Evidence map›Paper›PMID 29379686›Full record

ArticlePeerJ2018

Genomic signal processing for DNA sequence clustering.

Gerardo Mendizabal-Ruiz, Israel Román-Godínez, Sulema Torres-Ramos, Ricardo A Salido-Ruiz, Hugo Vélez-Pérez, J Alejandro Morales

Abstract read
In one paragraph

Article in PeerJ, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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  4. An Information-Entropy Position-WeightedFrontiers in genetics · 2021
    Article
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  6. Review
  7. Article
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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

6 authors.

Gerardo Mendizabal-RuizDepartamento de Ciencias Computacionales, Universidad de Guadalajara, Guadalajara, Mexico.
Israel Román-GodínezDepartamento de Ciencias Computacionales, Universidad de Guadalajara, Guadalajara, Mexico.
Sulema Torres-RamosDepartamento de Ciencias Computacionales, Universidad de Guadalajara, Guadalajara, Mexico.
Ricardo A Salido-RuizDepartamento de Ciencias Computacionales, Universidad de Guadalajara, Guadalajara, Mexico.
Hugo Vélez-PérezDepartamento de Ciencias Computacionales, Universidad de Guadalajara, Guadalajara, Mexico.
J Alejandro MoralesDepartamento de Ciencias Computacionales, Universidad de Guadalajara, Guadalajara, Mexico.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genomic signal processing (GSP) methods which convert DNA data to numerical values have recently been proposed, which would offer the opportunity of employing existing digital signal processing methods for genomic data. One of the most used methods for exploring data is cluster analysis which refers to the unsupervised classification of patterns in data. In this paper, we propose a novel approach for performing cluster analysis of DNA sequences that is based on the use of GSP methods and the K-means algorithm. We also propose a visualization method that facilitates the easy inspection and analysis of the results and possible hidden behaviors. Our results support the feasibility of employing the proposed method to find and easily visualize interesting features of sets of DNA data.

Indexed as

COX1DNAGenomic signal processingK-meansSequence clustering

Identifiers

PMID29379686
PMCPMC5786891

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.