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. 2004 Dec;75(6):1143-8.
doi: 10.1086/426405. Epub 2004 Oct 14.

A combined linkage-physical map of the human genome

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A combined linkage-physical map of the human genome

X Kong et al. Am J Hum Genet. 2004 Dec.

Erratum in

  • Am J Hum Genet. 2005 Feb;76(2):373

Abstract

We have constructed de novo a high-resolution genetic map that includes the largest set, to our knowledge, of polymorphic markers (N=14,759) for which genotype data are publicly available; that combines genotype data from both the Centre d'Etude du Polymorphisme Humain (CEPH) and deCODE pedigrees; that incorporates single-nucleotide polymorphisms; and that also incorporates sequence-based positional information. The position of all markers on our map is corroborated by both genomic sequence and recombination-based data. This specific combination of features maximizes marker inclusion, coverage, and resolution, making this map uniquely suitable as a comprehensive resource for determining genetic map information (order and distances) for any large set of polymorphic markers.

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Figures

Figure  1
Figure 1
Frequency distribution of the number of informative meioses per marker.
Figure  2
Figure 2
Comparison of map distances on our map of chromosome 3, using only the genotype data from the CEPH pedigrees (dotted line) versus using only the genotype data from the deCODE pedigrees (solid line). Similar graphs for all chromosomes can be viewed on the authors' Web site.

References

Electronic-Database Information

    1. Authors' Web site, http://compgen.rutgers.edu/maps/ (for Rutgers Linkage-Physical Maps)
    1. Center for Medical Genetics, Marshfield Clinic, http://research.marshfieldclinic.org/genetics/ (for the Marshfield genetic maps)
    1. CEPH Genotype Database, http://www.cephb.fr/cephdb/
    1. dbSNP Home Page, http://www.ncbi.nlm.nih.gov/SNP/
    1. eGenome, http://genome.chop.edu/

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