Evidence map›Paper›PMID 25633916›Full record

ArticleScientific reports2015

Highlighting nonlinear patterns in population genetics datasets.

Gregorio Alanis-Lobato, Carlo Vittorio Cannistraci, Anders Eriksson, Andrea Manica, Timothy Ravasi

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Simplicity within biological complexity.Bioinformatics advances · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Geometric characterisation of disease modules.Applied network science · 2018
    Article
  18. Clustering: how much bias do we need?Philosophical transactions. Series A, Mathematical, physical, and engineering sciences · 2017
    Article
  19. Article
  20. Article
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

5 authors.

Gregorio Alanis-Lobato1] Integrative Systems Biology Laboratory, Biological and Environmental Sciences and Engineering Division, Computer, Electrical and Mathematical Sciences and Engineering Division, Computational Bioscience Research Center, King Abdullah University of Science and Technology (KAUST), Ibn Al Haytham Bldg. 2, Level 4, Thuwal 23955-6900, Kingdom of Saudi Arabia [2] Division of Medical Genetics, Department of Medicine, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093 USA.
Carlo Vittorio CannistraciBiomedical Cybernetics Group, Biotechnology Center (BIOTEC), Technische Universität Dresden, Tatzberg 47/49, 01307 Dresden, Germany.
Anders Eriksson1] Integrative Systems Biology Laboratory, Biological and Environmental Sciences and Engineering Division, Computer, Electrical and Mathematical Sciences and Engineering Division, Computational Bioscience Research Center, King Abdullah University of Science and Technology (KAUST), Ibn Al Haytham Bldg. 2, Level 4, Thuwal 23955-6900, Kingdom of Saudi Arabia [2] Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, England.
Andrea ManicaDepartment of Zoology, University of Cambridge, Cambridge CB2 3EJ, England.
Timothy Ravasi1] Integrative Systems Biology Laboratory, Biological and Environmental Sciences and Engineering Division, Computer, Electrical and Mathematical Sciences and Engineering Division, Computational Bioscience Research Center, King Abdullah University of Science and Technology (KAUST), Ibn Al Haytham Bldg. 2, Level 4, Thuwal 23955-6900, Kingdom of Saudi Arabia [2] Division of Medical Genetics, Department of Medicine, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093 USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Detecting structure in population genetics and case-control studies is important, as it exposes phenomena such as ecoclines, admixture and stratification. Principal Component Analysis (PCA) is a linear dimension-reduction technique commonly used for this purpose, but it struggles to reveal complex, nonlinear data patterns. In this paper we introduce non-centred Minimum Curvilinear Embedding (ncMCE), a nonlinear method to overcome this problem. Our analyses show that ncMCE can separate individuals into ethnic groups in cases in which PCA fails to reveal any clear structure. This increased discrimination power arises from ncMCE's ability to better capture the phylogenetic signal in the samples, whereas PCA better reflects their geographic relation. We also demonstrate how ncMCE can discover interesting patterns, even when the data has been poorly pre-processed. The juxtaposition of PCA and ncMCE visualisations provides a new standard of analysis with utility for discovering and validating significant linear/nonlinear complementary patterns in genetic data.

Indexed as

Databases, GeneticGenetics, PopulationNonlinear DynamicsAlgorithmsAsian PeopleGenotypeHumansPrincipal Component AnalysisStatistics, Nonparametric

Identifiers

PMID25633916
PMCPMC4311249

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.