R. F. Mott

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Gridded on high density filters, a P1 genomic library of 17-fold coverage and a cosmid library of 8 genome equivalents, both made from S. pombe strain 972h-, were ordered by hybridizing genetic markers and individual clones from the two libraries. Yeast artificial chromosome (YAC) clones covering the entire genome were used to subdivide the libraries, and(More)
A complete set of software tools to aid the physical mapping of a genome has been developed and successfully applied to the genomic mapping of the fission yeast Schizosaccharomyces pombe. Two approaches were used for ordering single-copy hybridisation probes: one was based on the simulated annealing algorithm to order all probes, and another on inferring(More)
The recent observation that the mutation underlying a number of genetic diseases including fragile sites, FRAXA and FRAXE (associated with mental retardation), myotonic dystrophy, spinal and bulbar muscular atrophy (Kennedy's disease), Huntington's disease and spinocerebellar ataxia type 1 are caused by the expansion of a trinucleotide repeat sequence will(More)
A method is developed, based on word-searching, which provides a rapid test for the statistical significance of DNA sequence similarities for use in databank searching. The method makes allowance for the lengths and dinucleotide compositions of the sequences being compared. A way is also described to calculate the power of the test, i.e. the probability of(More)
Striped parrotfish (Scarus iserti) often form heterospecific groups with other reef fishes. In this study, we examined the species and body size composition of these groups on reefs in The Bahamas. Groups averaged approximately 4 S. iserti and 2 associated species, with surgeonfish (Acanthurus chirurgus and A. bahianus), slippery dick (Halichoeres(More)
We describe a program STATSEARCH which implements the method of Mott et al. (1989) for searching DNA and protein sequence databanks for statistically significant similarities to a given query sequence. STATSEARCH is written to run in conjunction with the GCG sequence analysis package.
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