Evidence map›Paper›PMID 24248345›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

RNA-sequencing from single nuclei.

Rashel V Grindberg, Joyclyn L Yee-Greenbaum, Michael J McConnell, Mark Novotny, Andy L O'Shaughnessy, Georgina M Lambert, Marcos J Araúzo-Bravo, Jun Lee, Max Fishman, Gillian E Robbins and 6 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05942339 (Study on Preliminary Safety and Efficacy of the ARC Therapy Using the ARC-IM Lumbar System to Support Mobility in People With Chronic Spinal Cord Injury), which is not on this map. Cited by 243 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
243citing papers in PubMed, 1 pooled it
6.7field-weighted citation impact, top 2% 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.

NCT05942339 narecruitingnot on this mapstarted 2023, after this paper: background citation

Study on Preliminary Safety and Efficacy of the ARC Therapy Using the ARC-IM Lumbar System to Support Mobility in People With Chronic Spinal Cord Injury

TypeinterventionalSponsorEcole Polytechnique Fédérale de LausanneRan2023 to 2027Enrolled8ConditionsSpinal Cord InjuriesArmsProcedure/Surgery
3 · Its place in the literature

Who cites it

243 citing papers in PubMed, 1 synthesis or guideline pooled it, 448 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. 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
  8. Article
  9. Article
  10. Review
  11. Article
  12. Decoding neurodegeneration one cell at a time.The Journal of clinical investigation · 2026
    Review
  13. Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

183 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

16 authors at 6 institutions in 3 countries.

Rashel V GrindbergJ. Craig Venter Institute, San Diego, CA 92121.
Joyclyn L Yee-Greenbaum
Michael J McConnell
Mark Novotny
Andy L O'Shaughnessy
Georgina M Lambert
Marcos J Araúzo-Bravo
Jun Lee
Max Fishman
Gillian E Robbins
Xiaoying Lin
Pratap Venepally
Jonathan H Badger
David W Galbraith
Fred H Gage
Roger S Lasken
J. Craig Venter Institute · USUniversity of Arizona · USMax Planck Institute for Molecular Biomedicine · DESalk Institute for Biological Studies · USThermo Fisher Scientific (Norway) · NOUniversity of Virginia · US

Funding

Single-Cell Approaches to Reveal How Jumping Genes Individualize Neural CircuitsR01MH095741 · NIMH · SALK INSTITUTE FOR BIOLOGICAL STUDIES · PI GAGE, FRED H · 2011 to 2015
$6.5M
WHOLE GENOME AMPLIFICATION FOR RAPID LOW COST GENOTYPINGR01HG003647 · NHGRI · J. CRAIG VENTER INSTITUTE, INC. · PI LASKEN, ROGER SENDER · 2005 to 2013
$3.6M
Transcriptomics from Single Circulating Tumor CellsRC1HG005471 · NHGRI · J. CRAIG VENTER INSTITUTE, INC. · PI LASKEN, ROGER SENDER · 2009 to 2010
$998k
Cell-specific analysis of transcription and epigenomic status in PDACR21CA164690 · NCI · UNIVERSITY OF ARIZONA · PI DOETSCHMAN, THOMAS, GALBRAITH, DAVID W · 2012 to 2013
$351k
NCI NIH HHS NIH-NCI R21-CA164690NCI NIH HHS R21 CA164690NHGRI NIH HHS NIH-1 RC1 HG005471NHGRI NIH HHS NIH 2R01 HG003647NHGRI NIH HHS R01 HG003647NHGRI NIH HHS RC1 HG005471NIMH NIH HHS R01 MH095741NIMH NIH HHS TRO1MH095741
6 · The paper itself

Abstract

It has recently been established that synthesis of double-stranded cDNA can be done from a single cell for use in DNA sequencing. Global gene expression can be quantified from the number of reads mapping to each gene, and mutations and mRNA splicing variants determined from the sequence reads. Here we demonstrate that this method of transcriptomic analysis can be done using the extremely low levels of mRNA in a single nucleus, isolated from a mouse neural progenitor cell line and from dissected hippocampal tissue. This method is characterized by excellent coverage and technical reproducibility. On average, more than 16,000 of the 24,057 mouse protein-coding genes were detected from single nuclei, and the amount of gene-expression variation was similar when measured between single nuclei and single cells. Several major advantages of the method exist: first, nuclei, compared with whole cells, have the advantage of being easily isolated from complex tissues and organs, such as those in the CNS. Second, the method can be widely applied to eukaryotic species, including those of different kingdoms. The method also provides insight into regulatory mechanisms specific to the nucleus. Finally, the method enables dissection of regulatory events at the single-cell level; pooling of 10 nuclei or 10 cells obscures some of the variability measured in transcript levels, implying that single nuclei and cells will be extremely useful in revealing the physiological state and interconnectedness of gene regulation in a manner that avoids the masking inherent to conventional transcriptomics using bulk cells or tissues.

Indexed as

AnimalsCell NucleusDentate GyrusEmbryonic Stem CellsFlow CytometryGene Expression ProfilingHigh-Throughput Nucleotide SequencingMiceMicromanipulationMicroscopy, FluorescenceNeural Stem Cellsdeep sequencingnuclear RNAwhole cell RNA

Identifiers

PMID24248345
PMCPMC3856806
OpenAlexW2112630596

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.