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Rozprawy doktorskie na temat „Genetic mapping”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 25 lipca 2025

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1

Parts, Leopold. "Genetic mapping of cellular traits." Thesis, University of Cambridge, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.609665.

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Melville, Scott Andrew Biotechnology &amp Biomolecular Sciences Faculty of Science UNSW. "Disease gene mapping in border collie dogs." Awarded by:University of New South Wales. School of Biotechnology and Biomolecular Sciences, 2006. http://handle.unsw.edu.au/1959.4/25511.

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Pedigree dog breeds are genetically isolated and inbred populations with characteristics specific to each breed. Some breeds carry genetic diseases which affect the health of the animals, but may also serve as a valuable model to identify genes involved in human disease. In the Border Collie breed in Australia, the identification of two disease genes would enable breeders to DNA test their animals and prevent future cases. Over 530 samples were collected to identify the genes responsible for these diseases through linkage mapping and candidate gene approaches. Collie Eye Anomaly (CEA) defines

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3

Einarsdottir, Elisabet. "Mapping genetic diseases in northern Sweden." Doctoral thesis, Umeå universitet, Medicinsk biovetenskap, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-499.

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The population of northern Sweden has previously been shown to be well suited for the mapping of monogenic diseases. In this thesis we have tested the hypothesis that this population could also be used for efficient identification of risk genes for common diseases. In Paper I we have hypothesised that despite the admixture of Swedish, Finnish and Sami, the northern Swedish population consists of sub-populations geographically restricted by the main river valleys running through the region. This geographic isolation, in combination with founder effects and genetic drift, could represent a uniqu

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4

Einarsdóttir, Elísabet. "Mapping genetic diseases in northern Sweden." Umeå : Department of Medical Biosciences, Umeå University, 2005. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-499.

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5

MacGregor, Stuart. "Genetic linkage mapping in complex pedigrees." Thesis, University of Edinburgh, 2003. http://hdl.handle.net/1842/12507.

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Genetic linkage analysis is the primary method for the identification of loci contributing to complex disease susceptibility. Linkage analysis techniques can be applied to both disease status (discrete traits) and to quantitative trait measures (quantitative trait loci or QTL mapping). Such techniques will be most effective if they can be applied to all of the available data; in human, ecological and livestock genetics this often means families with complex pedigree structures. The analysis of complex pedigrees is more difficult, both in terms of model formulation and computational ease, than

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6

Zenger, Kyall Richard. "Genetic linkage maps and population genetics of macropods." Phd thesis, Australia : Macquarie University, 2002. http://hdl.handle.net/1959.14/47604.

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"November 2001".<br>Thesis (PhD)--Macquarie University, Division of Environmental and Life Sciences, Department of Biological Sciences, 2002.<br>Bibliography: leaves 136-157.<br>General introduction -- Molecular markers for comparative and quantitative studies in macropods -- Genetic linkage map construction in the tammar wallaby (M. eugenii) -- Intraspecific variation, sex-biased dispersal and phylogeography of the eastern grey kangaroo (M. giganteus) -- General discussion.<br>The analysis of DNA using molecular techniques is an important tool for studies of evolutionary relationships, popula

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7

Johanneson, Bo. "Genetic Mapping of Susceptibility Genes for Systemic Lupus Erythematosus." Doctoral thesis, Uppsala University, Department of Genetics and Pathology, 2002. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-2950.

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<p>Systemic lupus erythematosus (SLE) is a complex autoimmune disease with unknown etiology. The aim of this thesis was to identify susceptibility regions through genetic mapping, using model-based linkage analysis on nuclear and extended SLE multicase families.</p><p>In the first paper we performed a genome scan on 19 genetically homogenous Icelandic and Swedish families. One region at 2q37 was identified with a significant linkage with contribution from both populations (Z=4.24). Five other regions 2q11, 4p13, 9p22, 9p13 and 9q13 showed suggestive linkage (Z>2.0).</p><p>In the second paper,

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8

Guo, Youling, and 郭友玲. "Genetic and genomic mapping of common diseases." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hub.hku.hk/bib/B50533861.

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Genome-wide mapping of susceptibility genes was conducted in two complex disorders of hypertension and epilepsy, allowing the dissection of the genetic architecture of these common diseases and related quantitative traits. The study performed comprehensive genetic analyses in a genome-wide scale, using different structure of data – sib-pairs and case-control samples. To identify genes influencing hypertension and blood pressure, a combined linkage and association study was conducted using over half a million SNPs genotyped in 328 siblings. Regions of significant linkage were identified fo

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9

Moody, Adrian John. "Mapping genetic resistance to infectious bursal disease." Thesis, University of Reading, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.326754.

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10

Duran, Alonso Maria Beatriz. "Genetic mapping of the rat agu gene." Thesis, University of Glasgow, 1997. http://theses.gla.ac.uk/39021/.

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In 1993, a mutant strain, AS/AGU arose spontaneously in an enclosed colony of the Albino Swiss (AS) strain of rat. AS/AGU animals exhibit a set of locomotor abnormalities. They display a general instability and whole body tremor, are slow at initiating movement, show reductions in purposeful action, and perform poorly at locomotor tests such as mid-air righting. L-dopa administration or fetal midbrain transplants reverse the majority of the symptoms, resembling the observations made on Parkinson's disease patients. These features make the AS/AGU strain a useful model for movement disorders due

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11

Bradley, Maria. "Genetic studies of atopic dermatitis /." Stockholm : [Karolinska institutets bibl.], 2001. http://diss.kib.ki.se/2001/91-7349-085-7/.

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12

Badenhorst, Daleen. "Development of AFLP markers for Haliotis midae for linkage mapping." Thesis, Stellenbosch : Stellenbosch University, 2008. http://hdl.handle.net/10019.1/21525.

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Thesis (MSc)--Stellenbosch University, 2008.<br>ENGLISH ABSTRACT: Haliotis midae, is the only commercially important species of the six abalone species found in South African coastal waters and has become a lucrative commercial commodity. Wild stocks of H. midae are, however, no longer commercially sustainable due to a combination of environmental factors and poaching. The solution to the crisis is artificial production systems in the form of abalone farms. An abalone enhancement programme was initiated in South Africa in 2006, funded by industry and government. This programme focuses on

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13

Köhn, Linda. "Genetic mapping of retinal degenerations in Northern Sweden." Doctoral thesis, Umeå universitet, Medicinsk och klinisk genetik, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-27004.

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Inherited retinal degenerations are a group of disorders characterised by great genetic heterogeneity. Clinically, they can be divided into two large groups of diseases, those associated with night blindness, e.g. retinitis pigmentosa (RP), and those with macular malfunction, e.g. cone/cone-rod dystrophy (COD/CORD). This thesis is focused on finding the genetic basis of disease in families with autosomal dominant COD, autosomal dominant RP, and Bothnia dystrophy (BD), a regional variant of RP. A variant of COD was previously mapped to 17p12-p13 in a family from northern Sweden. One additiona

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14

Mulley, John Charles. "Genetic marker studies in humans /." Title page, contents and summary only, 1985. http://web4.library.adelaide.edu.au/theses/09PH/09phm958.pdf.

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15

Dudley, Roy. "Genetic mapping of Armillaria ostoyae using RAPD markers." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 1998. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape10/PQDD_0004/MQ44087.pdf.

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16

Åkesson, Eva. "Genetic mapping and association analysis in multiple sclerosis /." Stockholm, 2005. http://diss.kib.ki.se/2005/91-7140-174-1/.

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17

Dudley, Roy 1972. "Genetic mapping of Armillaria ostoyae using RAPD markers." Thesis, McGill University, 1998. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=20796.

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We report here the use of RAPD-PCR (Random Amplified Polymorphic DNA - Polymerase Chain Reaction) to identify segregating loci in the haploid progeny of an Armillaria ostoyae basidiocarp and the construction of the first genetic linkage map of this fungus, one of the causal species of Armillaria Root Disease. Upon screening 75 RAPD primers, 18 were found to identify a total of 43 loci segregating with a 1 : 1 Mendelian ratio. These loci were analysed for linkage among 58 monospore progeny. The map constructed with Mapmaker (LOD = 3.0, r = 0.38) was confirmed by GMendel (LOD = 1.5, r = 0.38). T

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18

Zhuang, Nan. "Logic synthesis and technology mapping using genetic algorithms." Thesis, Imperial College London, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.286760.

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19

Stone, Caroline. "Molecular and genetic mapping of the haemochromatosis locus." Thesis, University of Oxford, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.306980.

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20

Cooper, Anneli Clare. "Linkage mapping and genetic analysis of Trypanosoma brucei." Thesis, University of Glasgow, 2010. http://theses.gla.ac.uk/1656/.

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Trypanosoma brucei is a protozoan parasite of major public health and economic importance in sub-Saharan Africa, where it is the causative agent of sleeping sickness in man and Nagana in cattle. The complete genome sequence of T.brucei is now available and the diploid genetic system has recently been demonstrated to be Mendelian. This opens up the possibility of using a classical genetic approach to identify genetic loci that determine important phenotypic traits in this parasite, such as host specificity, drug resistance, and pathogenicity. A genetic map of the non human-infective subspecies,

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21

Ahmed, Helal Uddin. "Mapping stress tolerance genetic loci in Arabidopsis thaliana." Thesis, University of Newcastle Upon Tyne, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.246628.

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22

Wang, Xiao Yu. "Genetic and physical mapping of Arabidopsis and Brassica." Thesis, University of Birmingham, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.433979.

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23

Baird, Nathan Alder. "Hypoxic gene regulation and high-throughput genetic mapping. /." Connect to title online (ProQuest), 2008. http://proquest.umi.com/pqdweb?did=1525703731&sid=1&Fmt=2&clientId=11238&RQT=309&VName=PQD.

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Thesis (Ph. D.)--University of Oregon, 2008.<br>Typescript. Includes vita and abstract. Includes bibliographical references (leaves 45-52). Also available online in ProQuest, free to University of Oregon users.

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24

Köhn, Linda. "Genetic mapping of retinal degenerations in Northern Sweden." Umeå : Umeå university, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-27004.

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25

Baird, Nathan Alder 1979. "Hypoxic gene regulation and high-throughput genetic mapping." Thesis, University of Oregon, 2008. http://hdl.handle.net/1794/7505.

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xi, 52 p. ; ill. (some col.) A print copy of this title is available through the UO Libraries under the call number: SCIENCE QH445.2 .B35 2008<br>Activation of Heat shock proteins (Hsps) is critical to adaptation to low oxygen levels (hypoxia) and enduring the oxidative stress of reoxygenation. Hsps are known to be regulated by Heat shock factor (Hsf), but my results demonstrate an unexpected regulatory link between the oxygen sensing and heat shock pathways. Hsf transcription is upregulated during hypoxia due to direct binding by Hypoxia-inducible Factor-1 (HIF-1) to HIF-1 response elem

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26

Tang, Ling-fung Paul, and 鄧凌鋒. "Dissecting the genetics of complex trait in mouse: an attempt using public resources and in-houseknockout." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2010. http://hub.hku.hk/bib/B43572170.

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27

Lambert, Carol-Ann. "A novel marker technique : using miniature inverted-repeat transposable elements (MITEs) in combination with resistant gene analogues (RGAs)." Thesis, Stellenbosch : Stellenbosch University, 2001. http://hdl.handle.net/10019.1/52117.

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Thesis (PhD)--Stellenbosch University, 2001.<br>ENGLISH ABSTRACT: Given the organisation of the maize genome as well as demands placed on the saturation of molecular linkage maps it would be desirable to identify informative molecular markers that is located or linked to genic rich areas. Sequences of gene products from different gene classes were investigated. Proteins containing a nucleotide binding site (NBS) and leucine-rich repeat (LRR) region comprise the largest class of disease resistance proteins. Resistant gene analogue (RGA) primers belonging to this specific class were derive

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28

Lehmensiek, Anke. "Genetic mapping of gray leaf spot resistance genes in maize." Thesis, Stellenbosch : Stellenbosch University, 2000. http://hdl.handle.net/10019.1/51776.

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Thesis (PhD)--Stellenbosch University, 2000.<br>ENGLISH ABSTRACT: Gray leaf spot (GLS) of maize, caused by the fungus Cercospora zeae-maydis, can reduce grain yields by up to 60% and it is now recognized as one of the most significant yield-limiting diseases of maize in many parts of the world. The most sustainable and long-term management strategy for GLS will rely heavily on the development of high-yielding, locally adapted GLS resistant hybrids. Molecular markers could be useful to plant breeders to indirectly select for genes affecting GLS resistance and to identify resistance genes

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29

Romano, Eduardo O. "Selection indices for combining marker genetic data and animal model information /." This resource online, 1993. http://scholar.lib.vt.edu/theses/available/etd-09192009-040546/.

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30

Ramburan, Viresh Premraj. "Genetic mapping of adult plant stripe rust resistance in the wheat cultivar Kariega." Thesis, Stellenbosch : Stellenbosch University, 2003. http://hdl.handle.net/10019.1/53438.

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Thesis (PhD (Agric)) -- Stellenbosch University, 2003.<br>ENGLISH ABSTRACT: Stripe (yellow) rust of wheat, caused by Puccinia striiformis f.sp. tritici, was first detected as a single introduction into South Africa in 1996. Two additional pathotypes have since been identified. Control of the disease may be achieved by use of genetic adult plant resistance (APR) as is present in the local cultivar 'Kariega'. The aim of this project was to understand the genetic basis of the APR in 'Kariega' to facilitate breeding of new varieties with genetic resistance to stripe rust. A partial linkage

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31

Magnusson, Veronica. "Genetic studies on Systemic Lupus Erythematosus : A fine mapping and candidate gene approach." Doctoral thesis, Uppsala University, Department of Genetics and Pathology, 2002. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-2869.

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<p>Linkage in the 2q37 region was evaluated using microsatellite markers in multi-case families from Sweden, Iceland and Norway. Both the two-point and the multipoint linkage analysis show highly significant LOD scores (Z=4.51 and 6.03, respectively). Linkage disequilibrium mapping indicates that some association exists in this region. The <i>PDCD1</i> gene was suggested as a candidate gene within the 2q37 locus due to its importance in immune regulation. Indeed, one haplotype, described by the presence of allele A of the PD1.3 SNP located within intron 4 of this gene, shows linkage to SLE in

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32

Dutton, Elizabeth R. "Mapping studies on mouse distal Chromosome 2." Thesis, University of Oxford, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299401.

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33

Stephens, Sarah H. "Fine mapping of the chromosome 15q13-14 schizophrenia linkage region /." Connect to full text via ProQuest. Limited to UCD Anschutz Medical Campus, 2008.

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Thesis (Ph.D. in Human Medical Genetics) -- University of Colorado Denver, 2008.<br>Typescript. Includes bibliographical references (leaves 112-128). Free to UCD Anschutz Medical Campus. Online version available via ProQuest Digital Dissertations;

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34

Thompson, Eoin. "Exclusion mapping of polycystic kidney disease: A third locus." Thesis, Edith Cowan University, Research Online, Perth, Western Australia, 1998. https://ro.ecu.edu.au/theses/1436.

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The aim of this research was to perform exclusion on a rare form of hereditary autosomal dominant polycystic kidney disease (ADPKD). To-date, two genes for ADPKD have been identified: PKDI which has been localized to the short arm of chromosome 16 and PKD2 which has been localized to the long arm of chromosome 4. However, a small number of families have been reported that have not shown linkage to either of these two loci, thus suggesting the existence of at least one additional locus (PKD3). Two families that are affected with ADPKD and do not show linkage to PKDI or PKD2 have participated in

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35

Liu, Zhiyong Michael. "Mapping physical topology with logical topology using genetic algorithm." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ62245.pdf.

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36

Craig, Nicola Jane. "Genetic and physical mapping of the rat agu locus." Thesis, University of Glasgow, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.341722.

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37

Malas, Stavros. "Genetic and physical mapping studies on mouse chromosome 2." Thesis, University College London (University of London), 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.283659.

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38

Derry, Jonathan Michael James. "Genetic and physical mapping of the mouse X chromosome." Thesis, University of Cambridge, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.239109.

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39

Fytrou, Anastasia. "Drosophila immunity : QTL mapping, genetic variation and molecular evolution." Thesis, University of Edinburgh, 2010. http://hdl.handle.net/1842/4742.

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Drosophila is involved in a wide range of interactions with parasites and pathogens (parasitoid wasps, bacteria, fungi, viruses). Drosophila hosts vary greatly at the species, population and individual level, in their response against such organisms, and much of this variation has a genetic basis. In this thesis I explored three aspects of this variation. First, using recombination mapping based on SNPs and a variation of bulk segregant analysis, I identified a QTL region on the right arm of the third chromosome of D. melanogaster associated with resistance to at least some of the parasitoid s

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40

Hanley, Steven J. "Genetic mapping of important agronomic traits in biomass willow." Thesis, University of Bristol, 2003. http://hdl.handle.net/1983/ed4da27e-641a-4d0e-bbbf-8d21493a6a29.

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41

Wu, Song. "A robust approach for genetic mapping of complex traits." [Gainesville, Fla.] : University of Florida, 2008. http://purl.fcla.edu/fcla/etd/UFE0022399.

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42

Su, Dongzhe. "Application mapping on multiprocessor hardware platforms using genetic algorithms /." View abstract or full-text, 2009. http://library.ust.hk/cgi/db/thesis.pl?CSED%202009%20SU.

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43

Saffdar, Huma. "Rust resistance in wheat: genetic analysis and molecular mapping." Thesis, The University of Sydney, 2019. https://hdl.handle.net/2123/21377.

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Breeding for rust resistance in wheat relies on detailed understanding and availability of existing genetic diversity for rust resistance among global germplasm and knowledge of pathotypic variation among rust pathogens. This study involved assessment of genetic diversity for stem rust resistance in an international wheat nursery ZWB14, inheritance of stripe rust resistance in a common wheat landrace Aus27881 and molecular mapping of stripe rust resistance in genotype ZIZ13:69 imported from International Centre for Agricultural Research in the Dry Areas (ICARDA). All stage resistance (ASR) gen

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44

Skipper, Lisa Marie. "Parkinson's disease susceptibility : genetic mapping in an isolated population." Thesis, University College London (University of London), 2005. http://discovery.ucl.ac.uk/1446678/.

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Parkinson's disease (PD) is an aetiologically complex, progressive and debilitating neurodegenerative disorder that primarily affects the elderly population. It is characterised clinically by the presence of motor symptoms including resting tremor, bradykinesia and rigidity; pathologically by neuronal loss within mid brain regions and intraneuronal inclusions comprising numerous protein aggregates. Disease risk factors are both environmental and genetic. To date, at least 10 genetic loci are implicated and specific mutations have been identified in SNCA, PRKN, UCH-Ll, DJ-1 and PINKL Variabilit

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45

Laimer, Christina. "Genetic Mapping of Increased Glutamic Acid in NOD Mice." Thesis, Umeå universitet, Biomedicinsk laboratorievetenskap, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-85070.

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46

Hsu, Ssucheng Jeff 1964. "Physical and genetic mapping on mouse proximal chromosome 18." Diss., The University of Arizona, 1998. http://hdl.handle.net/10150/282617.

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An 8-Mb yeast artificial chromosome (YAC) contig has been constructed spanning 9 cM on mouse proximal chromosome 18. The contig consists of 49 YAC clones that cover roughly 15% of the chromosome. The map was assembled based on the presence or absence of 38 DNA microsatellites, from proximal DI8Mit109 through distal D18Mit68. The physical order of those microsatellite STSs have been assigned. The locations of 21 known genes including markers near twirler (Tw) and the recently isolated Niemann-Pick type C1 (Npc1), formerly designated as spm (sphingomyelinosis), are delimited on this physical map

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47

Lorenzini, Eugenia <1993&gt. "Mapping new non-genetic dependencies in malignant pleural mesothelioma." Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2022. http://amsdottorato.unibo.it/10287/1/PhD%20Thesis%20Eugenia%20Lorenzini.pdf.

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Malignant Pleural Mesothelioma (MPM) is a very aggressive cancer whose incidence is growing worldwide. MPM escapes the classical models of carcinogenesis and lacks a distinctive genetic fingerprint, keeping obscure the molecular events that lead to tumorigenesis. This severely impacts on the limited therapeutic options and on the lack of specific biomarkers, concurring to make MPM one of the deadliest cancers. Here we combined a functional genome-wide loss of function CRISPR/Cas9 screening with patients’ transcriptomic and clinical data, to identify genes essential for MPM progression. Besid

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48

Banerjee, Samprit. "Bayesian genome-wide QTL mapping for multiple traits." Thesis, Birmingham, Ala. : University of Alabama at Birmingham, 2008. https://www.mhsl.uab.edu/dt/2009r/banerjee.pdf.

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49

Boersma, Jeffrey George. "Contributions to the molecular genetics of the Narrow-leaf Lupin (Lupinus augustifolius L.) : mapping, marker development and QTL analysis." University of Western Australia. School of Earth and Geographical Sciences, 2007. http://theses.library.uwa.edu.au/adt-WU2008.0001.

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[Truncated abstract] Narrow-leaf lupin (Lupinus angustifolius L.) was first recorded as having been introduced into Germany during the mid-19th century for use as green manuring and as fodder crops. However, it was not until post World-War I that there was any serious attempt to domesticate the species. Since that time several key domestication genes have been incorporated to enable the species to be grown as a crop over a range of climates, harvested as a bulk commodity and, the seed used for both animal and human consumption. However, the recent domestication of this species has seen a rathe

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50

Du, Plessis Jana. "Medium-throughput SNP genotyping and linkage mapping in Haliotis midae." Thesis, Stellenbosch : Stellenbosch University, 2012. http://hdl.handle.net/10019.1/71701.

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Thesis (MSc)--Stellenbosch University, 2012.<br>ENGLISH ABSTRACT: Haliotis midae (locally also known as perlemoen) is the largest of five endemic species found along the coast of South Africa. It is the only species with commercial value contributing to the exploitation of these animals. Due to declines of natural stocks, farming practices were established during the early 1990s in order to supply the international demand. To facilitate efficient breeding methods and ensure the sustainability of these commercial populations, genetic management, which can be accomplished with the use of molecul

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