Evidence map›Paper›PMID 33554061›Full record

ArticleiScience2021

Spatial constrains and information content of sub-genomic regions of the human genome.

Leonidas P Karakatsanis, Evgenios G Pavlos, George Tsoulouhas, Georgios L Stamokostas, Timothy Mosbruger, Jamie L Duke, George P Pavlos, Dimitri S Monos

Abstract read
In one paragraph

Article in iScience, 2021. 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. Review
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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

8 authors.

Leonidas P KarakatsanisDepartment of Environmental Engineering, Complexity Research Team (CRT), Democritus University of Thrace, 67100 Xanthi, Greece.
Evgenios G PavlosDepartment of Environmental Engineering, Complexity Research Team (CRT), Democritus University of Thrace, 67100 Xanthi, Greece.
George TsoulouhasDepartment of Environmental Engineering, Complexity Research Team (CRT), Democritus University of Thrace, 67100 Xanthi, Greece.
Georgios L StamokostasDepartment of Environmental Engineering, Complexity Research Team (CRT), Democritus University of Thrace, 67100 Xanthi, Greece.
Timothy MosbrugerDepartment of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Jamie L DukeDepartment of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
George P PavlosDepartment of Environmental Engineering, Complexity Research Team (CRT), Democritus University of Thrace, 67100 Xanthi, Greece.
Dimitri S MonosDepartment of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia and Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complexity metrics and machine learning (ML) models have been utilized to analyze the lengths of segmental genomic entities of DNA sequences (exonic, intronic, intergenic, repeat, unique) with the purpose to ask questions regarding the segmental organization of the human genome within the size distribution of these sequences. For this we developed an integrated methodology that is based upon the reconstructed phase space theorem, the non-extensive statistical theory of Tsallis, ML techniques, and a technical index, integrating the generated information, which we introduce and named complexity factor (COFA). Our analysis revealed that the size distribution of the genomic regions within chromosomes are not random but follow patterns with characteristic features that have been seen through its complexity character, and it is part of the dynamics of the whole genome. Finally, this picture of dynamics in DNA is recognized using ML tools for clustering, classification, and prediction with high accuracy.

Indexed as

Biocomputational MethodBioinformaticsBiological SciencesGenomic AnalysisGenomicsStatistical PhysicsTechniques in Genetics

Identifiers

PMID33554061
PMCPMC7843455

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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.