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

Author:

Oleksyk Taras K12ORCID,Wolfsberger Walter W2ORCID,Schubelka Khrystyna2,Mangul Serghei3ORCID,O'Brien Stephen J4ORCID

Affiliation:

1. Uzhhorod National University , Uzhhorod, 88000, Ukraine

2. Oakland University , Department of Biological Sciences, Rochester, 48309 MI 48309-4479, USA

3. University of Southern California , USC School of Pharmacy, Los Angeles, CA 90089, USA

4. Nova Southeastern University , Halmos College of Natural Sciences and Oceanography, Fort Lauderdale, FL 33314, USA

Abstract

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.

Funder

European Neighbourhood Instrument

Publisher

Oxford University Press (OUP)

Subject

Computer Science Applications,Health Informatics

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