Abstract
To facilitate the practical application of highly efficient semiautomated methods for general application in genomic analyses, we have developed a fluorescence-based microsatellite marker resource. Ninety highly polymorphic microsatellite markers were combined to provide a rapid, accurate, and highly efficient initial genome-wide screening system. These markers are spaced on average every 33 cM, with a mean heterozygosity of 81% (range 65-94%), covering 22 autosomes and the X and Y chromosomes. Less than 10% of the genome lies beyond 20 cM of the nearest marker. Since this genomic analysis system is fully compatible with automated fragment analyzers using simultaneous four-color fluorescence-based detection systems, the 5 groups of 18 markers can be detected concurrently. This multiplex detection provides a throughput of 1944 genotypes daily per instrument. This system will be highly beneficial in a number of clinical and research applications including linkage, cancer genetics, forensics, and cytogenetics. © 1994 Academic Press. All rights reserved.
Cite
CITATION STYLE
Levitt, R. C., Kiser, M. B., Dragwa, C., Jedlicka, A. E., Xu, J., Meyers, D. A., & Hudson, J. R. (1994). Fluorescence-based resource for semiautomated genomic analyses using microsatellite markers. Genomics, 24(2), 361–365. https://doi.org/10.1006/geno.1994.1628
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