Evidence map›Paper›PMID 24681693›Full record

ArticleNature methods2014

Transcriptional profiling of cells sorted by RNA abundance.

Sandy Klemm, Stefan Semrau, Kay Wiebrands, Dylan Mooijman, Dina A Faddah, Rudolf Jaenisch, Alexander van Oudenaarden

Abstract read
In one paragraph

Article in Nature methods, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Injury polarized CD4Redox biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Isolation of intact RNA from murine CD4Journal of immunological methods · 2018
    Article
  13. Transcriptome Analysis of Mycobacteria-Specific CD4Journal of immunology (Baltimore, Md. : 1950) · 2017
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

7 authors.

Sandy Klemm *Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States.
Stefan Semrau *Department of Physics, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States.
Kay Wiebrands *Hubrecht Institute - Royal Netherlands Academy of Arts and Sciences, Utrecht, The Netherlands.
Dylan MooijmanHubrecht Institute - Royal Netherlands Academy of Arts and Sciences, Utrecht, The Netherlands.
Dina A FaddahDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States.
Rudolf JaenischDepartment of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States.
Alexander van OudenaardenDepartment of Physics, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States.

Funding

TRANS-NETWORK PROJECTSU54CA143874 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI MIRNY, LEONID A · 2009 to 2013
$15.1M
GENOMIC IMPRINTING AND THE CLONING OF MICER37CA084198 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI JAENISCH, RUDOLF · 2000 to 2008
$9.2M
In Vitro Reprogramming of Somatic Cells into Pluripotent ES-like CellsR37HD045022 · NICHD · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI JAENISCH, RUDOLF · 2009 to 2017
$7.5M
Nuclear Cloning and the Reprogramming of the GenomeR01HD045022 · NICHD · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI JAENISCH, RUDOLF · 2003 to 2008
$4.7M
Stochastic gene expression in differentiation and developmentDP1CA174420 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI VAN OUDENAARDEN, ALEXANDER · 2012 to 2012
$832k
NCI NIH HHS 8 DP1 CA174420-05NCI NIH HHS DP1 CA174420NCI NIH HHS R37 CA084198NCI NIH HHS R37CA084198NCI NIH HHS U54 CA143874NCI NIH HHS U54CA143874NICHD NIH HHS HD 045022NICHD NIH HHS R37 HD045022
6 · The paper itself

Abstract

We have developed a quantitative technique for sorting cells on the basis of endogenous RNA abundance, with a molecular resolution of 10-20 transcripts. We demonstrate efficient and unbiased RNA extraction from transcriptionally sorted cells and report a high-fidelity transcriptome measurement of mouse induced pluripotent stem cells (iPSCs) isolated from a heterogeneous reprogramming culture. This method is broadly applicable to profiling transcriptionally distinct cellular states without requiring antibodies or transgenic fluorescent proteins.

Indexed as

Cell Culture TechniquesGene Expression ProfilingTranscription, GeneticAllelesAnimalsCellular ReprogrammingDoxycyclineEmbryonic Stem CellsFibroblastsFlow CytometryGenome-Wide Association StudyGreen Fluorescent ProteinsInduced Pluripotent Stem CellsIn Situ Hybridization, FluorescenceMiceNIH 3T3 CellsDoxycyclineGreen Fluorescent ProteinsRNARNA, Messenger

Identifiers

PMID24681693
PMCPMC4174458

What OpenQuestion holds

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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.