Evidence map›Paper›PMID 33138772›Full record

ArticleBMC genomics2020

Functional module detection through integration of single-cell RNA sequencing data with protein-protein interaction networks.

Florian Klimm, Enrique M Toledo, Thomas Monfeuga, Fang Zhang, Charlotte M Deane, Gesine Reinert

Abstract read
In one paragraph

Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Review
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  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. NetMix: A Network-Structured Mixture Model for Reduced-Bias Estimation of Altered Subnetworks.Journal of computational biology : a journal of computational molecular cell biology · 2021
    Article
  10. 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

6 authors.

Florian KlimmDepartment of Mathematics, Imperial College London, London, SW7 2AZ, UK. f.klimm@gmail.com.
Enrique M ToledoDiscovery Technology and Genomics, Novo Nordisk Research Centre Oxford, Oxford, OX3 7FZ, UK.
Thomas MonfeugaDiscovery Technology and Genomics, Novo Nordisk Research Centre Oxford, Oxford, OX3 7FZ, UK.
Fang ZhangDiscovery Technology and Genomics, Novo Nordisk Research Centre Oxford, Oxford, OX3 7FZ, UK.
Charlotte M DeaneDepartment of Statistics, University of Oxford, Oxford, OX1 3LB, UK.
Gesine ReinertDepartment of Statistics, University of Oxford, Oxford, OX1 3LB, UK.

Funding

Engineering and Physical Sciences Research Council EP/N014529/1Engineering and Physical Sciences Research Council EP/R018472/1Engineering and Physical Sciences Research Council EP/R513295/1
6 · The paper itself

Abstract

backgroundRecent advances in single-cell RNA sequencing have allowed researchers to explore transcriptional function at a cellular level. In particular, single-cell RNA sequencing reveals that there exist clusters of cells with similar gene expression profiles, representing different transcriptional states.

resultsIn this study, we present SCPPIN, a method for integrating single-cell RNA sequencing data with protein-protein interaction networks that detects active modules in cells of different transcriptional states. We achieve this by clustering RNA-sequencing data, identifying differentially expressed genes, constructing node-weighted protein-protein interaction networks, and finding the maximum-weight connected subgraphs with an exact Steiner-tree approach. As case studies, we investigate two RNA-sequencing data sets from human liver spheroids and human adipose tissue, respectively. With SCPPIN we expand the output of differential expressed genes analysis with information from protein interactions. We find that different transcriptional states have different subnetworks of the protein-protein interaction networks significantly enriched which represent biological pathways. In these pathways, SCPPIN identifies proteins that are not differentially expressed but have a crucial biological function (e.g., as receptors) and therefore reveals biology beyond a standard differential expressed gene analysis.

conclusionsThe introduced SCPPIN method can be used to systematically analyse differentially expressed genes in single-cell RNA sequencing data by integrating it with protein interaction data. The detected modules that characterise each cluster help to identify and hypothesise a biological function associated to those cells. Our analysis suggests the participation of unexpected proteins in these pathways that are undetectable from the single-cell RNA sequencing data alone. The techniques described here are applicable to other organisms and tissues.

Indexed as

Protein Interaction MapsRNACluster AnalysisGene Expression ProfilingGene Regulatory NetworksHumansSequence Analysis, RNARNA

Identifiers

PMID33138772
PMCPMC7607865

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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.