Evidence map›Paper›PMID 36494337›Full record

ArticleNature communications2022

Interpretable and tractable models of transcriptional noise for the rational design of single-molecule quantification experiments.

Gennady Gorin, John J Vastola, Meichen Fang, Lior Pachter

Abstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Article
  2. Article
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  4. Learning stochastic processes with intrinsic noise from cross-sectional biological data.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
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  12. Dissection and integration of bursty transcriptional dynamics for complex systems.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. The specious art of single-cell genomics.PLoS computational biology · 2023
    Article
  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

4 authors.

Gennady Gorin *Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, 91125, USA.ORCID http://orcid.org/0000-0001-6097-2029
John J Vastola *Department of Neurobiology, Harvard Medical School, Boston, MA, 02115, USA.ORCID http://orcid.org/0000-0002-5625-2106
Meichen FangDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, 91125, USA.ORCID http://orcid.org/0000-0002-8217-0710
Lior PachterDivision of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA, 91125, USA. lpachter@caltech.edu.ORCID http://orcid.org/0000-0002-9164-6231

Funding

Generation of novel cell type specific mouse genetic toolsU19MH114830 · NIMH · ALLEN INSTITUTE · PI NGAI, JOHN J. · 2017 to 2021
$64.7M
National Science Foundation (NSF) DMS 1562078NIMH NIH HHS U19 MH114830U.S. Department of Health & Human Services | National Institutes of Health (NIH) U19MH114830
6 · The paper itself

Abstract

The question of how cell-to-cell differences in transcription rate affect RNA count distributions is fundamental for understanding biological processes underlying transcription. Answering this question requires quantitative models that are both interpretable (describing concrete biophysical phenomena) and tractable (amenable to mathematical analysis). This enables the identification of experiments which best discriminate between competing hypotheses. As a proof of principle, we introduce a simple but flexible class of models involving a continuous stochastic transcription rate driving a discrete RNA transcription and splicing process, and compare and contrast two biologically plausible hypotheses about transcription rate variation. One assumes variation is due to DNA experiencing mechanical strain, while the other assumes it is due to regulator number fluctuations. We introduce a framework for numerically and analytically studying such models, and apply Bayesian model selection to identify candidate genes that show signatures of each model in single-cell transcriptomic data from mouse glutamatergic neurons.

Indexed as

Gene Expression ProfilingRNAAnimalsBayes TheoremMiceModels, BiologicalStochastic ProcessesRNA

Identifiers

PMID36494337
PMCPMC9734650

What OpenQuestion holds

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LicenceCC BY
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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.