Evidence map›Paper›PMID 30846778›Full record

ArticleScientific reports2019

The genetic legacy of continental scale admixture in Indian Austroasiatic speakers.

Kai Tätte, Luca Pagani, Ajai K Pathak, Sulev Kõks, Binh Ho Duy, Xuan Dung Ho, Gazi Nurun Nahar Sultana, Mohd Istiaq Sharif, Md Asaduzzaman, Doron M Behar and 5 more

Erratum issuedOpen 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. An erratum has been issued. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

22 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Genetic Association ofFrontiers in genetics · 2020
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 6 institutions in 8 countries.

Kai TätteDepartment of Evolutionary Biology, Institute of Cell and Molecular Biology, University of Tartu, Tartu, 51010, Estonia. kai.tatte@gmail.com.
Luca PaganiEstonian Biocentre, Institute of Genomics, University of Tartu, Tartu, 51010, Estonia.
Ajai K PathakDepartment of Evolutionary Biology, Institute of Cell and Molecular Biology, University of Tartu, Tartu, 51010, Estonia.
Sulev KõksCentre for Comparative Genomics, Murdoch University, Murdoch, 6150, Australia.
Binh Ho DuyDepartment of Orthopedic and Traumatology, Hue University of Medicine and Pharmacy, Hue University, 06 Ngo Quyen street, Vinh Ninh ward, Hue, Vietnam.
Xuan Dung HoDepartment of Oncology, Hue University of Medicine and Pharmacy, Hue University, 06 Ngo Quyen street, Vinh Ninh ward, Hue, Vietnam.
Gazi Nurun Nahar SultanaCentre for Advanced Research in Sciences (CARS), DNA Sequencing Research Laboratory, University of Dhaka, Dhaka, 1000, Bangladesh.ORCID 0000-0003-4573-7244
Mohd Istiaq SharifCentre for Advanced Research in Sciences (CARS), DNA Sequencing Research Laboratory, University of Dhaka, Dhaka, 1000, Bangladesh.
Md AsaduzzamanCentre for Advanced Research in Sciences (CARS), DNA Sequencing Research Laboratory, University of Dhaka, Dhaka, 1000, Bangladesh.
Doron M BeharEstonian Biocentre, Institute of Genomics, University of Tartu, Tartu, 51010, Estonia.
Yarin HadidThe Genomic Laboratory, The Simon Winter Institute for Human Genetics, The Bnai-Zion Medical Center, 7 Golomb St., Haifa, 31048, Israel.
Richard VillemsDepartment of Evolutionary Biology, Institute of Cell and Molecular Biology, University of Tartu, Tartu, 51010, Estonia.
Gyaneshwer ChaubeyEstonian Biocentre, Institute of Genomics, University of Tartu, Tartu, 51010, Estonia.
Toomas KivisildEstonian Biocentre, Institute of Genomics, University of Tartu, Tartu, 51010, Estonia.
Mait MetspaluEstonian Biocentre, Institute of Genomics, University of Tartu, Tartu, 51010, Estonia. maitb@ut.ee.
Estonian Biocentre · EEUniversity of Dhaka · BDHue University · VNBnai Zion Medical Center · ILMurdoch University · AUUniversity of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Surrounded by speakers of Indo-European, Dravidian and Tibeto-Burman languages, around 11 million Munda (a branch of Austroasiatic language family) speakers live in the densely populated and genetically diverse South Asia. Their genetic makeup holds components characteristic of South Asians as well as Southeast Asians. The admixture time between these components has been previously estimated on the basis of archaeology, linguistics and uniparental markers. Using genome-wide genotype data of 102 Munda speakers and contextual data from South and Southeast Asia, we retrieved admixture dates between 2000-3800 years ago for different populations of Munda. The best modern proxies for the source populations for the admixture with proportions 0.29/0.71 are Lao people from Laos and Dravidian speakers from Kerala in India. The South Asian population(s), with whom the incoming Southeast Asians intermixed, had a smaller proportion of West Eurasian genetic component than contemporary proxies. Somewhat surprisingly Malaysian Peninsular tribes rather than the geographically closer Austroasiatic languages speakers like Vietnamese and Cambodians show highest sharing of IBD segments with the Munda. In addition, we affirmed that the grouping of the Munda speakers into North and South Munda based on linguistics is in concordance with genome-wide data.

Indexed as

Genetics, PopulationGenetic VariationHaplotypesLanguageAsia, SoutheasternDatabases, GeneticDNA, MitochondrialEthnicityGene FrequencyHumansIndiaPhylogenyDNA, Mitochondrial

Identifiers

PMID30846778
PMCPMC6405872
OpenAlexW2953010927

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.