Evidence map›Paper›PMID 24498042›Full record

ArticlePloS one2014

Evaluating the X chromosome-specific diversity of Colombian populations using insertion/deletion polymorphisms.

Adriana Ibarra, Tomás Restrepo, Winston Rojas, Adriana Castillo, António Amorim, Beatriz Martínez, German Burgos, Henry Ostos, Karen Álvarez, Mauricio Camacho and 3 more

Abstract readEvaluation Study
In one paragraph

Article in PloS one, 2014. 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. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. X-chromosomal 21-indel marker panel in German and Baltic populations.International journal of legal medicine · 2016
    Article
  9. Article
  10. 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

13 authors.

Adriana IbarraIdentiGEN - Genetic Identification Laboratory and Research Group of Genetic Identification, Institute of Biology, School of Natural and Exact Sciences (FCEN), University of Antioquia, Medellin, Antioquia, Colombia.
Tomás RestrepoIdentiGEN - Genetic Identification Laboratory and Research Group of Genetic Identification, Institute of Biology, School of Natural and Exact Sciences (FCEN), University of Antioquia, Medellin, Antioquia, Colombia.
Winston RojasLaboratory of Molecular Genetics, Institute of Biology, University of Antioquia, Medellin, Antioquia, Colombia.
Adriana CastilloLaboratorio de Genética, Universidad Industrial de Santander (UIS), Bucaramanga, Santander, Colombia.
António AmorimIPATIMUP - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal ; FCUP - Faculty of Sciences of the University of Porto, Porto, Portugal.
Beatriz MartínezMolecular Genetics Laboratory, Institute for Immunological Research, University of Cartagena, Cartagena, Bolivar, Colombia.
German BurgosMolecular Genetics Laboratory, Cruz Vital, Ecuadorian Red Cross, Quito, Ecuador.
Henry OstosGenomic Medicine Laboratory, Health Faculty, Surcolombiana University, Neiva, Huila, Colombia.
Karen ÁlvarezIdentiGEN - Genetic Identification Laboratory and Research Group of Genetic Identification, Institute of Biology, School of Natural and Exact Sciences (FCEN), University of Antioquia, Medellin, Antioquia, Colombia.
Mauricio CamachoInstitute of Legal Medicine and Forensic Sciences, Northeast Regional, Arauca, Colombia.
Zuleyma SuarezClinical Laboratory Olga Zuleima Suárez Molina, Cucuta, Norte de Santander, Colombia.
Rui PereiraIPATIMUP - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal.
Leonor GusmãoIPATIMUP - Institute of Molecular Pathology and Immunology of the University of Porto, Porto, Portugal ; DNA Diagnostic Laboratory (LDD), State University of Rio de Janeiro (UERJ), Rio de Janeiro, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The European and African contribution to the pre-existing Native American background has influenced the complex genetic pool of Colombia. Because colonisation was not homogeneous in this country, current populations are, therefore, expected to have different proportions of Native American, European and African ancestral contributions. The aim of this work was to examine 11 urban admixed populations and a Native American group, called Pastos, for 32 X chromosome indel markers to expand the current knowledge concerning the genetic background of Colombia. The results revealed a highly diverse genetic background comprising all admixed populations, harbouring important X chromosome contributions from all continental source populations. In addition, Colombia is genetically sub-structured, with different proportions of European and African influxes depending on the regions. The samples from the North Pacific and Caribbean coasts have a high African ancestry, showing the highest levels of diversity. The sample from the South Andean region showed the lowest diversity and significantly higher proportion of Native American ancestry than the other samples from the North Pacific and Caribbean coasts, Central-West and Central-East Andean regions, and the Orinoquian region. The results of admixture analysis using X-chromosomal markers suggest that the high proportion of African ancestry in the North Pacific coast was primarily male driven. These men have joined to females with higher Native American and European ancestry (likely resulting from a classic colonial asymmetric mating type: European male x Amerindian female). This high proportion of male-mediated African contributions is atypical of colonial settings, suggesting that the admixture occurred during a period when African people were no longer enslaved. In the remaining regions, the African contribution was primarily female-mediated, whereas the European counterpart was primarily male driven and the Native American ancestry contribution was not gender biased.

Indexed as

Genetic VariationINDEL MutationPolymorphism, GeneticBlack PeopleChromosomes, Human, XColombiaFemaleGene FlowGene FrequencyGenetics, PopulationGenotypeGeographyHumansIndians, South AmericanLinkage DisequilibriumMale

Identifiers

PMID24498042
PMCPMC3909073

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.