Evidence map›Paper›PMID 24736851›Full record

ArticleCirculation. Cardiovascular genetics2014

Identification of functional modules by integration of multiple data sources using a Bayesian network classifier.

Jinlian Wang, Yiming Zuo, Lun Liu, Yangao Man, Mahlet G Tadesse, Habtom W Ressom

Open access · greenAbstract read
In one paragraph

Article in Circulation. Cardiovascular genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 36% of its field
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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

6 authors at 2 institutions in 2 countries.

Jinlian WangLombardi Comprehensive Cancer Center, Georgetown University Medical Center, Washington, DC.
Yiming Zuo
Lun Liu
Yangao Man
Mahlet G Tadesse
Habtom W Ressom
National Engineering Research Center for Information Technology in Agriculture · CNJackson Foundation · US

Funding

Analysis of LC-MS data to identify peptide and glycan biomarkers for hepatocellulR01CA143420 · NCI · GEORGETOWN UNIVERSITY · PI RESSOM, HABTOM W · 2010 to 2014
$1.4M
Quantitative analysis of LC-MS data for peptide and glycan biomarker discoveryR01GM086746 · NIGMS · GEORGETOWN UNIVERSITY · PI RESSOM, HABTOM W · 2010 to 2014
$1.3M
NCI NIH HHS R01 CA143420NCI NIH HHS R01CA143420NIGMS NIH HHS R01 GM086746NIGMS NIH HHS R01GM086746
6 · The paper itself

Abstract

backgroundPrediction of functional modules is indispensable for detecting protein deregulation in human complex diseases such as cancer. Bayesian network is one of the most commonly used models to integrate heterogeneous data from multiple sources such as protein domain, interactome, functional annotation, genome-wide gene expression, and the literature. METHODS AND

resultsIn this article, we present a Bayesian network classifier that is customized to (1) increase the ability to integrate diverse information from different sources, (2) effectively predict protein-protein interactions, (3) infer aberrant networks with scale-free and small-world properties, and (4) group molecules into functional modules or pathways based on the primary function and biological features. Application of this model in discovering protein biomarkers of hepatocellular carcinoma leads to the identification of functional modules that provide insights into the mechanism of the development and progression of hepatocellular carcinoma. These functional modules include cell cycle deregulation, increased angiogenesis (eg, vascular endothelial growth factor, blood vessel morphogenesis), oxidative metabolic alterations, and aberrant activation of signaling pathways involved in cellular proliferation, survival, and differentiation.

conclusionsThe discoveries and conclusions derived from our customized Bayesian network classifier are consistent with previously published results. The proposed approach for determining Bayesian network structure facilitates the integration of heterogeneous data from multiple sources to elucidate the mechanisms of complex diseases.

Indexed as

Databases, GeneticProtein Interaction MapsBayes TheoremCarcinoma, HepatocellularComputational BiologyGene Regulatory NetworksHumansLiver NeoplasmsProteinsProteinscomputational biologygene expressiongeneticsgenomicsmodels, statisticalprotein interaction domains and motifssystems biology

Identifiers

PMID24736851
PMCPMC4079061
OpenAlexW2100347830

What OpenQuestion holds

Textmetadata
LicenceTDM
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.