Evidence map›Paper›PMID 24500204›Full record

ArticleNucleic acids research2014

EDDY: a novel statistical gene set test method to detect differential genetic dependencies.

Sungwon Jung, Seungchan Kim

Abstract readEvaluation Study
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Systems Analysis of the Human Pulmonary Arterial Hypertension Lung Transcriptome.American journal of respiratory cell and molecular biology · 2019
    Article
  6. End Stage Takes Center Stage in Pulmonary Arterial Hypertension.American journal of respiratory cell and molecular biology · 2019
    Article
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. DIFFERENTIAL PATHWAY DEPENDENCY DISCOVERY ASSOCIATED WITH DRUG RESPONSE ACROSS CANCER CELL LINES.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2017
    Article
  14. Review
  15. Article
  16. Article
  17. KNOWLEDGE-ASSISTED APPROACH TO IDENTIFY PATHWAYS WITH DIFFERENTIAL DEPENDENCIES.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2016
    Article
  18. Article
  19. 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

2 authors.

Sungwon JungIntegrated Cancer Genomics Division, Biocomputing Unit, Translational Genomics Research Institute, 445 North 5th Street, Phoenix, AZ 85004, USA.
Seungchan Kim

Funding

Systematic Development of Novel, Druggable Cancer TargetsU01CA168397 · NCI · TRANSLATIONAL GENOMICS RESEARCH INST · PI BERENS, MICHAEL E. · 2012 to 2016
$4.1M
NCI NIH HHS 1U01CA168397-01PHS HHS 29XS195
6 · The paper itself

Abstract

Identifying differential features between conditions is a popular approach to understanding molecular features and their mechanisms underlying a biological process of particular interest. Although many tests for identifying differential expression of gene or gene sets have been proposed, there was limited success in developing methods for differential interactions of genes between conditions because of its computational complexity. We present a method for Evaluation of Dependency DifferentialitY (EDDY), which is a statistical test for differential dependencies of a set of genes between two conditions. Unlike previous methods focused on differential expression of individual genes or correlation changes of individual gene-gene interactions, EDDY compares two conditions by evaluating the probability distributions of dependency networks from genes. The method has been evaluated and compared with other methods through simulation studies, and application to glioblastoma multiforme data resulted in informative cancer and glioblastoma multiforme subtype-related findings. The comparison with Gene Set Enrichment Analysis, a differential expression-based method, revealed that EDDY identifies the gene sets that are complementary to those identified by Gene Set Enrichment Analysis. EDDY also showed much lower false positives than Gene Set Co-expression Analysis, a method based on correlation changes of individual gene-gene interactions, thus providing more informative results. The Java implementation of the algorithm is freely available to noncommercial users. Download from: http://biocomputing.tgen.org/software/EDDY.

Indexed as

Gene Regulatory NetworksCyclin-Dependent Kinase Inhibitor p16Data Interpretation, StatisticalGene ExpressionGlioblastomaHumansTumor Suppressor Protein p53Cyclin-Dependent Kinase Inhibitor p16TP53 protein, humanTumor Suppressor Protein p53

Identifiers

PMID24500204
PMCPMC3985670

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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.