Добірка наукової літератури з теми "Mapping human chromosomes"
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Статті в журналах з теми "Mapping human chromosomes"
Bentley, David R., and Ian Dunham. "Mapping human chromosomes." Current Opinion in Genetics & Development 5, no. 3 (June 1995): 328–34. http://dx.doi.org/10.1016/0959-437x(95)80047-6.
Повний текст джерелаHaig, David. "A brief history of human autosomes." Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 354, no. 1388 (August 29, 1999): 1447–70. http://dx.doi.org/10.1098/rstb.1999.0490.
Повний текст джерелаWatkins, PC, R. Eddy, Y. Fukushima, MG Byers, EH Cohen, WR Dackowski, RM Wydro, and TB Shows. "The gene for protein S maps near the centromere of human chromosome 3." Blood 71, no. 1 (January 1, 1988): 238–41. http://dx.doi.org/10.1182/blood.v71.1.238.238.
Повний текст джерелаWatkins, PC, R. Eddy, Y. Fukushima, MG Byers, EH Cohen, WR Dackowski, RM Wydro, and TB Shows. "The gene for protein S maps near the centromere of human chromosome 3." Blood 71, no. 1 (January 1, 1988): 238–41. http://dx.doi.org/10.1182/blood.v71.1.238.bloodjournal711238.
Повний текст джерелаScardino, Rita, Vanessa Milioto, Anastasia A. Proskuryakova, Natalia A. Serdyukova, Polina L. Perelman, and Francesca Dumas. "Evolution of the Human Chromosome 13 Synteny: Evolutionary Rearrangements, Plasticity, Human Disease Genes and Cancer Breakpoints." Genes 11, no. 4 (April 1, 2020): 383. http://dx.doi.org/10.3390/genes11040383.
Повний текст джерелаGoodfellow, P. N. "Mapping the Y chromosome." Development 101, Supplement (March 1, 1987): 39. http://dx.doi.org/10.1242/dev.101.supplement.39.
Повний текст джерелаMerante, Frank, Alessandra M. V. Duncan, Grant Mitchell, Catherine Duff, Joanna Rommens, and Brian H. Robinson. "Chromosomal localization of the human liver form cytochrome c oxidase subunit VIIa gene." Genome 40, no. 3 (June 1, 1997): 318–24. http://dx.doi.org/10.1139/g97-044.
Повний текст джерелаLugo, T. G., B. Handelin, A. M. Killary, D. E. Housman, and R. E. Fournier. "Isolation of microcell hybrid clones containing retroviral vector insertions into specific human chromosomes." Molecular and Cellular Biology 7, no. 8 (August 1987): 2814–20. http://dx.doi.org/10.1128/mcb.7.8.2814-2820.1987.
Повний текст джерелаLugo, T. G., B. Handelin, A. M. Killary, D. E. Housman, and R. E. Fournier. "Isolation of microcell hybrid clones containing retroviral vector insertions into specific human chromosomes." Molecular and Cellular Biology 7, no. 8 (August 1987): 2814–20. http://dx.doi.org/10.1128/mcb.7.8.2814.
Повний текст джерелаWillard, Huntington F. "The genomics of long tandem arrays of satellite DNA in the human genome." Genome 31, no. 2 (January 15, 1989): 737–44. http://dx.doi.org/10.1139/g89-132.
Повний текст джерелаДисертації з теми "Mapping human chromosomes"
Laval, S. H. "Molecular analysis of mammalian sex chromosomes." Thesis, University of Oxford, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.302954.
Повний текст джерелаKedra, Darek. "Characterization of candidate disease genes from human chromosomes 11g13 and 22q /." Stockholm, 1999. http://diss.kib.ki.se/1999/91-628-3792-3/.
Повний текст джерелаBaker, Elizabeth Gay. "The mapping of human chromosomes by fluorescence in situ hybridization /." Title page, contents and summary only, 1996. http://web4.library.adelaide.edu.au/theses/09MSM/09msmb167.pdf.
Повний текст джерелаCopies of author's previously published articles inserted. Includes bibliographical references (leaves 122-142).
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.
Знайти повний текст джерелаTypescript. Includes bibliographical references (leaves 112-128). Free to UCD Anschutz Medical Campus. Online version available via ProQuest Digital Dissertations;
Åkesson, Eva. "Genetic mapping and association analysis in multiple sclerosis /." Stockholm, 2005. http://diss.kib.ki.se/2005/91-7140-174-1/.
Повний текст джерелаWittwer, Pia Ethena. "Physical and genetical investigation of the Xp11.3 region on the short arm of the human X-chromosome." Thesis, University of the Western Cape, 2004. http://etd.uwc.ac.za/index.php?module=etd&.
Повний текст джерелаSundholm, James, and n/a. "Analysis of Specific Migraine Candidate Genes Mapping to Human Chromosome 1." Griffith University. School of Health Science, 2003. http://www4.gu.edu.au:8080/adt-root/public/adt-QGU20030829.153348.
Повний текст джерелаHolm, Sofia. "Molecular genetic studies of psoriasis susceptibility in 6p21.3 /." Stockholm, 2005. http://diss.kib.ki.se/2005/91-7140-225-X.
Повний текст джерелаLiu, Jian. "Deletion mapping of human 3P in major epithelial malignancies and fine localization of candidate tumor suppressor genes /." Stockholm, 2003. http://diss.kib.ki.se/2003/91-7349-577-8/.
Повний текст джерелаChristoffels, Alan. "Generation of a human gene index and its application to disease candidacy." Thesis, University of the Western Cape, 2001. http://etd.uwc.ac.za/index.php?module=etd&action=viewtitle&id=gen8Srv25Nme4_2413_1185436829.
Повний текст джерелаWith easy access to technology to generate expressed sequence tags (ESTs), several groups have sequenced from thousands to several thousands of ESTs. These ESTs benefit from consolidation and organization to deliver significant biological value. A number of EST projects are underway to extract maximum value from fragmented EST resources by constructing gene indices, where all transcripts are partitioned into index classes such that transcripts are put into the same index class if they represent the same gene. Therefore a gene index should ideally represent a non-redundant set of transcripts. Indeed, most gene indices aim to reconstruct the gene complement of a genome and their technological developments are directed at achieving this goal. The South African National Bioinformatics Institute (SANBI), on the other hand, embarked on the development of the sequence alignment and consensus knowledgebase (STACK) database that focused on the detection and visualisation of transcript variation in the context of developmental and pathological states, using all publicly available ESTs. Preliminary work on the STACK project employed an approach of partitioning the EST data into arbitrarily chosen tissue categories as a means of reducing the EST sequences to manageable sizes for subsequent processing. The tissue partitioning provided the template material for developing error-checking tools to analyse the information embedded in the error-laden EST sequences. However, tissue partitioning increases redundancy in the sequence data because one gene can be expressed in multiple tissues, with the result that multiple tissue partitioned transcripts will correspond to the same gene.
Therefore, the sequence data represented by each tissue category had to be merged in order to obtain a comprehensive view of expressed transcript variation across all available tissues. The need to consolidate all EST information provided the impetus for developing a STACK human gene index, also referred to as a whole-body index. In this dissertation, I report on the development of a STACK human gene index represented by consensus transcripts where all constituent ESTs sample single or multiple tissues in order to provide the correct development and pathological context for investigating sequence variation. Furthermore, the availability of a human gene index is assessed as a diseasecandidate gene discovery resource. A feasible approach to construction of a whole-body index required the ability to process error-prone EST data in excess of one million sequences (1,198,607 ESTs as of December 1998). In the absence of new clustering algorithms, at that time, we successfully ported D2_CLUSTER, an EST clustering algorithm, to the high performance shared multiprocessor machine, Origin2000. Improvements to the parallelised version of D2_CLUSTER included: (i) ability to cluster sequences on as many as 126 processors. For example, 462000 ESTs were clustered in 31 hours on 126 R10000 MHz processors, Origin2000. (ii) enhanced memory management that allowed for clustering of mRNA sequences as long as 83000 base pairs. (iii) ability to have the input sequence data accessible to all processors, allowing rapid access to the sequences. (iv) a restart module that allowed a job to be restarted if it was interrupted. The successful enhancements to the parallelised version of D2_CLUSTER, as listed above, allowed for the processing of EST datasets in excess of 1 million sequences. An hierarchical approach was adopted where 1,198,607 million ESTs from GenBank release 110 (October 1998) were partitioned into "
tissue bins"
and each tissue bin was processed through a pipeline that included masking for contaminants, clustering, assembly, assembly analysis and consensus generation. A total of 478,707 consensus transcripts were generated for all the tissue categories and these sequences served as the input data for the generation of the wholebody index sequences. The clustering of all tissue-derived consensus transcripts was followed by the collapse of each consensus sequence to its individual ESTs prior to assembly and whole-body index consensus sequence generation. The hierarchical approach demonstrated a consolidation of the input EST data from 1,198607 ESTs to 69,158 multi-sequence clusters and 162,439 singletons (or individual ESTs). Chromosomal locations were added to 25,793 whole-body index sequences through assignment of genetic markers such as radiation hybrid markers and gé
né
thon markers. The whole-body index sequences were made available to the research community through a sequence-based search engine (http://ziggy.sanbi.ac.za/~alan/researchINDEX.html).
Книги з теми "Mapping human chromosomes"
James, Louise Anne. Physical mapping on human chromosome 3 using yeast artificial chromosomes. Manchester: University of Manchester, 1994.
Знайти повний текст джерелаGindilis, V. M. Genomnai͡a︡ ėnt͡s︡iklopedii͡a︡ cheloveka: Katalog-spravochnik kartirovannykh genov. Moskva: [s.n.], 1991.
Знайти повний текст джерелаScience Writers Workshop on Biotechnology and the Human Genome (1987 Brookhaven National Laboratory). Biotechnology and the human genome: Innovations and impact. Edited by Woodhead Avril D and Barnhart Benjamin J. New York: Plenum Press, 1988.
Знайти повний текст джерелаJamie, Cuticchia A., Pearson P. L, National Center for Human Genome Research (U.S.), and International Workshop on Human Gene Mapping (11th : 1992 : Johns Hopkins Medical School), eds. Chromosome Coordinating Meeting 1992 (CCM92): Baltimore conference (1992) : update to the Eleventh International Workshop on Human Gene Mapping. Basel: Karger, 1993.
Знайти повний текст джерелаThe genome. New York, N.Y: VCH Publishers, 1990.
Знайти повний текст джерелаJean, Frézal, Klinger Harold P. 1929-, and March of Dimes Birth Defects Foundation., eds. Human gene mapping, 9: Paris Conference (1987), Ninth International Workshop on Human Gene Mapping at the University of Paris, Faculté de Médecine, France, September 6-11, 1987. Basel: Karger, 1987.
Знайти повний текст джерела1942-, Canter Charles R., ed. Biotechnology and human genetic predisposition to disease: Proceedings of a UCLA symposium held at Steamboat Springs, Colorado, March 27-April 3, 1989. New York: Wiley-Liss, 1990.
Знайти повний текст джерелаT, Strachan, and Dover G. A, eds. Human genome evolution. Oxford, England: BIOS, 1996.
Знайти повний текст джерела1939-, Read Andrew P., ed. Molecular basis of inherited disease. 2nd ed. Oxford: IRL Press at Oxford University Press, 1992.
Знайти повний текст джерелаDavies, K. E. Molecular basis of inherited disease. Oxford: IRL Press, 1988.
Знайти повний текст джерелаЧастини книг з теми "Mapping human chromosomes"
Miller, Orlando J., and Eeva Therman. "Mapping Human Chromosomes." In Human Chromosomes, 431–46. New York, NY: Springer New York, 2001. http://dx.doi.org/10.1007/978-1-4613-0139-4_29.
Повний текст джерелаTherman, Eeva. "Mapping of Human Chromosomes." In Human Chromosomes, 282–93. New York, NY: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4684-0269-8_28.
Повний текст джерелаTherman, Eeva, and Millard Susman. "Mapping of Human Chromosomes." In Human Chromosomes, 331–47. New York, NY: Springer US, 1993. http://dx.doi.org/10.1007/978-1-4684-0529-3_31.
Повний текст джерелаEvans, Glen A., and David L. McElligott. "Physical Mapping of Human Chromosomes." In Genetic Engineering, 269–78. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3424-2_15.
Повний текст джерелаFerguson-Smith, M. A. "From Chromosome Number to Chromosome Map: the contribution of human cytogenetics to genome mapping." In Chromosomes Today, 3–19. Dordrecht: Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-1510-0_1.
Повний текст джерелаHameister, H., C. Klett, G. Hartmann, and C. Ebensperger. "Comparative Gene Mapping: Human Chromosome 12 and Mouse Chromosome 15." In Chromosome 12 Aberrations in Human Solid Tumors, 73–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-662-06255-5_9.
Повний текст джерелаNance, Martha A., and Lawrence J. Schut. "Dominant Olivopontocerebellar Atrophy Mapping to Human Chromosome 6p." In Foundations of Neurology, 425–41. Boston, MA: Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3510-2_17.
Повний текст джерелаZhang, J., M. Baens, M. Chaffanet, J. Aerssens, J. J. Cassiman, and P. Marynen. "Isolation and Characterisation of NotI-end Cosmids Mapping to Human Chromosome 12p." In Chromosome 12 Aberrations in Human Solid Tumors, 173–80. Berlin, Heidelberg: Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-662-06255-5_17.
Повний текст джерелаScott, H. S., S. E. Antonarakis, L. Mittaz, M. D. Lalioti, F. Younus, A. Mohyuddin, S. Q. Mehdi, and A. Gal. "Refined Genetic Mapping of the Autosomal Recessive Non-Syndromic Deafness Locus DFNB8 on Human Chromosome 21q22.3." In Advances in Oto-Rhino-Laryngology, 158–63. Basel: KARGER, 2000. http://dx.doi.org/10.1159/000059096.
Повний текст джерелаGrigoriev, Andrei, Johan Kumlien, and Hans Lehrach. "Integrating heterogeneous datasets in genomic mapping: Radiation hybrids, YACs, genes and STS markers over the entire human chromosome X." In Bioinformatics, 106–14. Berlin, Heidelberg: Springer Berlin Heidelberg, 1996. http://dx.doi.org/10.1007/bfb0033209.
Повний текст джерелаТези доповідей конференцій з теми "Mapping human chromosomes"
Huber, P., J. Dalmon, M. Laurent, G. Courtois, D. Thevenon та G. Marguerie. "CHARACTERIZATION OFTHE 5’FLANKING REGION FOR THE HUMAN FIBRINOGEN β GENE". У XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642889.
Повний текст джерелаMills, Alea A. "Abstract IA-1: From chromosome engineering to chromatin remodeler: CHD5 is a tumor suppressor mapping to human 1p36." In Abstracts: First AACR International Conference on Frontiers in Basic Cancer Research--Oct 8–11, 2009; Boston MA. American Association for Cancer Research, 2009. http://dx.doi.org/10.1158/0008-5472.fbcr09-ia-1.
Повний текст джерелаPloos van Amstel, J. K., A. L. van der Zanden, P. H. Reitsma, and R. M. Bertina. "RESTRICTION ANALYSIS AND SOUTHERN BLOTTING OF TOTAL HUMAN DNA REVEALS THE EXISTENCE OF MORE THAN ONE GENE HOMOLOGOUS WITH PROTEIN S cDNA." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644639.
Повний текст джерелаPannekoek, H., M. Linders, J. Keijer, H. Veerman, H. Van Heerikhuizen, and D. J. Loskutoff. "THE STRUCTURE OF THE HUMAN ENDOTHELIAL PLASMINOGEN ACTIVATOR INHIBITOR (PAI-1) GENE: NON-RANDOM POSITIONING OF INTRONS." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644767.
Повний текст джерелаЗвіти організацій з теми "Mapping human chromosomes"
Antonarakis, S. E. Human Chromosome 21: Mapping of the chromosomes and cloning of cDNAs. Office of Scientific and Technical Information (OSTI), September 1991. http://dx.doi.org/10.2172/6397375.
Повний текст джерелаAntonarakis, S. E. Human chromosome 21: Linkage mapping and cloning in yeast artificial chromosomes. Office of Scientific and Technical Information (OSTI), January 1991. http://dx.doi.org/10.2172/6278130.
Повний текст джерелаYu, Bin. Statistical Problems in Remote Sensing, Image Compression, and Mapping of Human Chromosomes. Fort Belvoir, VA: Defense Technical Information Center, May 2002. http://dx.doi.org/10.21236/ada413806.
Повний текст джерелаFeldman, Moshe, Eitan Millet, Calvin O. Qualset, and Patrick E. McGuire. Mapping and Tagging by DNA Markers of Wild Emmer Alleles that Improve Quantitative Traits in Common Wheat. United States Department of Agriculture, February 2001. http://dx.doi.org/10.32747/2001.7573081.bard.
Повний текст джерелаSutherland, G. R. Physical mapping of human chromosome 16. Office of Scientific and Technical Information (OSTI), January 1992. http://dx.doi.org/10.2172/7236268.
Повний текст джерелаConnolly, Sarah. Mapping genes to human chromosome 19. Office of Scientific and Technical Information (OSTI), May 1996. http://dx.doi.org/10.2172/576741.
Повний текст джерелаCaskey, C., D. Nelson, and D. Ledbetter. Mapping and ordered cloning of the human X chromosome. Office of Scientific and Technical Information (OSTI), October 1989. http://dx.doi.org/10.2172/5518435.
Повний текст джерелаCaskey, C. T., and D. L. Nelson. Mapping and ordered cloning of the human X chromosome. Office of Scientific and Technical Information (OSTI), December 1992. http://dx.doi.org/10.2172/6387495.
Повний текст джерелаSutherland, G. R. Physical mapping of human chromosome 16. Annual progress report. Office of Scientific and Technical Information (OSTI), August 1992. http://dx.doi.org/10.2172/10167242.
Повний текст джерелаBuenaventura, J. M. The mapping of novel genes to human chromosome 19. Office of Scientific and Technical Information (OSTI), December 1994. http://dx.doi.org/10.2172/96636.
Повний текст джерела