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Some topics of statistical methods in gene mappingGuo, Wei, January 2006 (has links)
Thesis (Ph. D.)--University of Hong Kong, 2006. / Title proper from title frame. Also available in printed format.
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Joint relationship inference from three or more individuals in the presence of genotyping error /Sieberts, Solveig K. January 2003 (has links)
Thesis (Ph. D.)--University of Washington, 2003. / Vita. Includes bibliographical references (p. 107-111).
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Some computational problems from genomic mapping /Mumey, Brendan Marshall, January 1997 (has links)
Thesis (Ph. D.)--University of Washington, 1997. / Vita. Includes bibliographical references (p. [51]-54).
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Algorithms for DNA restriction mapping /Fasulo, Daniel. January 2000 (has links)
Thesis (Ph. D.)--University of Washington, 2000. / Vita. Includes bibliographical references (leaves 81-84).
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Molecular analysis of mammalian sex chromosomesLaval, S. H. January 1991 (has links)
No description available.
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Genome analysis in three dimensions : functional analysis of Hi-C derived datasetsSugar, Robert January 2015 (has links)
No description available.
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Molecular characterisation of translocations involving chromosome band 1p36 in acute myeloid leukaemiaSlape, Christopher Ian. January 2002 (has links) (PDF)
"October 2002" Bibliography: leaves 159-198. This thesis describes the mapping of the breakpoints of three different chromosome rearrangements, all involving 1p36, in acute myeloid leukaemia (AML) patients, and an investigation into the molecular outcomes of these rearrangements.
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Molecular characterisation of translocations involving chromosome band 1p36 in acute myeloid leukaemia / Christopher Slape.Slape, Christopher Ian January 2002 (has links)
"October 2002" / Bibliography: leaves 159-198. / xiv, 198 leaves : ill. (some col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / This thesis describes the mapping of the breakpoints of three different chromosome rearrangements, all involving 1p36, in acute myeloid leukaemia (AML) patients, and an investigation into the molecular outcomes of these rearrangements. / Thesis (Ph.D.)--University of Adelaide, Dept. of Medicine, 2003
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Use of an ovine bacterial artificial chromosome library for the study of Bovidae genomes / by Clare Alexandra Gill.Gill, Clare Alexandra January 1999 (has links)
Bibliography: leaves 206-263. / xviii, 313, [5] leaves : ill. (some col.) ; 30 cm. / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / The aim of this project was to develop tools to assist in the construction of the ovine genome map so economic trait loci in sheep can be identified. (abstract) / Thesis (Ph.D.)--University of Adelaide, Dept. of Animal Science, 2001
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Molecular characterization and genetic recombination of snakehead rhabdovirusJohnson, Marc C. 25 February 1999 (has links)
The complete genome of snakehead rhabdovirus (SHRV) was cloned and
molecularly characterized. This was initially accomplished through the sequence
determination of its glycoprotein gene and the phylogenetic analysis of this gene with
orthologous genes from other rhabdoviruses. The phylogenetic analysis revealed that
SHRV groups with viruses of the genus Novirhabdovirus. The full-length glycoprotein
was expressed in mammalian cells to investigate its potential use in the production of
pseudotyped retroviruses.
The sequence of the entire SHRV genome of 11.6 kb was determined, and all
encoded proteins, intergenic transcriptional control motifs, and the leader and trailer
regions were identified. The genome was found to encode six proteins including a
nucleoprotein, a phosphoprotein, a matrix protein, a glycoprotein, a small--presumably
non-virion--protein, and a polymerase protein. The presence of a non-virion protein,
which is the hallmark feature of all Novirhabdoviruses, supported SHRV's identity as a
member of the Novirhabdovirus genus, despite the fact that the non-virion protein
showed no homology with any known protein.
A system was developed to express a full-length, error-free positive-strand copy
of SHRV's RNA genome along with all of the SHRV proteins required for viral
replication within the cytoplasm of a virus-susceptible host cell. These factors
collectively allowed the recovery of live virus entirely from cloned cDNAs. A unique
restriction site was engineered into SHRV's cDNA genome, and the presence of this
restriction site was verified following virus recovery, proving the recovered virus was
indeed a live recombinant virus. To our knowledge this achievement marks the first time
in which reverse genetics has been performed on a nonmammalian negative-stranded
RNA virus. / Graduation date: 1999
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