Evidence map›Paper›PMID 25086649›Full record

ArticleNature biotechnology2014

Low-coverage single-cell mRNA sequencing reveals cellular heterogeneity and activated signaling pathways in developing cerebral cortex.

Alex A Pollen, Tomasz J Nowakowski, Joe Shuga, Xiaohui Wang, Anne A Leyrat, Jan H Lui, Nianzhen Li, Lukasz Szpankowski, Brian Fowler, Peilin Chen and 20 more

Open access · greenAbstract read
In one paragraph

Article in Nature biotechnology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 485 papers.

0numbers the graph read from it
0cells of the map it votes in
485citing papers in PubMed
36.6field-weighted citation impact, top 1% of its field
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

485 citing papers in PubMed, 989 citations in OpenAlex.

  1. Article
  2. Article
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  5. Single-cell RNA sequencing in stroke and traumatic brain injury: Current achievements, challenges and future perspectives on transcriptomic profiling.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Modern Mining: The Role of Single-cell RNA Sequencing in Advancing Neuroscience Research.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Cell-Based Immuno-Biosensors Using Microfluidics.Sensors (Basel, Switzerland) · 2026
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors at 3 institutions in 1 country.

Alex A Pollen1] Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, California, USA. [2] Department of Neurology, University of California, San Francisco, San Francisco, California, USA. [3].
Tomasz J Nowakowski1] Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, California, USA. [2] Department of Neurology, University of California, San Francisco, San Francisco, California, USA. [3].
Joe Shuga1] Fluidigm Corporation, South San Francisco, California, USA. [2].
Xiaohui Wang1] Fluidigm Corporation, South San Francisco, California, USA. [2].
Anne A LeyratFluidigm Corporation, South San Francisco, California, USA.
Jan H Lui1] Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, California, USA. [2] Department of Neurology, University of California, San Francisco, San Francisco, California, USA.
Nianzhen LiFluidigm Corporation, South San Francisco, California, USA.
Lukasz SzpankowskiFluidigm Corporation, South San Francisco, California, USA.
Brian FowlerFluidigm Corporation, South San Francisco, California, USA.
Peilin ChenFluidigm Corporation, South San Francisco, California, USA.
Naveen RamalingamFluidigm Corporation, South San Francisco, California, USA.
Gang SunFluidigm Corporation, South San Francisco, California, USA.
Myo ThuFluidigm Corporation, South San Francisco, California, USA.
Michael NorrisFluidigm Corporation, South San Francisco, California, USA.
Ronald LebofskyFluidigm Corporation, South San Francisco, California, USA.
Dominique ToppaniFluidigm Corporation, South San Francisco, California, USA.
Darnell W KempFluidigm Corporation, South San Francisco, California, USA.
Michael WongFluidigm Corporation, South San Francisco, California, USA.
Barry ClerksonFluidigm Corporation, South San Francisco, California, USA.
Brittnee N JonesFluidigm Corporation, South San Francisco, California, USA.
Shiquan WuFluidigm Corporation, South San Francisco, California, USA.
Lawrence KnutssonFluidigm Corporation, South San Francisco, California, USA.
Beatriz AlvaradoFluidigm Corporation, South San Francisco, California, USA.
Jing WangFluidigm Corporation, South San Francisco, California, USA.
Lesley S WeaverFluidigm Corporation, South San Francisco, California, USA.
Andrew P MayFluidigm Corporation, South San Francisco, California, USA.
Robert C JonesFluidigm Corporation, South San Francisco, California, USA.
Marc A UngerFluidigm Corporation, South San Francisco, California, USA.
Arnold R Kriegstein1] Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, San Francisco, California, USA. [2] Department of Neurology, University of California, San Francisco, San Francisco, California, USA.
Jay A A WestFluidigm Corporation, South San Francisco, California, USA.
Fluidigm (United States) · USBroad Center · USUniversity of California, San Francisco · US

Funding

Stem Cells of the Developing Human NeocortexR01NS075998 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRIEGSTEIN, ARNOLD · 2011 to 2016
$1.8M
Molecular and cellular mechanism of MicrocephalyR01NS072630 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRIEGSTEIN, ARNOLD · 2010 to 2014
$1.6M
NINDS NIH HHS R01 NS072630NINDS NIH HHS R01NS072630NINDS NIH HHS R01 NS075998NINDS NIH HHS R01NS075998
6 · The paper itself

Abstract

Large-scale surveys of single-cell gene expression have the potential to reveal rare cell populations and lineage relationships but require efficient methods for cell capture and mRNA sequencing. Although cellular barcoding strategies allow parallel sequencing of single cells at ultra-low depths, the limitations of shallow sequencing have not been investigated directly. By capturing 301 single cells from 11 populations using microfluidics and analyzing single-cell transcriptomes across downsampled sequencing depths, we demonstrate that shallow single-cell mRNA sequencing (~50,000 reads per cell) is sufficient for unbiased cell-type classification and biomarker identification. In the developing cortex, we identify diverse cell types, including multiple progenitor and neuronal subtypes, and we identify EGR1 and FOS as previously unreported candidate targets of Notch signaling in human but not mouse radial glia. Our strategy establishes an efficient method for unbiased analysis and comparison of cell populations from heterogeneous tissue by microfluidic single-cell capture and low-coverage sequencing of many cells.

Indexed as

AnimalsCerebral CortexComputational BiologyEquipment DesignGene Expression ProfilingHumansMiceMicrofluidic Analytical TechniquesRNA, MessengerSequence Analysis, RNASignal TransductionRNA, Messenger

Identifiers

PMID25086649
PMCPMC4191988
OpenAlexW2051658465

What OpenQuestion holds

Textmetadata
LicenceTDM
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.