Evidence map›Paper›PMID 39974940›Full record

ArticlebioRxiv : the preprint server for biology2025

scBSP: A fast and accurate tool for identifying spatially variable features from high-resolution spatial omics data.

Jinpu Li, Mauminah Raina, Yiqing Wang, Chunhui Xu, Li Su, Qi Guo, Ricardo Melo Ferreira, Michael T Eadon, Qin Ma, Juexin Wang and 1 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

Jinpu LiInstitute for Data Science and Informatics, University of Missouri, Columbia, MO 65211, USA.
Mauminah RainaDepartment of Biomedical Engineering and Informatics, Indiana University Indianapolis, Indianapolis, IN 46202, USA.
Yiqing WangChristopher S. Bond Life Sciences Center, University of Missouri, Columbia, MO 65211, USA.
Chunhui XuInstitute for Data Science and Informatics, University of Missouri, Columbia, MO 65211, USA.
Li SuInstitute for Data Science and Informatics, University of Missouri, Columbia, MO 65211, USA.
Qi GuoDepartment of Biomedical Informatics, College of Medicine, The Ohio State University, Columbus, OH 43210, USA.
Ricardo Melo FerreiraDepartment of Medicine, Indiana University Indianapolis, Indianapolis, IN 46202, USA.
Michael T EadonDepartment of Medicine, Indiana University Indianapolis, Indianapolis, IN 46202, USA.
Qin MaDepartment of Biomedical Informatics, College of Medicine, The Ohio State University, Columbus, OH 43210, USA.
Juexin WangDepartment of Biomedical Engineering and Informatics, Indiana University Indianapolis, Indianapolis, IN 46202, USA.ORCID 0000-0002-2260-4310
Dong XuInstitute for Data Science and Informatics, University of Missouri, Columbia, MO 65211, USA.ORCID 0000-0002-4809-0514

Funding

TriState SenNET (Lung and Heart) Tissue Map and Atlas consortiumU54AG075931 · NIA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TOREN FINKEL, Melanie Koenigshoff · 2021 to 2026
$14.0M
Multi-view self-supervised deep learning for biological sequences and beyondR35GM126985 · NIGMS · UNIVERSITY OF SOUTH FLORIDA · PI DONG XU · 2018 to 2026
$3.8M
Statistical Power Analysis Framework for Multi-Sample and Cross-Platform Spatial Omics ExperimentsR01GM152585 · NIGMS · OHIO STATE UNIVERSITY · PI Dongjun Chung, Qin Ma · 2024 to 2026
$1.2M
SCH: Graph-based Spatial Transcriptomics Computational Methods in Kidney DiseasesR01DK138504 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Michael Thomas Eadon, Qin Ma · 2023 to 2026
$1.1M
Statistical Power Calculation Framework for Spatially Resolved Transcriptomics ExperimentsR21HG012482 · NHGRI · OHIO STATE UNIVERSITY · PI CHUNG, DONGJUN, MA, QIN · 2022 to 2023
$421k
NHGRI NIH HHS R21 HG012482NIA NIH HHS U54 AG075931NIDDK NIH HHS R01 DK138504NIGMS NIH HHS R01 GM152585NIGMS NIH HHS R35 GM126985
6 · The paper itself

Abstract

Emerging spatial omics technologies empower comprehensive exploration of biological systems from multi-omics perspectives in their native tissue location in two and three-dimensional space. However, sparse sequencing capacity and growing spatial resolution in spatial omics present significant computational challenges in identifying biologically meaningful molecules that exhibit variable spatial distributions across different omics. We introduce scBSP, an open-source, versatile, and user-friendly package for identifying spatially variable features in high-resolution spatial omics data. scBSP leverages sparse matrix operation to significantly increase computational efficiency in both computational time and memory usage. In diverse spatial sequencing data and simulations, scBSP consistently and rapidly identifies spatially variable genes and spatially variable peaks across various sequencing techniques and spatial resolutions, handling two- and three-dimensional data with up to millions of cells. It can process high-definition spatial transcriptomics data for 19,950 genes across 181,367 spots within 10 seconds on a typical desktop computer, making it the fastest tool available for handling such high-resolution, sparse spatial omics data while maintaining high accuracy. In a case study of kidney disease using 10x Xenium data, scBSP identified spatially variable genes representative of critical pathological mechanisms associated with histology.

Identifiers

PMID39974940
PMCPMC11838397

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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 OpenQuestion graph.