Evidence map›Paper›PMID 41719583›Full record

ArticleDatabase : the journal of biological databases and curation2026

huSA: a comprehensive database for multi-dimensional resolution of bulk, single cell and spatial transcription profiles in skin diseases.

Meiling Zheng, Bao Qian, Zhi Hu, Xingyu Wei, Ke Sun, Wenjuan Jiang, Changxing Gao, Ming Zhao

Abstract read
In one paragraph

Article in Database : the journal of biological databases and curation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Meiling ZhengHospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, 210042, China.
Bao QianHospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, 210042, China.
Zhi HuHospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, 210042, China.
Xingyu WeiHospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, 210042, China.
Ke SunHospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, 210042, China.
Wenjuan JiangHospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, 210042, China.
Changxing GaoHospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, 210042, China.
Ming ZhaoHospital for Skin Diseases, Institute of Dermatology, Chinese Academy of Medical Sciences & Peking Union Medical College, Nanjing, 210042, China.ORCID 0000-0002-1320-1093

Funding

Chinese Academy of Medical Sciences 2022-RC310-04National Key Research and Development Program of China 2022YFC3601803National Natural Science Foundation of China 82030097National Natural Science Foundation of China 82404153National Natural Science Foundation of China 82473535
6 · The paper itself

Abstract

backgroundSkin diseases are among the most prevalent conditions worldwide, posing significant threats to human health by causing physical discomfort, psychological distress, and reduced quality of life. With the rapid advancement of high-throughput technologies, a substantial number of transcriptomic datasets, including single-cell RNA sequencing (scRNA-seq), spatial transcriptomics, and bulk RNA-seq, have been generated in the field of dermatology over the past decade. However, the lack of effective integration and standardized analysis pipelines limits the full utilization of these valuable resources in skin disease research.

objectivesTo address this gap, we aimed to construct a comprehensive, integrative, and user-friendly atlas that enables systematic exploration of skin transcriptomic data across multiple diseases and modalities.

methodsWe developed the Human Skin Atlas (huSA) ('https://humanskinatlas.com/index.html'), a publicly accessible database that incorporates data from 17 skin diseases and 63 independent datasets, including 1 434 scRNA-seq, 63 spatial transcriptomics, and 1 502 bulk RNA-seq samples. The database provides standardized cell-type annotations, differential gene expression analysis, cell-cell interaction mapping, pathway and metabolic module enrichment, transcription factor regulatory inference, and differentiation state assessment for scRNA-seq data. Data from identical skin diseases were further integrated to enhance biological signal detection. For visualization, we embedded the 'cell × gene' and 'Cirrocumulus' platforms, offering interactive and customizable gene expression visualizations at both single-cell and spatial levels with user-defined parameters.

resultsThe huSA enables both individual dataset analysis and cross-dataset integration, providing robust, consistent, and scalable insights into skin disease biology. Demonstration analyses confirmed that results derived from either single datasets or aggregated multi-dataset integrations exhibited high reliability and biological relevance. The platform successfully supports diverse research needs, including cell-type-specific expression profiling, regulatory network construction, and spatial transcriptomic exploration.

conclusionsThe Human Skin Atlas (huSA) represents a state-of-the-art integrative resource for the skin research community. By offering multiscale analyses and interactive visualization tools, the huSA accelerates the discovery of molecular mechanisms underlying skin diseases and facilitates translational research efforts aimed at improving skin health.

Indexed as

Databases, GeneticGene Expression ProfilingSingle-Cell AnalysisSkin DiseasesTranscriptomeBiocurationHumansSingle-Cell Gene Expression AnalysisSpatial Transcriptomics

Identifiers

PMID41719583
PMCPMC12923168

What Socratic holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.