr_1.50          farver_2.1.2
    #> [55] igraph_2.1.4        htmltools_0.5.8.1   rmarkdown_2.29
    #> [58] labeling_0.4.3      compiler_4.5.0