CellBin:a generalist framework to process spatial omics data to cell level
This paper studied the problem of processing diverse spatial omics platforms to construct robust cell-level matrices, proposing a generalist computational framework called CellBin. CellBin unifies multi-field weighted image stitching, U-Net–based cell segmentation models trained across different staining modalities, and spot-to-cell mapping, using an optimized architecture for high-throughput processing. Across five technological platforms and three omics data types, CellBin reported consistently better performance than seven state-of-the-art methods in F1-score, cell size precision, and annotation accuracy, with the caveat that the paper evaluates robustness specifically across the included platform/omics set. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.
Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works
Abstract
Full text
1,228 characters
· extracted from
oa-doi-fallback
· click to expand
Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.
My notes (saved in your browser only)
Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works
Citation neighborhood (no data yet)
We don't have any in-corpus citations linked to this paper yet. This is a recent paper (2025) — citers typically take a year or two to land, and the OpenAlex reference graph may still be filling in.
Source provenance
- europepmc
- last seen: 2026-05-20T01:45:00.602351+00:00