singIST: an R/Bioconductor library and Quarto dashboard for automated single-cell comparative transcriptomics analysis of disease models and humans

preprint OA: closed
Full text JSON View at publisher
AI-generated deep summary by claude@2026-06, 2026-06-24 · read from full text

This paper introduces singIST, an R/Bioconductor library and Quarto/Shiny dashboard for automated, quantitative, explainable comparisons of disease-model scRNA-seq data to a human reference by mapping one-to-one orthologs and cell types and translating learned model fold changes into the human expression space. The method uses an adaptive sparse multi-block PLS-DA model fitted on human pseudobulk expression to compute signed recapitulation at superpathway, cell type, and gene levels, with an emphasis on streamlined interpretation and exportable outputs via the companion Visualizer. As a demonstrated workflow, the authors apply singIST to an oxazolone mouse model compared with a human atopic dermatitis reference for two example pathways. The paper explicitly frames translation challenges due to preclinical–human divergence, but does not provide additional benchmarking beyond the illustrated workflow. 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

Full text 1,522 characters · extracted from oa-doi-fallback · click to expand
Abstract Preclinical disease models often diverge from human pathophysiology at single-cell resolution, complicating model selection and limiting translational value. We present singIST, an R/Bioconductor package for quantitative and explainable comparison of disease model scRNA-seq data against a human reference. For each superpathway, singIST fits an adaptive sparse multi-block PLS-DA model on human pseudobulk expression, integrated one-to-one orthology and cell type mapping, and translates model fold changes into the human expression space to compute signed recapitulation at the superpathway, cell type, and gene levels. To streamline interpretation and reporting, we provide singIST Visualizer, a companion Quarto/Shiny dashboard that loads singIST outputs and offers interactive exploration with export ready plots and tables, avoiding manual figure coding across many superpathways and models. We demonstrate the workflow. We illustrate an end-to-end workflow on an oxazolone mouse model against a human atopic dermatitis reference for two representative pathways: Dendritic Cells in regulating Th1/Th2 Development [BIOCARTA] and Cytokine-cytokine receptor interaction [KEGG]. singIST is distributed under the MIT License via Bioconductor, and the Visualizer is available on GitHub. Competing Interest Statement I have read the journal's policy and the authors of this manuscript have the following competing interests: AM, SP and FF, are all paid employees of Almirall S.A and may hold shares in the company.

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)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

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 (2026) — 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