Evidence map›Paper›PMID 27764138›Full record

ArticlePloS one2016

IGSA: Individual Gene Sets Analysis, including Enrichment and Clustering.

Lingxiang Wu, Xiujie Chen, Denan Zhang, Wubing Zhang, Lei Liu, Hongzhe Ma, Jingbo Yang, Hongbo Xie, Bo Liu, Qing Jin

Abstract readComparative Study
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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  5. Article
  6. Integrating RNA sequencing into neuro-oncology practice.Translational research : the journal of laboratory and clinical medicine · 2017
    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

10 authors.

Lingxiang WuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Xiujie ChenCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Denan ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Wubing ZhangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Lei LiuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Hongzhe MaCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Jingbo YangCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Hongbo XieCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Bo LiuCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.
Qing JinCollege of Bioinformatics Science and Technology, Harbin Medical University, Harbin, Heilongjiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Analysis of gene sets has been widely applied in various high-throughput biological studies. One weakness in the traditional methods is that they neglect the heterogeneity of genes expressions in samples which may lead to the omission of some specific and important gene sets. It is also difficult for them to reflect the severities of disease and provide expression profiles of gene sets for individuals. We developed an application software called IGSA that leverages a powerful analytical capacity in gene sets enrichment and samples clustering. IGSA calculates gene sets expression scores for each sample and takes an accumulating clustering strategy to let the samples gather into the set according to the progress of disease from mild to severe. We focus on gastric, pancreatic and ovarian cancer data sets for the performance of IGSA. We also compared the results of IGSA in KEGG pathways enrichment with David, GSEA, SPIA, ssGSEA and analyzed the results of IGSA clustering and different similarity measurement methods. Notably, IGSA is proved to be more sensitive and specific in finding significant pathways, and can indicate related changes in pathways with the severity of disease. In addition, IGSA provides with significant gene sets profile for each sample.

Indexed as

Gene Regulatory NetworksAlgorithmsCluster AnalysisComputational BiologyDatabases, GeneticFemaleGene Expression Regulation, NeoplasticGenetic Predisposition to DiseaseHumansOvarian NeoplasmsPancreatic NeoplasmsSoftwareStomach Neoplasms

Identifiers

PMID27764138
PMCPMC5072653

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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.