Evidence map›Paper›PMID 19180177›Full record

ArticlePLoS computational biology2009

A factor graph nested effects model to identify networks from genetic perturbations.

Charles J Vaske, Carrie House, Truong Luu, Bryan Frank, Chen-Hsiang Yeang, Norman H Lee, Joshua M Stuart

Abstract read
In one paragraph

Article in PLoS computational biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 1 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

23 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Context-Specific Nested Effects Models.Journal of computational biology : a journal of computational molecular cell biology · 2020
    Article
  3. Article
  4. Article
  5. Bioinformatics challenges and perspectives when studying the effect of epigenetic modifications on alternative splicing.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
    Review
  6. DRUG-NEM: Optimizing drug combinations using single-cell perturbation response to account for intratumoral heterogeneity.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  7. Context-Specific Nested Effects Models.Research in computational molecular biology : ... Annual International Conference, RECOMB ... : proceedings. RECOMB (Conference : 2005- ) · 2018
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Multi-omic network signatures of disease.Frontiers in genetics · 2014
    Article
  14. Considering unknown unknowns: reconstruction of nonconfoundable causal relations in biological networks.Journal of computational biology : a journal of computational molecular cell biology · 2013
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

7 authors.

Charles J VaskeBiomolecular Engineering Department, University of California Santa Cruz, Santa Cruz, California, United States of America.
Carrie House
Truong Luu
Bryan Frank
Chen-Hsiang Yeang
Norman H Lee
Joshua M Stuart

Funding

Mapping Gene Networks in Colon CancerR01CA120316 · NCI · GEORGE WASHINGTON UNIVERSITY · PI LEE, NORMAN H · 2007 to 2010
$1.6M
NCI NIH HHS CA120316NCI NIH HHS R01 CA120316
6 · The paper itself

Abstract

Complex phenotypes such as the transformation of a normal population of cells into cancerous tissue result from a series of molecular triggers gone awry. We describe a method that searches for a genetic network consistent with expression changes observed under the knock-down of a set of genes that share a common role in the cell, such as a disease phenotype. The method extends the Nested Effects Model of Markowetz et al. (2005) by using a probabilistic factor graph to search for a network representing interactions among these silenced genes. The method also expands the network by attaching new genes at specific downstream points, providing candidates for subsequent perturbations to further characterize the pathway. We investigated an extension provided by the factor graph approach in which the model distinguishes between inhibitory and stimulatory interactions. We found that the extension yielded significant improvements in recovering the structure of simulated and Saccharomyces cerevisae networks. We applied the approach to discover a signaling network among genes involved in a human colon cancer cell invasiveness pathway. The method predicts several genes with new roles in the invasiveness process. We knocked down two genes identified by our approach and found that both knock-downs produce loss of invasive potential in a colon cancer cell line. Nested effects models may be a powerful tool for inferring regulatory connections and genes that operate in normal and disease-related processes.

Indexed as

Gene Expression RegulationGene Expression Regulation, NeoplasticGene SilencingAlgorithmsColonic NeoplasmsComputational BiologyComputer SimulationData Interpretation, StatisticalGene Regulatory NetworksHT29 CellsHumansModels, GeneticNeoplasm InvasivenessNormal DistributionOligonucleotide Array Sequence AnalysisSaccharomyces cerevisiae

Identifiers

PMID19180177
PMCPMC2613752

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.