Evidence map›Paper›PMID 29801503›Full record

ArticleBMC systems biology2018

SCNS: a graphical tool for reconstructing executable regulatory networks from single-cell genomic data.

Steven Woodhouse, Nir Piterman, Christoph M Wintersteiger, Berthold Göttgens, Jasmin Fisher

Abstract read
In one paragraph

Article in BMC systems biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 2 pooled it
–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

47 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Multi-omic network inference from time-series data.NPJ systems biology and applications · 2025
    Article
  5. Automated model refinement using perturbation-observation pairs.NPJ systems biology and applications · 2025
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  16. Canalizing kernel for cell fate determination.Briefings in bioinformatics · 2024
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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

5 authors.

Steven WoodhouseDepartment of Hematology, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK.
Nir PitermanDepartment of Informatics, University of Leicester, University Road, Leicester, LE1 7RH, UK.
Christoph M WintersteigerMicrosoft Research Cambridge, 21 Station Road, Cambridge, CB1 2FB, UK.
Berthold GöttgensDepartment of Hematology, Cambridge Institute for Medical Research, University of Cambridge, Cambridge, CB2 0XY, UK. bg200@cam.ac.uk.
Jasmin FisherMicrosoft Research Cambridge, 21 Station Road, Cambridge, CB1 2FB, UK. jf416@cam.ac.uk.

Funding

Medical Research Council MC_PC_12009Wellcome Trust
6 · The paper itself

Abstract

backgroundReconstruction of executable mechanistic models from single-cell gene expression data represents a powerful approach to understanding developmental and disease processes. New ambitious efforts like the Human Cell Atlas will soon lead to an explosion of data with potential for uncovering and understanding the regulatory networks which underlie the behaviour of all human cells. In order to take advantage of this data, however, there is a need for general-purpose, user-friendly and efficient computational tools that can be readily used by biologists who do not have specialist computer science knowledge.

resultsThe Single Cell Network Synthesis toolkit (SCNS) is a general-purpose computational tool for the reconstruction and analysis of executable models from single-cell gene expression data. Through a graphical user interface, SCNS takes single-cell qPCR or RNA-sequencing data taken across a time course, and searches for logical rules that drive transitions from early cell states towards late cell states. Because the resulting reconstructed models are executable, they can be used to make predictions about the effect of specific gene perturbations on the generation of specific lineages.

conclusionsSCNS should be of broad interest to the growing number of researchers working in single-cell genomics and will help further facilitate the generation of valuable mechanistic insights into developmental, homeostatic and disease processes.

Indexed as

Computer GraphicsGene Regulatory NetworksSingle-Cell AnalysisAlgorithmsGenomicsUser-Computer InterfaceDevelopmental biologyExecutable biologyGene regulatory networksSingle cell

Identifiers

PMID29801503
PMCPMC5970485

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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.