Evidence map›Paper›PMID 31739607›Full record

ArticleGenes2019

HisCoM-PAGE: Hierarchical Structural Component Models for Pathway Analysis of Gene Expression Data.

Lydia Mok, Yongkang Kim, Sungyoung Lee, Sungkyoung Choi, Seungyeoun Lee, Jin-Young Jang, Taesung Park

Abstract read
In one paragraph

Article in Genes, 2019. 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.

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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.

Lydia MokInterdisciplinary Program in Bioinformatics, Seoul National University, Seoul 08826, Korea.
Yongkang KimDepartment of Statistics, Seoul National University, Seoul 08826, Korea.
Sungyoung LeeCenter for Precision Medicine, Seoul National University Hospital, Seoul 03080, Korea.
Sungkyoung ChoiDepartment of Applied Mathematics, Hanyang University (ERICA), Ansan 15588, Korea.
Seungyeoun LeeDepartment of Mathematics and Statistics, Sejong University, Seoul 05006, Korea.
Jin-Young JangDepartment of Surgery, Seoul National University College of Medicine, Seoul 03080, Korea.
Taesung ParkInterdisciplinary Program in Bioinformatics, Seoul National University, Seoul 08826, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although there have been several analyses for identifying cancer-associated pathways, based on gene expression data, most of these are based on single pathway analyses, and thus do not consider correlations between pathways. In this paper, we propose a hierarchical structural component model for pathway analysis of gene expression data (HisCoM-PAGE), which accounts for the hierarchical structure of genes and pathways, as well as the correlations among pathways. Specifically, HisCoM-PAGE focuses on the survival phenotype and identifies its associated pathways. Moreover, its application to real biological data analysis of pancreatic cancer data demonstrated that HisCoM-PAGE could successfully identify pathways associated with pancreatic cancer prognosis. Simulation studies comparing the performance of HisCoM-PAGE with other competing methods such as Gene Set Enrichment Analysis (GSEA), Global Test, and Wald-type Test showed HisCoM-PAGE to have the highest power to detect causal pathways in most simulation scenarios.

Indexed as

Data AnalysisGene Expression Regulation, NeoplasticModels, GeneticAgedAlgorithmsCarcinoma, Pancreatic DuctalComputer SimulationDatabases, GeneticDatasets as TopicFeasibility StudiesFemaleGene Regulatory NetworksHumansMaleMiddle AgedOligonucleotide Array Sequence AnalysisHierarchical structured component modelPathway analysisSurvival phenotype

Identifiers

PMID31739607
PMCPMC6896173

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Registered trials

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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.