Evidence map›Paper›PMID 34154649›Full record

ArticleGenome biology2021

SPARK-X: non-parametric modeling enables scalable and robust detection of spatial expression patterns for large spatial transcriptomic studies.

Jiaqiang Zhu, Shiquan Sun, Xiang Zhou

Abstract read
In one paragraph

Article in Genome biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 179 papers.

0numbers the graph read from it
0cells of the map it votes in
179citing 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

179 citing papers in PubMed.

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119 more citing papers are in PubMed but not listed here.

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

3 authors.

Jiaqiang ZhuDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, 48109, USA.
Shiquan SunDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, 48109, USA.
Xiang ZhouDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, 48109, USA. xzhousph@umich.edu.ORCID 0000-0002-4331-7599

Funding

Quantitative definition of cell identity from single-cell multi-omic, spatial, and perturbation dataR01HG010883 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Joshua Welch · 2019 to 2026
$4.4M
Statistical Methods for Modeling Polygenic Architecture in Association and Re-sequencing StudiesR01HG009124 · NHGRI · YALE UNIVERSITY · PI Xiang Zhou · 2017 to 2026
$3.0M
New directions in single cell genomics method developmentR01GM126553 · NIGMS · UNIVERSITY OF CHICAGO · PI Mengjie Chen · 2017 to 2026
$2.9M
Early adversity and DNA methylation in a primate model of stress and development.R01HD088558 · NICHD · DUKE UNIVERSITY · PI TUNG, JENNY · 2017 to 2021
$2.0M
Develop new bioinformatics infrastructures and computational tools for epitranscriptomics dataR01HG012927 · NHGRI · UNIVERSITY OF CHICAGO · PI Mengjie Chen · 2023 to 2026
$1.6M
Developing new computational tools for spatial transcriptomics dataR01HG011883 · NHGRI · UNIVERSITY OF CHICAGO · PI CHEN, MENGJIE, ZHOU, XIANG · 2021 to 2024
$1.5M
DMS/NIGMS 2: Advanced Statistical Methods for Spatially Resolved Transcriptomics StudiesR01GM144960 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ZHOU, XIANG · 2021 to 2024
$1.3M
Molecular interactions of mammalian circadian clock proteinsR01GM104496 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI TAKAHASHI, JOSEPH S, ZHANG, HONG · 2013 to 2016
$1.2M
NHGRI NIH HHS R01 HG009124NHGRI NIH HHS R01 HG010883NHGRI NIH HHS R01 HG011883NHGRI NIH HHS R01 HG012927NICHD NIH HHS R01 HD088558NIGMS NIH HHS R01 GM104496NIGMS NIH HHS R01 GM126553NIGMS NIH HHS R01 GM144960
6 · The paper itself

Abstract

Spatial transcriptomic studies are becoming increasingly common and large, posing important statistical and computational challenges for many analytic tasks. Here, we present SPARK-X, a non-parametric method for rapid and effective detection of spatially expressed genes in large spatial transcriptomic studies. SPARK-X not only produces effective type I error control and high power but also brings orders of magnitude computational savings. We apply SPARK-X to analyze three large datasets, one of which is only analyzable by SPARK-X. In these data, SPARK-X identifies many spatially expressed genes including those that are spatially expressed within the same cell type, revealing new biological insights.

Indexed as

AlgorithmsModels, Spatial InteractionTranscriptomeAnimalsCerebellumComputer SimulationDatasets as TopicFemaleGene Expression RegulationHumansMiceOlfactory BulbOvarian NeoplasmsRNA, MessengerSingle-Cell AnalysisRNA, MessengerCovariance testHDSTNon-parametric modelingSE analysisSlide-seqSPARKSPARK-XSpatial expression patternSpatial transcriptomics

Identifiers

PMID34154649
PMCPMC8218388

What OpenQuestion 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 OpenQuestion graph.