initiateSpataObjectVisiumHD: Initiate an object of class 'SPATA2' from platform VisiumHD

In theMILOlab/SPATA2: A Toolbox for Spatial Expression Analysis

Initiate an object of class SPATA2 from platform VisiumHD

Description

This function initiates a SPATA2 object with data generated using the 10x Genomics VisiumHD platform.

Usage

initiateSpataObjectVisiumHD(
  sample_name,
  directory_visium,
  square_res = "16um",
  mtr = "filtered",
  genes = NULL,
  workers = 1,
  batch_size = 1000,
  img_active = "lowres",
  img_ref = "hires",
  resize_images = NULL,
  unload = TRUE,
  verbose = TRUE
)

Arguments

sample_name	Character. The name of the sample.
directory_visium	Character. The directory containing the Visium output files.
square_res	Character. The square resolution from which to load the data. While c('16um', '8um', '2um') are the default resolutions, reduceResolutionVisiumHD() is applied if the input deviates from these three input options. See section Visium HD Resolution for more information.
mtr	Character. Specifies which matrix to use, either "filtered" or "raw". Default is "filtered".
genes	Character or NULL. If character, specifies beforehand which genes to keep in the count matrix. If NULL, the default, all genes are kept.
workers	Integer specifying the number of parallel workers to use for processing. Default is 1, which defaults to no parallel workers. If 2 or more, the furrr package is required.
batch_size	Integer specifying the number of spatial spots to process in each batch. Default is 1000.
img_active	Character. The active image to use, either "lowres" or "hires". Default is "lowres".
img_ref	Character. The reference image to use, either "lowres" or "hires". Default is "hires".
resize_images	A named list of numeric values between 0-1 used to resize the respective image as indicated by the slot name. E.g resize_images = list(hires = 0.5) resizes the hires image to 50% of its original scale.
unload	Logical value. If TRUE, every image except for the active image is unloaded.
verbose	Logical. If TRUE, informative messages regarding the computational progress will be printed. (Warning messages will always be printed.)

Details

The function requires a directory containing the output files from a 10x Genomics VisiumHD experiment specified with the argument directory_visium. This directory (below denoted as ~) must include the following sub-directories:

• ~/binned_outputs: A folder with the following subdirectories.

  • ~/binned_outputs/square_002um: The folder containing the data for square_res = '2um'.

  • ~/binned_outputs/square_008um: The folder containing the data for square_res = '8um'.

  • ~/binned_outputs/square_016um: The folder containing the data for square_res = '16um'.

Depending on your input for square_res only the corresponding subfolder is required. This subfolder should contain the following files and sub-directories:

• ~/binned_outputs/<square_res>/filtered_feature_bc_matrix.h5 or ~/raw_feature_bc_matrix.h5: The HDF5 file containing the filtered or raw feature-barcode matrix, respectively.

• ~/binned_outputs/<square_res>/spatial/tissue_lowres_image.png or ~/spatial/tissue_hires_image.png: The low-resolution or high-resolution tissue image.

• ~/binned_outputs/<square_res>/spatial/scalefactors_json.json: A JSON file containing the scale factors for the images.

• ~/binned_outputs/<square_res>/spatial/tissue_position.parquet A .parguet file containing the tissue positions and spatial coordinates.

The function will check for these files and process them to create a SPATA2 object. It reads the count matrix, loads the spatial data, and initializes the SPATA2 object with the necessary metadata and settings.

Value

A SPATA2 object the VisiumHD platform.

Visium HD Resolution

The input for square_res can deviate from the standard resolution options as long as it is an even number divisible by one of the standard resolutions. In such cases, data from the next possible lower resolution is read, and reduceResolutionVisiumHD() is applied to aggregate the data. For example, if square_res = '6um', data is retrieved from ~/binned_outputs/square_002um and then aggregated accordingly. The same applies if ⁠square_res = 10um⁠. If ⁠square_res = 24um⁠, data is read from ~/binned_outputs/square_008um; if ⁠square_res = 32um⁠, data is read from ~/binned_outputs/square_016um, and so on. If the required folder is missing, data from the next higher resolution folder is used if possible, else an error is thrown.

Note, that aggregating counts by resolution can take a considerable amount of time. Consider prefiltering the raw counts using genes and/or increasing the number of cores to use with workers.

Row and column indices

Visium spot coordinates come with column and row indices. The functions initiateSpataObjectVisium() and initiateSpataObjectVisiumHD() ensure that col aligns with the direction of the x-coordinates and that row aligns with the direction of the y-coordinates. If they do not, they are adjusted accordingly. Hence, these variables should not be used as keys for data merging.

Note

It is crucial to install the package arrow in a way that arrow::read_parquet() works. There are several ways. Installing the package with install.packages('arrow', repos = 'https://apache.r-universe.dev') worked reliably for us.

theMILOlab/SPATA2 documentation built on Feb. 8, 2025, 11:41 p.m.