Evidence map›Paper›PMID 36085557›Full record

ArticleGigaScience2022

The Pioneer Advantage: Filling the blank spots on the map of genome diversity in Europe.

Taras K Oleksyk, Walter W Wolfsberger, Khrystyna Schubelka, Serghei Mangul, Stephen J O'Brien

Abstract read
In one paragraph

Article in GigaScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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  7. WGS Data Collections: How Do Genomic Databases Transform Medicine?International journal of molecular sciences · 2023
    Review
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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

5 authors.

Taras K OleksykUzhhorod National University, Uzhhorod, 88000, Ukraine.ORCID 0000-0002-8148-3918
Walter W WolfsbergerOakland University, Department of Biological Sciences, Rochester, 48309 MI 48309-4479, USA.ORCID 0000-0003-0980-645X
Khrystyna SchubelkaOakland University, Department of Biological Sciences, Rochester, 48309 MI 48309-4479, USA.
Serghei MangulUniversity of Southern California, USC School of Pharmacy, Los Angeles, CA 90089, USA.ORCID 0000-0003-4770-3443
Stephen J O'BrienNova Southeastern University, Halmos College of Natural Sciences and Oceanography, Fort Lauderdale, FL 33314, USA.ORCID 0000-0001-7353-8301

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Documenting genome diversity is important for the local biomedical communities and instrumental in developing precision and personalized medicine. Currently, tens of thousands of whole-genome sequences from Europe are publicly available, but most of these represent populations of developed countries of Europe. The uneven distribution of the available data is further impaired by the lack of data sharing. Recent whole-genome studies in Eastern Europe, one in Ukraine and one in Russia, demonstrated that local genome diversity and population structure from Eastern Europe historically had not been fully represented. An unexpected wealth of genomic variation uncovered in these studies was not so much a consequence of high variation within their population, but rather due to the "pioneer advantage." We discovered more variants because we were the first to prospect in the Eastern European genome pool. This simple comparison underscores the importance of removing the remaining geographic genome deserts from the rest of the world map of the human genome diversity.

Indexed as

Genome, HumanGenomicsEuropeHumansInformation DisseminationPrecision MedicineEuropegenome desertsgenome diversitygenome projectgenomesgenotypingRussiaUkrainevariantswhole-genome sequencing

Identifiers

PMID36085557
PMCPMC9463063

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.