Demo dataset for: SPACEc, a streamlined, interactive Python workflow for multiplexed image processing and analysis

Description

Notes

Methods

Tissue samples:

Tonsil cores were extracted from a larger multi-tumor tissue microarray (TMA), which included a total of 66 unique tissues (51 malignant and semi-malignant tissues, as well as 15 non-malignant tissues). Representative tissue regions were annotated on corresponding hematoxylin and eosin (H&E)-stained sections by a board-certified surgical pathologist (S.Z.). Annotations were used to generate the 66 cores each with cores of 1mm diameter. FFPE tissue blocks were retrieved from the tissue archives of the Institute of Pathology, University Medical Center Mainz, Germany, and the Department of Dermatology, University Medical Center Mainz, Germany. The multi-tumor-TMA block was sectioned at 3µm thickness onto SuperFrost Plus microscopy slides before being processed for CODEX multiplex imaging as previously described.

CODEX multiplexed imaging and processing

To run the CODEX machine, the slide was taken from the storage buffer and placed in PBS for 10 minutes to equilibrate. After drying the PBS with a tissue, a flow cell was sealed onto the tissue slide. The assembled slide and flow cell were then placed in a PhenoCycler Buffer made from 10X PhenoCycler Buffer \& Additive for at least 10 minutes before starting the experiment. A 96-well reporter plate was prepared with each reporter corresponding to the correct barcoded antibody for each cycle, with up to 3 reporters per cycle per well. The fluorescence reporters were mixed with 1X PhenoCycler Buffer, Additive, nuclear-staining reagent, and assay reagent according to the manufacturer's instructions. With the reporter plate and assembled slide and flow cell placed into the CODEX machine, the automated multiplexed imaging experiment was initiated. Each imaging cycle included steps for reporter binding, imaging of three fluorescent channels, and reporter stripping to prepare for the next cycle and set of markers. This was repeated until all markers were imaged. After the experiment, a .qptiff image file containing individual antibody channels and the DAPI channel was obtained. Image stitching, drift compensation, deconvolution, and cycle concatenation are performed within the Akoya PhenoCycler software. The raw imaging data output (tiff, 377.442nm per pixel for 20x CODEX) is first examined with QuPath software (https://qupath.github.io/) for inspection of staining quality. Any markers that produce unexpected patterns or low signal-to-noise ratios should be excluded from the ensuing analysis. The qptiff files must be converted into tiff files for input into SPACEc. Data preprocessing includes image stitching, drift compensation, deconvolution, and cycle concatenation performed using the Akoya Phenocycler software. The raw imaging data (qptiff, 377.442 nm/pixel for 20x CODEX) files from the Akoya PhenoCycler technology were first examined with QuPath software (https://qupath.github.io/) to inspect staining qualities. Markers with untenable patterns or low signal-to-noise ratios were excluded from further analysis. A custom CODEX analysis pipeline was used to process all acquired CODEX data (scripts available upon request). The qptiff files were converted into tiff files for tissue detection (watershed algorithm) and cell segmentation.