Evidence map›Paper›PMID 15725730›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2005

Mining genetic epidemiology data with Bayesian networks application to APOE gene variation and plasma lipid levels.

Andrei Rodin, Thomas H Mosley, Andrew G Clark, Charles F Sing, Eric Boerwinkle

Abstract read
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Trial
  2. Article
  3. Synthetic data generation with probabilistic Bayesian Networks.Mathematical biosciences and engineering : MBE · 2021
    Article
  4. Article
  5. Analysis of high-resolution 3D intrachromosomal interactions aided by Bayesian network modeling.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  6. New Algorithm and Software (BNOmics) for Inferring and Visualizing Bayesian Networks from Heterogeneous Big Biological and Genetic Data.Journal of computational biology : a journal of computational molecular cell biology · 2017
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Use of wrapper algorithms coupled with a random forests classifier for variable selection in large-scale genomic association studies.Journal of computational biology : a journal of computational molecular cell biology · 2009
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. 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.

Andrei RodinHuman Genetics Center, University of Texas Health Science Center, 1200 Herman Pressler Drive, Houston, TX 77030, USA.
Thomas H Mosley
Andrew G Clark
Charles F Sing
Eric Boerwinkle

Funding

Variable DNA sites predicting interindividual variation in health measuresP50GM065509 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SING, CHARLES · 2001 to 2011
$27.5M
Modeling DNA Diversity in Reverse Cholesterol TransportR01HL072905 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SING, CHARLES · 2003 to 2012
$5.3M
NHLBI NIH HHS R01 HL072905NIGMS NIH HHS P50 GM065509
6 · The paper itself

Abstract

There is a critical need for data-mining methods that can identify SNPs that predict among individual variation in a phenotype of interest and reverse-engineer the biological network of relationships between SNPs, phenotypes, and other factors. This problem is both challenging and important in light of the large number of SNPs in many genes of interest and across the human genome. A potentially fruitful form of exploratory data analysis is the Bayesian or Belief network. A Bayesian or Belief network provides an analytic approach for identifying robust predictors of among-individual variation in a disease endpoints or risk factor levels. We have applied Belief networks to SNP variation in the human APOE gene and plasma apolipoprotein E levels from two samples: 702 African-Americans from Jackson, MS, and 854 non-Hispanic whites from Rochester, MN. Twenty variable sites in the APOE gene were genotyped in both samples. In Jackson, MS, SNPs 4036 and 4075 were identified to influence plasma apoE levels. In Rochester, MN, SNPs 3937 and 4075 were identified to influence plasma apoE levels. All three SNPs had been previously implicated in affecting measures of lipid and lipoprotein metabolism. Like all data-mining methods, Belief networks are meant to complement traditional hypothesis-driven methods of data analysis. These results document the utility of a Belief network approach for mining large scale genotype-phenotype association data.

Indexed as

Bayes TheoremLinkage DisequilibriumModels, GeneticPolymorphism, Single NucleotideApolipoproteins EDatabases, FactualGenetics, PopulationHumansLipidsApolipoproteins ELipids

Identifiers

PMID15725730
PMCPMC1201451

What OpenQuestion holds

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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.