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The origins and impact of primate segmental duplications

Journal

TRENDS IN GENETICS
Volume 25, Issue 10, Pages 443-454

Publisher

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tig.2009.08.002

Keywords

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Funding

  1. NIH [GM058815, HG002385]
  2. Marie Curie fellowship
  3. NATIONAL HUMAN GENOME RESEARCH INSTITUTE [R01HG002385] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM058815] Funding Source: NIH RePORTER

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Duplicated sequences are substrates for the emergence of new genes and are an important source of genetic instability associated with rare and common diseases. Analyses of primate genomes have shown an increase in the proportion of interspersed segmental duplications (SDs) within the genomes of humans and great apes. This contrasts with other mammalian genomes that seem to have their recently duplicated sequences organized in a tandem configuration. In this review, we focus on the mechanistic origin and impact of this difference with respect to evolution, genetic diversity and primate phenotype. Although many genomes will be sequenced in the future, resolution of this aspect of genomic architecture still requires high quality sequences and detailed analyses.

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