Evidence map›Paper›PMID 28675924›Full record

ArticleStatistics in medicine2017

A statistical framework for biomedical literature mining.

Dongjun Chung, Andrew Lawson, W Jim Zheng

Abstract read
In one paragraph

Article in Statistics in medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Sparse Linear Discriminant Analysis using the Prior-Knowledge-Guided Block Covariance Matrix.Chemometrics and intelligent laboratory systems : an international journal sponsored by the Chemometrics Society · 2020
    Article
  2. Article
  3. Article
  4. Review
  5. 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

3 authors.

Dongjun ChungDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, U.S.A.ORCID http://orcid.org/0000-0002-8072-5671
Andrew LawsonDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, U.S.A.
W Jim ZhengSchool of Biomedical Informatics, The University of Texas Health Science Center at Houston, Houston, Texas, U.S.A.

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND N. DUBOIS · 2009 to 2026
$42.7M
Statistical Models for Genetic Studies, Using Network and Integrative AnalysisR01GM122078 · NIGMS · OHIO STATE UNIVERSITY · PI CHUNG, DONGJUN · 2016 to 2020
$1.9M
Bridging Genomics and Medicine by Ontology FingerprintsR56LM010680 · NLM · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI LAWSON, ANDREW B. · 2012 to 2013
$499k
Algorithms for Literature-Guided Multi-Platform Identification of Cancer SubtypesR21CA209848 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI CHUNG, DONGJUN, KELEMEN, LINDA E · 2016 to 2017
$358k
NCI NIH HHS P30 CA138313NCI NIH HHS R21 CA209848NIGMS NIH HHS R01 GM122078NLM NIH HHS R56 LM010680
6 · The paper itself

Abstract

In systems biology, it is of great interest to identify new genes that were not previously reported to be associated with biological pathways related to various functions and diseases. Identification of these new pathway-modulating genes does not only promote understanding of pathway regulation mechanisms but also allow identification of novel targets for therapeutics. Recently, biomedical literature has been considered as a valuable resource to investigate pathway-modulating genes. While the majority of currently available approaches are based on the co-occurrence of genes within an abstract, it has been reported that these approaches show only sub-optimal performances because 70% of abstracts contain information only for a single gene. To overcome such limitation, we propose a novel statistical framework based on the concept of ontology fingerprint that uses gene ontology to extract information from large biomedical literature data. The proposed framework simultaneously identifies pathway-modulating genes and facilitates interpreting functions of these new genes. We also propose a computationally efficient posterior inference procedure based on Metropolis-Hastings within Gibbs sampler for parameter updates and the poor man's reversible jump Markov chain Monte Carlo approach for model selection. We evaluate the proposed statistical framework with simulation studies, experimental validation, and an application to studies of pathway-modulating genes in yeast. The R implementation of the proposed model is currently available at https://dongjunchung.github.io/bayesGO/. Copyright © 2017 John Wiley & Sons, Ltd.

Indexed as

Bayes TheoremGene OntologyAlgorithmsBiometryComputer SimulationData MiningDNA FingerprintingGenesHumansMarkov ChainsMonte Carlo MethodReproducibility of ResultsSaccharomyces cerevisiaeSphingolipidsSystems BiologySphingolipidsBayesian hierarchical modelbiological pathwaygene ontologyliterature searchontology fingerprint

Identifiers

PMID28675924
PMCPMC5657248

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.