Additional genomic data containers to combine
Each argument should be a genomic data object such as a SummarizedExperiment,
SingleCellExperiment, SpatialExperiment, or Seurat object (provided that
the appropriate method extensions are available). You may also provide a list
of such objects.
When row-binding, features (e.g., genes) are matched by name, and any missing
features will be filled with NA or zero as appropriate for the container.
When column-binding, samples (e.g., cells) are matched by position, so all objects
must have the same number of features. To match by value, not position, see mutate-joins.