Evidence map›Paper›PMID 34148879›Full record

ArticleJournal of biosciences2021

PD_BiBIM: Biclustering-based biomarker identification in ESCC microarray data.

Pallabi Patowary, Dhruba K Bhattacharyya

Abstract read
PubMed
In one paragraph

Article in Journal of biosciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Pallabi PatowaryDepartment of Computer Science and Engineering, Tezpur University, Tezpur, Assam, India.
Dhruba K Bhattacharyya

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To promote diligent analysis of the progression of a disease, it is important to identify interesting biomarkers for the disease. Biclustering has already been established as an effective technique to help identify such biomarkers of high biological significance. Although in the recent past, a good number of biclustering techniques have been introduced, most of them fail to perform consistently across multiple domains or datasets. To choose a single biclustering technique that can help the accomplishment of such a critical task for multiple diseases with high precision is extremely difficult. Hence, in this study, we considered several biclustering techniques and accepted those techniques and their results which are found significant from enrichment perspective for subsequent analysis. Based on biclustering results, we constructed biological networks and carried out a topological, pathway and causal analysis on the modules extracted from the networks. Our multiobjective study enabled us to identify several biomarkers for esophageal squamous cell carcinoma (ESCC) such as IFNGR1, CLIC1, CDK4, and COPS5, after applying a ranking scheme.

Indexed as

Biomarkers, TumorChloride ChannelsCluster AnalysisComputational BiologyCOP9 Signalosome ComplexCyclin-Dependent Kinase 4Datasets as TopicEsophageal NeoplasmsEsophageal Squamous Cell CarcinomaGene Expression ProfilingGene Expression Regulation, NeoplasticGene OntologyGene Regulatory NetworksHumansInterferon gamma ReceptorIntracellular Signaling Peptides and ProteinsBiomarkers, TumorCDK4 protein, humanChloride ChannelsCLIC1 protein, humanCOP9 Signalosome ComplexCOPS5 protein, humanCyclin-Dependent Kinase 4Interferon gamma ReceptorIntracellular Signaling Peptides and ProteinsNeoplasm ProteinsPeptide HydrolasesReceptors, Interferon

Identifiers

PMID34148879

What OpenQuestion holds

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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.