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Technology-invariant pipeline for spatial omics analysis (Xenium / MERSCOPE / CosMx / PhenoCycler / MACSima / Hyperion) that scales to millions of cells

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I trained a cellpose model and used it with a morphology2D file outside of sopa and got pretty good results, however when running it with the same image on sopa...

Hi Sopa development team, Sopa looks like a perfect fit for what I've been trying to do with integrating IF stains with Baysor re-segmentation. However, I've been having trouble figuring...

Thanks for the software, it's a very comprehensive effort. We just got some CosMX data and are pretty unhappy with the default segmentations. We were on the way of training...

Hello to the SOPA creators. I am quite a beginner to Python and the Command Line Interface. I have attempted to run the Ready made Snakemake pipeline for Xenium data...

Hi, Thank you for SOPA, it looks really helpful. I'd love to use the cell segmentation resolver. However, I'm struggling a little with how best to implement. I have custom...

**Is your feature request related to a problem? Please describe.** I think the output of CosMX files has changed since sopa was developed. **Describe the solution you'd like** Could you...

The `snakemake` pipeline should be translated to `nextflow` to reach more users. Don't hesitate to comment this issue to show your interest, else we keep it as a low priority...

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help wanted

**Feature request** I am using multiplexed images (Opal dyes - fluorescence data) acquired with a Zeiss microscope that generates **.czi** files, but this format is not compatible with SOPA. **Suggested...

**Feature request / question** In the absence of a general membrane marker, Sopa/cellpose (using only DAPI) will not "expand" the detected nuclei to generate an artificial cell membrane/cytoplasm area. In...

snakemake --config sdata_path=tuto.zarr --configfile=config/toy/uniform_cellpose.yaml --cores 1 --use-conda i did not find the tuto.zarr in the workflow or anywhere in the snakemake folder