Abstract
Global spectrum of CNVs is required to catalog variations to provide a high-resolution on the dynamics of genome-organization and human migration. In this study, we performed genome-wide genotyping using high-resolution arrays and identified 44,109 CNVs from 1,715 genomes across 12 populations. The study unraveled the force of independent evolutionary dynamics on genome-organizational plasticity across populations. We demonstrated the use of CNV tool to study human migration and identified a second major settlement establishing new migration routes in addition to existing ones.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Alleles
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Chromosome Breakpoints
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Chromosome Deletion
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Chromosome Duplication
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Computational Biology / methods
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DNA Copy Number Variations*
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Evolution, Molecular
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Gene Frequency
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Genetics, Population*
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Genome, Human*
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Genome-Wide Association Study
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Genomics*
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Human Migration*
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Humans
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Phylogeny
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Polymorphism, Single Nucleotide
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Reproducibility of Results
Associated data
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figshare/10.6084/M9.FIGSHARE.1320382
Grants and funding
The work was supported by Department of Science and Technology-Health Science, grant number SR/SO/HS-103/2007, funding website -
http://www.dst.gov.in/. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.