4.2 Article

The polymorphism architecture of mouse genetic resources elucidated using genome-wide resequencing data: implications for QTL discovery and systems genetics

Journal

MAMMALIAN GENOME
Volume 18, Issue 6-7, Pages 473-481

Publisher

SPRINGER
DOI: 10.1007/s00335-007-9045-1

Keywords

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Funding

  1. NCI NIH HHS [5P30 CA016086, P30 CA016086, U01 CA105417, 1U01 CA105417] Funding Source: Medline
  2. NIDDK NIH HHS [P30 DK034987, 5P30 DK034987] Funding Source: Medline
  3. NIEHS NIH HHS [2P30 ES010126, P30 ES010126] Funding Source: Medline
  4. NIGMS NIH HHS [1P50 GM076468, P50 GM076468] Funding Source: Medline

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Mouse genetic resources include inbred strains, recombinant inbred lines, chromosome substitution strains, heterogeneous stocks, and the Collaborative Cross (CC). These resources were generated through various breeding designs that potentially produce different genetic architectures. including the level of diversity represented, the C spatial distribution of the variation, and the allele frequencies within the resource. By combining sequencing data for 16 inbred strains and the recorded history of related strains, the architecture of genetic variation in mouse resources was determined. The most commonly used resources harbor only a fraction of the genetic diversity of Mus inusculus, which is not uniformly distributed thus resulting in many blind spots. Only resources that include wild-derived inbred strains from subspecies other than M. m. domesticits have no blind spots and a uniform distribution of the variation. Unlike other resources that are primarily suited for gene discovery, the CC is the only resource that can support genome-wide network analysis, which is the foundation of systems genetics. The CC captures significantly more genetic diversity with no blind spots and has a more uniform distribution of the variation than all other resources. Furthermore, the distribution of allele frequencies in the CC resembles that seen in natural populations like humans in which many variants are found at low frequencies and only a minority of variants are common. We conclude that the CC represents a dramatic improvement over existing genetic resources for mammalian systems biology applications.

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