Abstract
Twenty-two human chromosome 3 derived and partially sequencedNotl linking clones were mapped using two somatic cell hybrid panels. Somatic cell hybrid mapping was performed by Southern hybridization and/or by polymerase chain reaction (PCR), using 300–500 bp CpG-rich sequences surroundingNotl sites. Thus, 22 newNotl site-tagged (sequence tagged sites) STSs were created, distributed over the entire human chromosome 3. The majority of these linking clones tag known or unknown expressed sequences (genes). Together with other physical and genetic mapping methods, localization ofNotl linking clones facilitates the construction of a long-range physical map and, at the same time, a transcriptional map of human chromosome 3.
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accepted for publication by G. R. Sutherland
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Allikmets, R., Kashuba, V.I., Huebner, K. et al. Mapping of 22Notl linking clones on human chromosome 3 by polymerase chain reaction and somatic cell hybrid panels. Chromosome Res 4, 33–37 (1996). https://doi.org/10.1007/BF02254942
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DOI: https://doi.org/10.1007/BF02254942