A combined linkage-physical map of the human genome
- PMID: 15486828
- PMCID: PMC1182151
- DOI: 10.1086/426405
A combined linkage-physical map of the human genome
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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References
Electronic-Database Information
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- Authors' Web site, http://compgen.rutgers.edu/maps/ (for Rutgers Linkage-Physical Maps)
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- Center for Medical Genetics, Marshfield Clinic, http://research.marshfieldclinic.org/genetics/ (for the Marshfield genetic maps)
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- CEPH Genotype Database, http://www.cephb.fr/cephdb/
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- dbSNP Home Page, http://www.ncbi.nlm.nih.gov/SNP/
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- eGenome, http://genome.chop.edu/
References
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- Bahlo M, Xing L, Wilkinson CR (2004) HumanMSD and MouseMSD: generating genetic maps for human and murine microsatellite markers. Bioinformatics. http://bioinformatics.oupjournals.org/cgi/reprint/bth375v1 (electronically published June 24, 2004; accessed October 12, 2004) - PubMed
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- Dausset J, Cann H, Cohen D, Lathrop M, Lalouel J-M, White R (1990) Centre d’Etude du Polymorphisme Humain (CEPH): collaborative genetic mapping of the human genome. Genomics 6:575–577 - PubMed
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