Evidence map›Paper›PMID 30765821›Full record

ArticleScientific reports2019

Whole Genome Sequence, Variant Discovery and Annotation in Mapuche-Huilliche Native South Americans.

Elena A Vidal, Tomás C Moyano, Bernabé I Bustos, Eduardo Pérez-Palma, Carol Moraga, Eleodoro Riveras, Alejandro Montecinos, Lorena Azócar, Daniela C Soto, Mabel Vidal and 21 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 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
0.9field-weighted citation impact, top 28% of its field
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, 20 citations in OpenAlex.

  1. Egypt Genome: Towards an African new genomic era.Journal of advanced research · 2025
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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

31 authors at 6 institutions in 3 countries.

Elena A VidalFONDAP Center for Genome Regulation, Santiago, Chile.
Tomás C MoyanoFONDAP Center for Genome Regulation, Santiago, Chile.
Bernabé I BustosFONDAP Center for Genome Regulation, Santiago, Chile.
Eduardo Pérez-PalmaFONDAP Center for Genome Regulation, Santiago, Chile.
Carol MoragaFONDAP Center for Genome Regulation, Santiago, Chile.
Eleodoro RiverasFONDAP Center for Genome Regulation, Santiago, Chile.
Alejandro MontecinosFONDAP Center for Genome Regulation, Santiago, Chile.
Lorena AzócarFONDAP Center for Genome Regulation, Santiago, Chile.
Daniela C SotoFONDAP Center for Genome Regulation, Santiago, Chile.
Mabel VidalFONDAP Center for Genome Regulation, Santiago, Chile.
Alex Di GenovaFONDAP Center for Genome Regulation, Santiago, Chile.
Klaus PuschelDepartamento de Medicina Familiar, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
Peter NürnbergCologne Center for Genomics (CCG), University of Cologne, Cologne, Germany.
Stephan BuchMedical Department I, University Hospital Dresden, TU Dresden, Germany.
Jochen HampeMedical Department I, University Hospital Dresden, TU Dresden, Germany.ORCID 0000-0002-2421-6127
Miguel L AllendeFONDAP Center for Genome Regulation, Santiago, Chile.ORCID 0000-0002-2783-2152
Verónica CambiazoFONDAP Center for Genome Regulation, Santiago, Chile.
Mauricio GonzálezFONDAP Center for Genome Regulation, Santiago, Chile.
Christian HodarFONDAP Center for Genome Regulation, Santiago, Chile.
Martín MontecinoFONDAP Center for Genome Regulation, Santiago, Chile.
Claudia Muñoz-EspinozaFONDAP Center for Genome Regulation, Santiago, Chile.
Ariel OrellanaFONDAP Center for Genome Regulation, Santiago, Chile.ORCID 0000-0002-9243-808X
Angélica Reyes-JaraFONDAP Center for Genome Regulation, Santiago, Chile.
Dante TravisanyFONDAP Center for Genome Regulation, Santiago, Chile.
Paula VizosoFONDAP Center for Genome Regulation, Santiago, Chile.
Mauricio MoragaInstituto de Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile, Santiago, Chile.
Susana EyheramendyDepartmento de Estadística, Facultad de Matemáticas, Pontificia Universidad Católica de Chile, Santiago, Chile.
Alejandro MaassFONDAP Center for Genome Regulation, Santiago, Chile.
Giancarlo V De FerrariFONDAP Center for Genome Regulation, Santiago, Chile. gdeferrari@unab.cl.ORCID 0000-0003-0932-125X
Juan Francisco MiquelFONDAP Center for Genome Regulation, Santiago, Chile. jfmiquel@med.puc.cl.
Rodrigo A GutiérrezFONDAP Center for Genome Regulation, Santiago, Chile. rgutierrez@bio.puc.cl.ORCID 0000-0002-5961-5005
Pontificia Universidad Católica de Chile · CLUniversity of Chile · CLUniversidad Andrés Bello · CLTechnische Universität Dresden · DEUniversidad Mayor · CLUniversity of Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Whole human genome sequencing initiatives help us understand population history and the basis of genetic diseases. Current data mostly focuses on Old World populations, and the information of the genomic structure of Native Americans, especially those from the Southern Cone is scant. Here we present annotation and variant discovery from high-quality complete genome sequences of a cohort of 11 Mapuche-Huilliche individuals (HUI) from Southern Chile. We found approximately 3.1 × 10

Indexed as

Genetic MarkersGenetics, PopulationGenome, HumanPolymorphism, Single NucleotideAdultAgedAged, 80 and overChileCohort StudiesDNA Copy Number VariationsEthnicityFemaleGenomicsHaplotypesHumansMaleGenetic Markers

Identifiers

PMID30765821
PMCPMC6376018
OpenAlexW2914521544

What Socratic 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 Socratic graph.