Evidence map›Paper›PMID 39764138›Full record

ArticleResearch square2024

Identifying cell-type-specific spatially variable genes with ctSVG.

Haotian Zhuang, Xinyi Shang, Wenpin Hou, Zhicheng Ji

Abstract readPreprint
In one paragraph

Article in Research square, 2024. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Haotian ZhuangDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA.
Xinyi ShangDepartment of Biostatistics, Columbia University Mailman School of Public Health, New York City, NY, USA.
Wenpin HouDepartment of Biostatistics, Columbia University Mailman School of Public Health, New York City, NY, USA.
Zhicheng JiDepartment of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, NC, USA.

Funding

The Duke Senescent Cell Evaluations in Normal Tissues (SCENT) Mapping CenterU54AG075936 · NIA · DUKE UNIVERSITY · PI GLASS, CAROLYN · 2021 to 2025
$12.7M
Methods for inferring and analyzing gene regulatory networks using single-cell multiomics and spatial genomics dataR35GM150887 · NIGMS · DUKE UNIVERSITY · PI Wenpin Hou · 2023 to 2026
$1.6M
Computational methods for in situ spatial transcriptomicsR35GM154865 · NIGMS · DUKE UNIVERSITY · PI Zhicheng Ji · 2024 to 2026
$1.2M
Computational Methods for Inferring Single-cell DNA Methylation and its Spatial LandscapeR00HG011468 · NHGRI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HOU, WENPIN · 2022 to 2024
$747k
NHGRI NIH HHS R00 HG011468NIA NIH HHS U54 AG075936NIGMS NIH HHS R35 GM150887NIGMS NIH HHS R35 GM154865
6 · The paper itself

Abstract

Spatially variable genes (SVGs) reveal the molecular and functional heterogeneity of cells across different spatial regions of a tissue. We found that sample-wide SVGs, identified by previous methods across the whole sample, largely overlap with cell-type marker genes derived from single-cell gene expression, leaving the spatial location information largely underutilized. We developed ctSVG, a computational method specifically tailored for Visium HD spatial transcriptomics at single-cell resolution. ctSVG accurately assigns Visium squares to cells and identifies cell-type-specific SVGs. We show that cell-type-specific SVGs identified by ctSVG include many new genes that do not overlap with sample-wide SVGs or cell-type marker genes, and that these genes reveal important biological functions in real spatial datasets.

Identifiers

PMID39764138
PMCPMC11702777

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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.