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Estimating genomic distance from DNA sequence location in cell nuclei by a random walk model.
van den Engh, G; Sachs, R; Trask, B J.
Affiliation
  • van den Engh G; Human Genome Center, Lawrence Livermore National Laboratory, Livermore, CA 94550.
Science ; 257(5075): 1410-2, 1992 Sep 04.
Article in En | MEDLINE | ID: mdl-1388286
ABSTRACT
The folding of chromatin in interphase cell nuclei was studied by fluorescent in situ sequences chromatin according to a random walk model. This model provides the basis for calculating the spacing of sequences along the linear DNA molecule from interphase distance measurements. An interphase mapping strategy based on this model was tested with 13 probes from a 4-megabase pair (Mbp) region of chromosome 4 containing the Huntington disease locus. The results confirmed the locations of the probes and showed that the remaining gap in the published maps of this region is negligible in size. Interphase distance measurements should facilitate construction of chromosome maps with an average marker density of one per 100 kbp, approximately ten times greater than that achieved by hybridization to metaphase chromosome. achieved by hybridization to metaphase chromosomes.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: DNA / Chromatin / Cell Nucleus / Interphase Type of study: Clinical_trials Limits: Humans Language: En Journal: Science Year: 1992 Type: Article
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: DNA / Chromatin / Cell Nucleus / Interphase Type of study: Clinical_trials Limits: Humans Language: En Journal: Science Year: 1992 Type: Article