Evidence map›Paper›PMID 34902128›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2022

Network Analysis of Microarray Data.

Alisa Pavel, Angela Serra, Luca Cattelani, Antonio Federico, Dario Greco

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. The impact of dropouts in scRNAseq dense neighborhood analysis.Computational and structural biotechnology journal · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. Nextcast: A software suite to analyse and model toxicogenomics data.Computational and structural biotechnology journal · 2022
    Article
  7. 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

5 authors.

Alisa Pavel *Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Angela Serra *Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Luca CattelaniFaculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Antonio FedericoFaculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Dario GrecoFaculty of Medicine and Health Technology, Tampere University, Tampere, Finland. dario.greco@tuni.fi.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA microarrays are widely used to investigate gene expression. Even though the classical analysis of microarray data is based on the study of differentially expressed genes, it is well known that genes do not act individually. Network analysis can be applied to study association patterns of the genes in a biological system. Moreover, it finds wide application in differential coexpression analysis between different systems. Network based coexpression studies have for example been used in (complex) disease gene prioritization, disease subtyping, and patient stratification.In this chapter we provide an overview of the methods and tools used to create networks from microarray data and describe multiple methods on how to analyze a single network or a group of networks. The described methods range from topological metrics, functional group identification to data integration strategies, topological pathway analysis as well as graphical models.

Indexed as

Gene Regulatory NetworksAlgorithmsGene Expression ProfilingHumansOligonucleotide Array Sequence AnalysisCoexpressionDifferential coexpressionMicroarrayMultilayer networksPathways

Identifiers

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.