Evidence map›Paper›PMID 33008309›Full record

ArticleBMC bioinformatics2020

PALMER: improving pathway annotation based on the biomedical literature mining with a constrained latent block model.

Jin Hyun Nam, Daniel Couch, Willian A da Silveira, Zhenning Yu, Dongjun Chung

Abstract read
In one paragraph

Article in BMC bioinformatics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. WayFindR: investigating feedback in biological pathways.NAR genomics and bioinformatics · 2026
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5 · Who and what money

Authors and funding

5 authors.

Jin Hyun NamDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA.
Daniel CouchDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA.
Willian A da SilveiraSchool of Biological Sciences, Queen's University Belfast, Belfast, UK.
Zhenning YuDepartment of Public Health Sciences, Medical University of South Carolina, Charleston, SC, USA.
Dongjun ChungDepartment of Biomedical Informatics, The Ohio State University, Columbus, OH, USA. chung.911@osu.edu.ORCID http://orcid.org/0000-0002-8072-5671

Funding

Resource CoreP30AR072582 · NIAMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI JAMES C OATES · 2017 to 2026
$8.5M
The Genetic Basis of Opioid Dependence Vulnerablility in a Rodent ModelU01DA045300 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Christine Cheng, Dongjun Chung · 2018 to 2026
$6.1M
Statistical Models for Genetic Studies, Using Network and Integrative AnalysisR01GM122078 · NIGMS · OHIO STATE UNIVERSITY · PI CHUNG, DONGJUN · 2016 to 2020
$1.9M
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 R21 CA209848NCI NIH HHS R21-CA209848NIAMS NIH HHS P30 AR072582NIAMS NIH HHS P30-AR072582NIDA NIH HHS U01 DA045300NIDA NIH HHS U01-DA045300NIGMS NIH HHS R01 GM122078NIGMS NIH HHS R01-GM122078
6 · The paper itself

Abstract

backgroundIn systems biology, it is of great interest to identify previously unreported associations between genes. Recently, biomedical literature has been considered as a valuable resource for this purpose. While classical clustering algorithms have popularly been used to investigate associations among genes, they are not tuned for the literature mining data and are also based on strong assumptions, which are often violated in this type of data. For example, these approaches often assume homogeneity and independence among observations. However, these assumptions are often violated due to both redundancies in functional descriptions and biological functions shared among genes. Latent block models can be alternatives in this case but they also often show suboptimal performances, especially when signals are weak. In addition, they do not allow to utilize valuable prior biological knowledge, such as those available in existing databases.

resultsIn order to address these limitations, here we propose PALMER, a constrained latent block model that allows to identify indirect relationships among genes based on the biomedical literature mining data. By automatically associating relevant Gene Ontology terms, PALMER facilitates biological interpretation of novel findings without laborious downstream analyses. PALMER also allows researchers to utilize prior biological knowledge about known gene-pathway relationships to guide identification of gene-gene associations. We evaluated PALMER with simulation studies and applications to studies of pathway-modulating genes relevant to cancer signaling pathways, while utilizing biological pathway annotations available in the KEGG database as prior knowledge.

conclusionsWe showed that PALMER outperforms traditional latent block models and it provides reliable identification of novel gene-gene associations by utilizing prior biological knowledge, especially when signals are weak in the biomedical literature mining dataset. We believe that PALMER and its relevant user-friendly software will be powerful tools that can be used to improve existing pathway annotations and identify novel pathway-modulating genes.

Indexed as

AlgorithmsData MiningModels, TheoreticalMolecular Sequence AnnotationPublicationsComputer SimulationGene OntologyGene Regulatory NetworksHumansMultigene FamilySystems BiologyBiomedical literature miningClusteringPathwaySystems biology

Identifiers

PMID33008309
PMCPMC7532116

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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.