Evidence map›Paper›PMID 38902953›Full record

ArticleBioinformatics (Oxford, England)2024

SEraster: a rasterization preprocessing framework for scalable spatial omics data analysis.

Gohta Aihara, Kalen Clifton, Mayling Chen, Zhuoyan Li, Lyla Atta, Brendan F Miller, Rahul Satija, John W Hickey, Jean Fan

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  8. SpotSweeper: spatially-aware quality control for spatial transcriptomics.bioRxiv : the preprint server for biology · 2024
    Article
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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

9 authors.

Gohta AiharaCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21211, United States.
Kalen CliftonCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21211, United States.
Mayling ChenCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21211, United States.
Zhuoyan LiNew York Genome Center, New York, NY 10013, United States.
Lyla AttaCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21211, United States.
Brendan F MillerCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21211, United States.
Rahul SatijaNew York Genome Center, New York, NY 10013, United States.
John W HickeyDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, United States.
Jean FanCenter for Computational Biology, Whiting School of Engineering, Johns Hopkins University, Baltimore, MD 21211, United States.ORCID 0000-0002-0212-5451

Funding

Center for Integrated Cellular Analysis - Valeria A. Sanchez EstradaRM1HG011014 · NHGRI · NEW YORK GENOME CENTER · PI LANDAU, DAN, SATIJA, RAHUL · 2020 to 2025
$22.1M
The Duke Senescent Cell Evaluations in Normal Tissues (SCENT) Mapping CenterU54AG075936 · NIA · DUKE UNIVERSITY · PI GLASS, CAROLYN · 2021 to 2025
$12.7M
Comprehensive reference atlas construction, geolocation and data integration for HuBMAP HIVE [5 of 5]OT2OD033760 · OD · NEW YORK GENOME CENTER · PI SATIJA, RAHUL · 2022 to 2025
$6.1M
National Science Foundation 2047611NHGRI NIH HHS RM1 HG011014NIA NIH HHS U54 AG075936NIH HHS OT2 OD033760
6 · The paper itself

Abstract

motivationSpatial omics data demand computational analysis but many analysis tools have computational resource requirements that increase with the number of cells analyzed. This presents scalability challenges as researchers use spatial omics technologies to profile millions of cells.

resultsTo enhance the scalability of spatial omics data analysis, we developed a rasterization preprocessing framework called SEraster that aggregates cellular information into spatial pixels. We apply SEraster to both real and simulated spatial omics data prior to spatial variable gene expression analysis to demonstrate that such preprocessing can reduce computational resource requirements while maintaining high performance, including as compared to other down-sampling approaches. We further integrate SEraster with existing analysis tools to characterize cell-type spatial co-enrichment across length scales. Finally, we apply SEraster to enable analysis of a mouse pup spatial omics dataset with over a million cells to identify tissue-level and cell-type-specific spatially variable genes as well as spatially co-enriched cell types that recapitulate expected organ structures. AVAILABILITY AND IMPLEMENTATION: SEraster is implemented as an R package on GitHub (https://github.com/JEFworks-Lab/SEraster) with additional tutorials at https://JEF.works/SEraster.

Indexed as

SoftwareAlgorithmsAnimalsComputational BiologyGene Expression ProfilingMice

Identifiers

PMID38902953
PMCPMC11226864

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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 OpenQuestion graph.