Evidence map›Paper›PMID 39099456›Full record

ArticleDevelopment (Cambridge, England)2024

Open-source, high-throughput targeted in situ transcriptomics for developmental and tissue biology.

Hower Lee, Christoffer Mattsson Langseth, Sergio Marco Salas, Sanem Sariyar, Andreas Metousis, Eneritz Rueda-Alaña, Christina Bekiari, Emma Lundberg, Fernando Garcı A-Moreno, Marco Grillo and 1 more

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. 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

11 authors.

Hower LeeScience for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, 171 65 Solna, Sweden.ORCID 0000-0002-8781-3623
Christoffer Mattsson LangsethScience for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, 171 65 Solna, Sweden.ORCID 0000-0003-2230-8594
Sergio Marco SalasScience for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, 171 65 Solna, Sweden.ORCID 0000-0002-4636-0322
Sanem SariyarScience for Life Laboratory, Department of Protein Science, KTH - Royal Institute of Technology, 17165Stockholm, Sweden.ORCID 0000-0003-0735-5595
Andreas MetousisScience for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, 171 65 Solna, Sweden.ORCID 0000-0002-1043-6591
Eneritz Rueda-AlañaAchucarro Basque Center for Neuroscience, Scientific Park of the University of the Basque Country (UPV/EHU), 48940 Leioa, Spain.ORCID 0000-0003-3045-4970
Christina BekiariScience for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, 171 65 Solna, Sweden.ORCID 0009-0006-7735-9830
Emma LundbergScience for Life Laboratory, Department of Protein Science, KTH - Royal Institute of Technology, 17165Stockholm, Sweden.ORCID 0000-0001-7034-0850
Fernando Garcı A-MorenoAchucarro Basque Center for Neuroscience, Scientific Park of the University of the Basque Country (UPV/EHU), 48940 Leioa, Spain.ORCID 0000-0001-9048-4237
Marco GrilloScience for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, 171 65 Solna, Sweden.ORCID 0000-0003-2155-0645
Mats NilssonScience for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, 171 65 Solna, Sweden.ORCID 0000-0001-9985-0387

Funding

Cancerfonden CAN 2021/1726Chan Zuckerberg InitiativeEASI genomics TNAErling-Perssons StiftelseEuropean Advanced infraStructure for Innovative Genomics PID14596Eusko JaurlaritzaEusko Jaurlaritza PIBA 2020\_1\_0057Familjen Erling-Perssons StiftelseIkerbasque, Basque Foundation for ScienceKnut och Alice Wallenbergs Stiftelse KAW 2018.0172Ministerio de Ciencia e InnovacionMinisterio de Ciencia e Innovación MICNN PGC2018-096173-A-I00Silicon Valley Community FoundationStockholms UniversitetVetenskapsrådet 2019-01238
6 · The paper itself

Abstract

Multiplexed spatial profiling of mRNAs has recently gained traction as a tool to explore the cellular diversity and the architecture of tissues. We propose a sensitive, open-source, simple and flexible method for the generation of in situ expression maps of hundreds of genes. We use direct ligation of padlock probes on mRNAs, coupled with rolling circle amplification and hybridization-based in situ combinatorial barcoding, to achieve high detection efficiency, high-throughput and large multiplexing. We validate the method across a number of species and show its use in combination with orthogonal methods such as antibody staining, highlighting its potential value for developmental and tissue biology studies. Finally, we provide an end-to-end computational workflow that covers the steps of probe design, image processing, data extraction, cell segmentation, clustering and annotation of cell types. By enabling easier access to high-throughput spatially resolved transcriptomics, we hope to encourage a diversity of applications and the exploration of a wide range of biological questions.

Indexed as

Gene Expression ProfilingAnimalsDevelopmental BiologyHumansIn Situ HybridizationMiceRNA, MessengerTranscriptomeRNA, MessengerIn situ hybridizationMulti-omicsMultiplex imagingOpen sourcePadlock probesSpatial transcriptomics

Identifiers

PMID39099456
PMCPMC11385644

What OpenQuestion holds

Textmetadata
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Read underepoch 390

Registered trials

None linked

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.