Evidence map›Paper›PMID 30371680›Full record

ArticleNature biotechnology2018

Identification of spatially associated subpopulations by combining scRNAseq and sequential fluorescence in situ hybridization data.

Qian Zhu, Sheel Shah, Ruben Dries, Long Cai, Guo-Cheng Yuan

Abstract read
In one paragraph

Article in Nature biotechnology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 138 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed, 2 pooled it
–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

138 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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78 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

5 authors.

Qian ZhuDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute and Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Sheel ShahDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, USA.
Ruben DriesDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute and Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.
Long CaiDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, California, USA.ORCID http://orcid.org/0000-0002-7154-5361
Guo-Cheng YuanDepartment of Biostatistics and Computational Biology, Dana-Farber Cancer Institute and Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA.ORCID http://orcid.org/0000-0002-2283-4714

Funding

Multiplex RNA imaging in single cells by superresolution microscopy& barcode FISHR01HD075605 · NICHD · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI CAI, LONG, SOMLO, GEORGE NONE · 2012 to 2016
$4.1M
Systems Biology Analysis of Human ErythropoiesisR01HL119099 · NHLBI · DANA-FARBER CANCER INST · PI ORKIN, STUART H, YUAN, GUO-CHENG · 2014 to 2018
$3.4M
In situ transcriptome profiling in single cellsUG3HL145609 · NHLBI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI CAI, LONG, YUAN, GUO-CHENG · 2018 to 2019
$750k
NHLBI NIH HHS R01 HL119099NHLBI NIH HHS UG3 HL145609NICHD NIH HHS R01 HD075605
6 · The paper itself

Abstract

How intrinsic gene-regulatory networks interact with a cell's spatial environment to define its identity remains poorly understood. We developed an approach to distinguish between intrinsic and extrinsic effects on global gene expression by integrating analysis of sequencing-based and imaging-based single-cell transcriptomic profiles, using cross-platform cell type mapping combined with a hidden Markov random field model. We applied this approach to dissect the cell-type- and spatial-domain-associated heterogeneity in the mouse visual cortex region. Our analysis identified distinct spatially associated, cell-type-independent signatures in the glutamatergic and astrocyte cell compartments. Using these signatures to analyze single-cell RNA sequencing data, we identified previously unknown spatially associated subpopulations, which were validated by comparison with anatomical structures and Allen Brain Atlas images.

Identifiers

PMID30371680
PMCPMC6488461

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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.