Evidence map›Paper›PMID 31240260›Full record

ArticleCommunications biology2019

GECKO is a genetic algorithm to classify and explore high throughput sequencing data.

Aubin Thomas, Sylvain Barriere, Lucile Broseus, Julie Brooke, Claudio Lorenzi, Jean-Philippe Villemin, Gregory Beurier, Robert Sabatier, Christelle Reynes, Alban Mancheron and 1 more

Abstract read
In one paragraph

Article in Communications biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. A survey of k-mer methods and applications in bioinformatics.Computational and structural biotechnology journal · 2024
    Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. 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

11 authors.

Aubin Thomas *1Institute of Human Genetics, CNRS UPR1142, Machine learning and gene regulation, University of Montpellier, Montpellier, France.
Sylvain Barriere *1Institute of Human Genetics, CNRS UPR1142, Machine learning and gene regulation, University of Montpellier, Montpellier, France.
Lucile Broseus1Institute of Human Genetics, CNRS UPR1142, Machine learning and gene regulation, University of Montpellier, Montpellier, France.
Julie Brooke1Institute of Human Genetics, CNRS UPR1142, Machine learning and gene regulation, University of Montpellier, Montpellier, France.
Claudio Lorenzi1Institute of Human Genetics, CNRS UPR1142, Machine learning and gene regulation, University of Montpellier, Montpellier, France.
Jean-Philippe Villemin1Institute of Human Genetics, CNRS UPR1142, Machine learning and gene regulation, University of Montpellier, Montpellier, France.
Gregory Beurier2AGAP, Univ Montpellier, CIRAD, INRA, Montpellier SupAgro, Montpellier, France.ORCID 0000-0002-5621-7079
Robert Sabatier3IGF, Centre National de la Recherche Scientifique, INSERM U1191, University of Montpellier, Montpellier, France.
Christelle Reynes3IGF, Centre National de la Recherche Scientifique, INSERM U1191, University of Montpellier, Montpellier, France.
Alban Mancheron4LIRMM, Université de Montpellier, CNRS, UMR5506, Montpellier, France.
William Ritchie1Institute of Human Genetics, CNRS UPR1142, Machine learning and gene regulation, University of Montpellier, Montpellier, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Comparative analysis of high throughput sequencing data between multiple conditions often involves mapping of sequencing reads to a reference and downstream bioinformatics analyses. Both of these steps may introduce heavy bias and potential data loss. This is especially true in studies where patient transcriptomes or genomes may vary from their references, such as in cancer. Here we describe a novel approach and associated software that makes use of advances in genetic algorithms and feature selection to comprehensively explore massive volumes of sequencing data to classify and discover new sequences of interest without a mapping step and without intensive use of specialized bioinformatics pipelines. We demonstrate that our approach called GECKO for GEnetic Classification using

Indexed as

AlgorithmsBlood CellsBreast NeoplasmsComputational BiologyDNA MethylationHigh-Throughput Nucleotide SequencingHumansMicroRNAsMutationRNA, MessengerSoftwareMicroRNAsRNA, MessengerMachine learningPredictive medicine

Identifiers

PMID31240260
PMCPMC6586863

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.