Evidence map›Paper›PMID 27739429›Full record

ArticleNature communications2016

Massive and parallel expression profiling using microarrayed single-cell sequencing.

Sanja Vickovic, Patrik L Ståhl, Fredrik Salmén, Sarantis Giatrellis, Jakub Orzechowski Westholm, Annelie Mollbrink, José Fernández Navarro, Joaquin Custodio, Magda Bienko, Lesley-Ann Sutton and 3 more

Abstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing 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

26 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Spatial Transcriptomics in Kidney Tissue.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  8. Review
  9. Towards precision medicine in lymphoid malignancies.Journal of internal medicine · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Deciphering Brain Complexity Using Single-cell Sequencing.Genomics, proteomics & bioinformatics · 2019
    Review
  20. Article
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

13 authors.

Sanja VickovicScience for Life Laboratory, Division of Gene Technology, School of Biotechnology, KTH Royal Institute of Technology, SE-114 28 Stockholm, Sweden.ORCID http://orcid.org/0000-0003-0985-9885
Patrik L StåhlDepartment of Cell and Molecular Biology, Karolinska Institute, SE-171 77 Stockholm, Sweden.
Fredrik SalménScience for Life Laboratory, Division of Gene Technology, School of Biotechnology, KTH Royal Institute of Technology, SE-114 28 Stockholm, Sweden.
Sarantis GiatrellisDepartment of Cell and Molecular Biology, Karolinska Institute, SE-171 77 Stockholm, Sweden.
Jakub Orzechowski WestholmScience for Life Laboratory, Department of Biochemistry and Biophysics, Stockholm University, SE-106 91 Stockholm, Sweden.
Annelie MollbrinkScience for Life Laboratory, Department of Medical Biochemistry and Biophysics, Karolinska Institute, SE-171 77 Stockholm, Sweden.
José Fernández NavarroDepartment of Cell and Molecular Biology, Karolinska Institute, SE-171 77 Stockholm, Sweden.
Joaquin CustodioScience for Life Laboratory, Department of Medical Biochemistry and Biophysics, Karolinska Institute, SE-171 77 Stockholm, Sweden.
Magda BienkoScience for Life Laboratory, Department of Medical Biochemistry and Biophysics, Karolinska Institute, SE-171 77 Stockholm, Sweden.
Lesley-Ann SuttonScience for Life Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, SE-751 85 Uppsala, Sweden.
Richard RosenquistScience for Life Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, SE-751 85 Uppsala, Sweden.
Jonas FrisénDepartment of Cell and Molecular Biology, Karolinska Institute, SE-171 77 Stockholm, Sweden.
Joakim LundebergScience for Life Laboratory, Division of Gene Technology, School of Biotechnology, KTH Royal Institute of Technology, SE-114 28 Stockholm, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single-cell transcriptome analysis overcomes problems inherently associated with averaging gene expression measurements in bulk analysis. However, single-cell analysis is currently challenging in terms of cost, throughput and robustness. Here, we present a method enabling massive microarray-based barcoding of expression patterns in single cells, termed MASC-seq. This technology enables both imaging and high-throughput single-cell analysis, characterizing thousands of single-cell transcriptomes per day at a low cost (0.13 USD/cell), which is two orders of magnitude less than commercially available systems. Our novel approach provides data in a rapid and simple way. Therefore, MASC-seq has the potential to accelerate the study of subtle clonal dynamics and help provide critical insights into disease development and other biological processes.

Indexed as

AnimalsBiotechnologyCells, CulturedFlow CytometryGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansLeukemia, Lymphocytic, Chronic, B-CellMCF-7 CellsMiceNIH 3T3 CellsSingle-Cell Analysis

Identifiers

PMID27739429
PMCPMC5067491

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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.