Evidence map›Paper›PMID 39229093›Full record

ArticlebioRxiv : the preprint server for biology2024

SPACE: Spatially variable gene clustering adjusting for cell type effect for improved spatial domain detection.

Sikta Das Adhikari, Nina G Steele, Brian Theisen, Jianrong Wang, Yuehua Cui

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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

5 authors.

Sikta Das AdhikariDepartment of Computational Mathematics, Science and Engineering, Michigan State University, East Lansing, MI.ORCID 0009-0006-2433-8200
Nina G SteeleDepartment of Surgery, Henry Ford Pancreatic Cancer Center, Henry Ford Hospital, Detroit, MI.ORCID 0000-0003-1564-3562
Brian TheisenDepartment of Pathology, Henry Ford Health, Detroit, MI.ORCID 0009-0004-1079-8594
Jianrong WangDepartment of Computational Mathematics, Science and Engineering, Michigan State University, East Lansing, MI.ORCID 0000-0002-9290-4888
Yuehua CuiDepartment of Statistics and Probability, Michigan State University, East Lansing, MI, 48824, USA.ORCID 0000-0001-8099-1753

Funding

Statistical modeling of long-range chromatin interactions on gene regulation and underlying molecularR01GM131398 · NIGMS · MICHIGAN STATE UNIVERSITY · PI WANG, JIANRONG · 2018 to 2021
$1.3M
Investigating Cellular Communication in the Tumor Microenvironment in Pancreatic CancerR00CA263154 · NCI · HENRY FORD HEALTH SYSTEM · PI STEELE, NINA G · 2022 to 2024
$862k
NCI NIH HHS R00 CA263154NIGMS NIH HHS R01 GM131398
6 · The paper itself

Abstract

Recent advances in spatial transcriptomics have significantly deepened our understanding of biology. A primary focus has been identifying spatially variable genes (SVGs) which are crucial for downstream tasks like spatial domain detection. Traditional methods often use all or a set number of top SVGs for this purpose. However, in diverse datasets with many SVGs, this approach may not ensure accurate results. Instead, grouping SVGs by expression patterns and using all SVG groups in downstream analysis can improve accuracy. Furthermore, classifying SVGs in this manner is akin to identifying cell type marker genes, offering valuable biological insights. The challenge lies in accurately categorizing SVGs into relevant clusters, aggravated by the absence of prior knowledge regarding the number and spectrum of spatial gene patterns. Addressing this challenge, we propose SPACE, SPatially variable gene clustering Adjusting for Cell type Effect, a framework that classifies SVGs based on their spatial patterns by adjusting for confounding effects caused by shared cell types, to improve spatial domain detection. This method does not require prior knowledge of gene cluster numbers, spatial patterns, or cell type information. Our comprehensive simulations and real data analyses demonstrate that SPACE is an efficient and promising tool for spatial transcriptomics analysis.

Indexed as

Gene spatial pattern classificationSpatial domainSpatially variable genesSpatial Transcriptomics

Identifiers

PMID39229093
PMCPMC11370608

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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.