Modern biological experiments are increasingly producing interesting matrices. These may represent the presence or absence of specific gene mutations, copy number variants, microRNAs, or other molecular or clinical phenomena. We have recently developed a tool, *CytoGPS* [^Abrams and colleagues], that converts conventional karyotypes from the standard text-based notation (the International Standard for Human Cytogenetic Nomenclature; ISCN) into a binary vector with three bits (loss, gain, or fusion) per cytoband, which we call the “LGF model”.

The `Mercator` package is intended to facilitate the exploration of data sets. It implements metrics for continuous, categorical, and binary data, including a subset of the 76 binary distance metrics described by [^Choi and colleagues], ensuring that at least one representative of each of their major clusters is included. Each resulting distance matrix can be combined with multiple visualization techniques, providing a consistent interface to thoroughly explore the data set.

In this vignette, we focus initially on the tools for dealing with binary matrices. We start by loading the package.

We proceed with a model dataset of karyotypes from patients with Chronic Myelogenous Leukemia (CML) with 400 chromosomal features recorded over 740 patients, from the public Mitelman database. Cytogenetic abnormalities recorded in Mitelman as text strings have been pre-processed with CytoGPS into binary vectors. For the sake of clarity and efficiency we have chosen a subset of patients and features for this example.

```
filename <- system.file("Examples/Mercator_Test_Data.csv", package="Mercator")
my.data <- read.csv(filename, header=TRUE)
dim(my.data)
```

`## [1] 740 400`

Many of the functions of the `Mercator` package operate on a `BinaryMatrix` S4 object, which serves as an input to subsequent functions and visualizations.

A `BinaryMatrix` object is formed from a matrix containing integer or numeric values. Although `Mercator` was intially designed for processing and visualizing binary data, the `BinaryMatrix` object and subsequent functions accept a variety of integer and numeric values. In addition, all the visualization tools work with an arbitrary distance matrix; see the vignette Mercator for Continuous Data.

Row and column names, along with optional annotations, can be assigned as for data frames. If no row or column headings are assigned, the `BinaryMatrix` takes the row and column names of the input matrix by default. Notice that the resulting object always includes a “history” element that tracks how it has been processed.

```
## An object of the 'BinaryMatrix' class, of size
## [1] 740 400
## History:
## [1] "Newly created."
```

We wish to cluster the whole karyotypes of each patient to identify the patterns of important chromosomal abnormalities that link them. To proceed, we must transpose the `BinaryMatrix`. Transposition meaningfully transposes the row and column headings of the `BinaryMatrix`, as well.

```
## An object of the 'BinaryMatrix' class, of size
## [1] 400 740
## History:
## [1] "Newly created." "transposed"
```

The binary feature-vectors (viewed across a population of patient samples) are rarely unique. Having identical feature vectors can complicate some of the clustering and visualization routines that we want to use (often by introducing a division by zero). However, they can also alter the biological implications by automatically giving more “weight” to a single genomic event (like a trisomy or monosomy). To deal with this issue, the `Mercator` package includes a function to remove duplicate or redundant features.

```
## An object of the 'BinaryMatrix' class, of size
## [1] 400 136
## History:
## [1] "Newly created." "transposed"
## [3] "Duplicate features removed."
```

In the case of our data, only 136 of the 740 karyotypes are unique. Some of the karyotypes are “not used” in the sense that they contain none of the abnormalities selected for this limited subset.

`## [1] 65`

`## [1] "R17" "R18" "R23" "R34" "R44" "R51"`

By contrast, many features are *used* but are simply redundant.

`## [1] 539`

`Mercator` provides easy access to functions of the `Thresher` R package, which includes outlier detection and estimates of the number of clusters [^Wang and colleagues]. The underlying idea is that the features can be viewed as “weight vectors” in a principal component space trying to display the samples. The lengths of the vectors are a measure of their importance in the data set; short vectors can (and probably should) be removed since they do not carry much useful information. We have incorporated that feature into the `Mercator` package.

We create a `ThreshedBinaryMatrix` to implement the algorithm. Based on simulations described in the Thresher paper, a cutoff above approximately 0.3 can be used to select informative features. Then, we subset our `ThreshedBinaryMatrix` to only include features above our given cutoff.

```
## An object of the 'BinaryMatrix' class, of size
## [1] 400 111
## History:
## [1] "Newly created." "transposed"
## [3] "Duplicate features removed." "Threshed."
```

The red vertical line in the figure indicates the cutoff we have chosen to separate uninformative features (<0.3) from informative ones (>0.3).

```
Delta <- my.binmat@thresher@delta
hist(Delta, breaks=20, main="", xlab="Weight", col="gray")
abline(v=0.3, col='red')
```

The `ThreshedBinaryMatrix` object contains a `reaper` slot that estimates the number of principal components and the number of clusters after outliers have been removed. These values can be viewed numerically…

`## [1] 2`

`## [1] 5`

… or they can be visualized with an *Auer-Gervini plot* (where we are looking for a “long step”) …

```
plot(my.binmat@reaper@ag, ylim=c(0, 30))
abline(h=my.binmat@reaper@pcdim, col="forestgreen", lwd=2)
abline(h=7, col="orange", lwd=2)
```

```
pts <- screeplot(my.binmat@reaper, xlim=c(0,30))
abline(v=pts[my.binmat@reaper@pcdim], col="forestgreen", lwd=2)
abline(v=pts[7], col="orange", lwd=2)
```

There is no method that can definitely identify the number of clusters for a “perfect” solution, leaving part of the decision to the analyst’s judgment. Auer-Gervini and Scree plots provide informative visualizations to facilitate this interference. The default value provided by the Auer-Gervini analysis (N=2; green) is somewhat conservative. The value provided by the broken-stick model (N=7; orange) overlaid on the scree plot is more aggressive, but is not too unreasonable based on the Auer-Gervini plot. While one could make the argument that the correct number of groups is at least seven, we will begin by using the number of groups recommended by Thresher.

The `Mercator` package allows visualization of data with methods that include both standard techniques (hierarchical clustering) and large-scale visualizations (multidimensional scaling (MDS), t-distributed Stochastic Neighbor Embedding (t-SNE), and iGraph.)

The `Mercator` package implements or provides access to 10 distance metrics: Jaccard, Sokal-Michener, Hamming, Russell-Rao, Pearson, Goodman-Kruskal, Manhattan, Canberra, Binary, and Euclidean. Although some of these metrics can be used for continuous or categorical data, all are appropriate for binary matrices. `Mercator` allows the user to compare different metrics and select one that is useful for a given dataset.

Here, we will use the Jaccard distance because of its ease of interpretability, common usage, and its appropriatness of application to asymmetric binary data, such as the binary vector output of CytoGPS in this dataset. The `Mercator` constructor can be called with any initial visualization, and visualizations can be added in an arbitrary order.

We can represent all the distances between features within the dissimilarity matrix we have calculated on our data as a histogram, as a visual representation of relatedness.

Mercator allows us to implement common, standard visualizations such as hierarchical clustering…

In this dendrogram, there appear to be at least three different “blue” branches, suggesting that there are more than the conservative estimate of five clusters obtained from `Thresher`. We will take a look at the data using another visualization technique before making a final decision.

`Mercator` can use t-distributed Stochastic Neighbor Embedding (t-SNE) plots for visualizing large-scale, high-dimensional data in 2-dimensional space.

```
jacc.Vis <- addVisualization(jacc.Vis, "tsne", perplexity=25)
plot(jacc.Vis, view = "tsne", main="t-SNE; Jaccard Distance")
```

Optional t-SNE parameters, such as perplexity, can be used to fine-tune the plot as the visualization is created. Using `addVisualization` to create a new, tuned plot of an existing type overwrites the existing plot of that type.

```
## Warning in addVisualization(jacc.Vis, "tsne", perplexity = 10): Overwriting an
## existing visualization:tsne
```

It does not appear that a smaller perplexity is useful for this data set.

`Mercator` allows visualization of multi-dimensional scaling (MDS) plots, as well.

```
jacc.Vis <- addVisualization(jacc.Vis, "mds")
plot(jacc.Vis, view = "mds", main="MDS; Jaccard Distance")
```

At this point, we still don’t know if we should increase the number of clusters in the data set form 5 to 7. Fortunately, we have access to the “silhouette width”, which measures how well each element in the data set appears to be clustered.

Ths plot of the silhouette widths confirms our suspicion from the hierarchical clustering dendrogram that the “blue” group is not as coherent/consistent as the other grousp. So, we are going to try reclustering to label more clusters.

There is some improvement when K=6, but a clearly worse result when K = 7. For the rest of our analysis, we will switch to ooking at 6 groups.

`Mercator` can be used to visualize complex networks using iGraph. To improve clarity of the visualization and computational time, we have implement the `downsample` function to reduce the number of data points to be linked and visualized. The idea goes back to Peng Qiu’s implementation of the SPADE clustering algorithm for mass cytometry data. The main point is to *under* sample the densest regions of the data space to make it more likely that rarer clusters will still be adequately sampled. (While not required with the current data set, this idea can be quite useful with data sets containing tens of thousands of objects.)

**Note:** The `Mercator` class includes a “subset” operator that tries to preserve earlier visualizations. This operator is fast for MDS or t-SNE models, but is very slow for large hierarchical clustering. (It uses the implementation in the `dendextend` package, which works by removing a single leaf at a time from the tree.) In the next code chunk, we `downsample` to create a meaningful subset, and then compute a new dendrogram for each subset.

```
X <- jacc.Vis
X@view[["hclust"]] <- NULL # remove this view
N <- as.matrix(X@distance)
set.seed(87530)
P <- downsample(40, N, 0.1) # create a downsampled subset
J <- X[P]
names(J@view) # need to compute a new dendrogram
```

`## [1] "tsne" "mds"`

`## [1] "tsne" "mds" "hclust"`

Because our data set is small enough, we are going to create our graphical views from the oriinal object rather than the downsampled one. We can look at the resulting graph using three different “layouts”.

```
jacc.Vis <- addVisualization(jacc.Vis, "graph", Q =0.5)
plot(jacc.Vis, view = "graph", layout = "tsne", main="T-SNE Layout")
```

We can use the *getClusters* function to characterize each cluster and use these for further manipulation.

We can easily determine cluster size…

```
## my.clust
## 1 2 3 4 5 6
## 55 24 7 11 7 7
```

… or the patients that comprise each cluster.

```
## [1] "R62" "R68" "R72" "R108" "R333" "R412" "R436" "R502" "R503" "R679"
## [11] "R705"
```

Finally, we are going to look at what happens if we use a different distance metric.

```
set.seed(8642)
sokal.Vis <- Mercator(my.binmat, "sokal", "tsne", K=kk, peplexity = 10)
table(getClusters(sokal.Vis), getClusters(jacc.Vis))
```

```
##
## 1 2 3 4 5 6
## 1 55 0 7 11 3 3
## 2 0 16 0 0 0 0
## 3 0 8 0 0 0 0
## 4 0 0 0 0 4 0
## 5 0 0 0 0 0 2
## 6 0 0 0 0 0 2
```

The two largest groups get assigned the same colors (by chance) in the Jaccard and the Sokal-Michener clusterings. However, it is not at all clear how to align the smaller groups. For that purpose we can use the `remapColors` function.

```
##
## 1 2 3 4 5 6
## 1 55 0 7 11 3 3
## 2 0 16 0 0 0 0
## 3 0 8 0 0 0 0
## 4 0 0 0 0 0 2
## 5 0 0 0 0 4 0
## 6 0 0 0 0 0 2
```

Now colors have been matched (as well as possible) between the two sets of visualizations.

Each `Mercator`

object stores its own palette internally, but you can change the palette using the `slot`

funciton.

```
slot(jacc.Vis, "palette") <- c("red", "orange", "green", "blue",
"cyan", "magenta", "purple", "black")
plot(jacc.Vis, view = "tsne")
```

If the number of colors in the palette is smaller than the number of clusters, they will be recycled, and other plotting symbols will be introduced.

[^Abrams and colleagues]: Abrams ZB, Zhang L, Abruzzo LV, Heerema NA, Li S, Dillon T, Rodriguez R, Coombes KR, Payne PRO. CytoGPS: A Web-Enabled Karyotype Analysis Tool for Cytogenetics. Bioinformatics. 2019 Jul 2. doi: 10.1093/bioinformatics/btz520. (Epub ahead of print)

[^Choi and colleagues]: Choi SS, Cha SH, Tappert CC. A Survey of Binary Similarity and Distance Measures. Systemics, Cybernetics, and Informatics 2010;8(1):43-48.

[^Wang and colleagues]: Wang M, Abrams ZB, Kornblau SM, Coombes KR. Thresher: determining the number of clusters while removing outliers. BMC Bioinformatics 2018;19(1):9.