Littérature scientifique sur le sujet « SNPs genotyping »
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Articles de revues sur le sujet "SNPs genotyping"
Xu, Han, Sihuan Zhang, Xiaoyan Zhang, Ruihua Dang, Chuzhao Lei, Hong Chen et Xianyong Lan. « Evaluation of novel SNPs and haplotypes within the <i>ATBF1</i> ; gene and their effects on economically important production traits in cattle ». Archives Animal Breeding 60, no 3 (29 août 2017) : 285–96. http://dx.doi.org/10.5194/aab-60-285-2017.
Texte intégralClaassen, Daniel O., Jody Corey-Bloom, E. Ray Dorsey, Mary Edmondson, Sandra K. Kostyk, Mark S. LeDoux, Ralf Reilmann et al. « Genotyping single nucleotide polymorphisms for allele-selective therapy in Huntington disease ». Neurology Genetics 6, no 3 (14 mai 2020) : e430. http://dx.doi.org/10.1212/nxg.0000000000000430.
Texte intégralMin, Josine L., Nico Lakenberg, Margreet Bakker-Verweij, Eka Suchiman, Dorret I. Boomsma, P. Eline Slagboom et Ingrid Meulenbelt. « High Microsatellite and SNP Genotyping Success Rates Established in a Large Number of Genomic DNA Samples Extracted From Mouth Swabs and Genotypes ». Twin Research and Human Genetics 9, no 4 (1 août 2006) : 501–6. http://dx.doi.org/10.1375/twin.9.4.501.
Texte intégralRustgi, S., R. Bandopadhyay, H. S. Balyan et P. K. Gupta. « EST-SNPs in bread wheat : discovery, validation, genotyping and haplotype structure ». Czech Journal of Genetics and Plant Breeding 45, No. 3 (6 octobre 2009) : 106–16. http://dx.doi.org/10.17221/16/2009-cjgpb.
Texte intégralLi, Peng-Le, Mo-Hua Yang, Xiao-Long Jiang, Huan Xiong, Hui-Liang Duan, Feng-Lan Zou, Qian-Yu Xu, Wei Wang, Yong-Hui Hong et Neng-Qing Lin. « De Novo SNP Discovery and Genotyping of Masson Pine (Pinus massoniana Lamb.) via Genotyping-by-Sequencing ». Forests 14, no 2 (14 février 2023) : 387. http://dx.doi.org/10.3390/f14020387.
Texte intégralCalvo, Jorge H., Magdalena Serrano, Flavie Tortereau, Pilar Sarto, Laura P. Iguacel, María A. Jiménez, José Folch, José L. Alabart, Stéphane Fabre et Belén Lahoz. « Development of a SNP parentage assignment panel in some North-Eastern Spanish meat sheep breeds ». Spanish Journal of Agricultural Research 18, no 4 (27 octobre 2020) : e0406. http://dx.doi.org/10.5424/sjar/2020184-16805.
Texte intégralGraham, Natalie, Emily Telfer, Tancred Frickey, Gancho Slavov, Ahmed Ismael, Jaroslav Klápště et Heidi Dungey. « Development and Validation of a 36K SNP Array for Radiata Pine (Pinus radiata D.Don) ». Forests 13, no 2 (24 janvier 2022) : 176. http://dx.doi.org/10.3390/f13020176.
Texte intégralChiapparino, E., D. Lee et P. Donini. « Genotyping single nucleotide polymorphisms in barley by tetra-primer ARMS–PCR ». Genome 47, no 2 (1 avril 2004) : 414–20. http://dx.doi.org/10.1139/g03-130.
Texte intégralGermer, Søren, et Russell Higuchi. « Single-Tube Genotyping without Oligonucleotide Probes ». Genome Research 9, no 1 (1 janvier 1999) : 72–78. http://dx.doi.org/10.1101/gr.9.1.72.
Texte intégralAhmed, Mahbubl, Chee Goh, Edward Saunders, Clara Cieza-Borrella, Zsofia Kote-Jarai, Fredrick R. Schumacher et Ros Eeles. « Germline genetic variation in prostate susceptibility does not predict outcomes in the chemoprevention trials PCPT and SELECT ». Prostate Cancer and Prostatic Diseases 23, no 2 (27 novembre 2019) : 333–42. http://dx.doi.org/10.1038/s41391-019-0181-y.
Texte intégralThèses sur le sujet "SNPs genotyping"
Simmons, Stacy. « Genotyping for Response to Physical Training ». Wright State University / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright1565880927061102.
Texte intégralHammond, Naomi Rachel. « Improved approaches to multiplexed PCR and to the genotyping of SNPs by mass spectrometry ». Thesis, University of Southampton, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.438509.
Texte intégralChacon, Cortes Diego Fernando. « Study of miRNA polymorphisms and their potential association with breast cancer risk in Australian Caucasian populations ». Thesis, Queensland University of Technology, 2015. https://eprints.qut.edu.au/89768/15/89768%28thesis%29.pdf.
Texte intégralMerchant-Patel, Shreema. « Development of rapid and highly resolving combinatorial genotyping schemes for Campylobacter jejuni and Campylobacter coli ». Thesis, Queensland University of Technology, 2009. https://eprints.qut.edu.au/33194/1/Shreema_Merchant-Patel_Thesis.pdf.
Texte intégralSöderholm, Simon. « The Complex Genetics of Multiple Sclerosis : A preliminary study of MS-associated SNPs prior to a larger genotyping project ». Thesis, Linköpings universitet, Institutionen för fysik, kemi och biologi, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-129423.
Texte intégralCarvalho, Thaysa Buss. « Avaliação de SNPs (Single Nucleotide Polymorphisms) nas diferentes formas clínicas da doença de Chagas ». Universidade Estadual Paulista (UNESP), 2018. http://hdl.handle.net/11449/152931.
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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
A doença de Chagas (DC), causada pelo protozoário Trypanosoma cruzi (T. cruzi), ainda é considerada como um problema de saúde pública em muitos países da América Latina. De acordo com a Organização Mundial da Saúde, estima-se que entre seis a sete milhões de pessoas no mundo estejam infectadas. Indivíduos na fase crônica da doença podem ser classificados como assintomáticos ou sintomáticos (estes, desenvolvendo as formas clínicas cardíaca, digestiva ou mista). Os assintomáticos correspondem a 70% dos indivíduos nessa fase e, embora apresentem sorologia positiva para anticorpos anti T-cruzi, não desenvolvem manifestações clínicas da doença. O motivo pelo qual alguns pacientes permanecem assintomáticos, e outros desenvolvem sintomas severos, ainda é desconhecido. Fatores genéticos do hospedeiro são bastante relevantes e podem explicar a heterogeneidade encontrada em pacientes que vivem com a doença em áreas endêmicas. Diante disso, o presente trabalho teve como objetivo avaliar SNPs (Single Nucleotide Polymorphisms) no gene TNF-α (rs1800629) e ACAT-1 (rs1044925) em indivíduos com DC crônica e verificar se os mesmos estão relacionados com a susceptibilidade para manifestação de formas clínicas sintomáticas com uso da técnica PCR-RFLP. Foram genotipadas 124 amostras para o gene TNF-α e 135 para o gene ACAT-1. Foi observada associação significativa da presença do alelo A do gene TNF- α em indivíduos sintomáticos em relação aos assintomáticos (p = 0,045). Também houve associação significativa entre o alelo G (p = 0,008) e o genótipo GG (p = 0,001) do gene TNF-α e os genótipos AA (p = 0,047) e AC (p = 0,016) do gene ACAT-1 nos indivíduos assintomáticos em relação aos sintomáticos. Nossos resultados sugerem que a presença do alelo A do gene TNF-α possa estar relacionada com a presença de manifestações clínicas sintomáticas na fase crônica da doença e o alelo G, bem como, genótipo GG possam estar associados com ausência de sintomas clínicos em indivíduos nessa fase. A respeito do SNP do gene ACAT-1, nossos dados sugerem efeito protetor dos genótipos AA e AC segundo apresentação de sintomas da doença na fase crônica, o que representa dado inédito em chagásicos.
Chagas disease (CD), caused by the protozoan Trypanosoma cruzi (T. cruzi), is still considered a public health problem in many Latin America countries. According to the World Health Organization, it is estimated that between six and seven million people worldwide are infected. Disease’s chronic phase individuals may be classified as asymptomatic or symptomatic (these, developing as clinical cardiac, digestive or mixed forms). Asymptomatic individuals account for 70% of the patients at this stage and, although they have positive serology for anti-T-cruzi antibodies, they do not develop it’s clinical manifestations. The reason why some patients remain asymptomatic, and others develop severe symptoms, is still unknown. Host’s genetic factors are quite relevant and may explain the heterogeneity found in patients living with the disease in endemic areas. The objective of this study was to evaluate SNPs in the TNF-α (rs1800629) and ACAT-1 (rs1044925) genes in individuals with chronic CD and to verify if the polymorphisms are related to the susceptibility to manifestation of symptomatic clinical forms using the PCR-RFLP technique. Were genotyped 124 samples for the TNF-α gene and 135 for the ACAT-1 gene. Significant association for the presence of the A allele of the TNF-α gene was observed for symptomatic individuals in relation to the asymptomatic ones (p = 0.045). There was also a significant association between the G allele (p = 0.008) and the GG genotype (p = 0.001) of the TNF-α gene and the AA (p = 0.047) and AC (p = 0.016) genotypes of the ACAT-1 gene for asymptomatic patients. Our results suggests that the presence of the TNF-α gene A allele may be related to the presence of symptomatic clinical manifestations in the chronic phase of the disease and the G allele as well as the GG genotype may be associated with absence of clinical symptoms in individuals at this stage. Regarding the ACAT-1 gene SNP, our data suggests a protective effect of AA and AC genotypes according to the to the presentation of chronic disease symptoms, which is an unprecedented finding in chagasic patients.
CAPES: 1578310
Stephens, Alex J. « The development of rapid genotyping methods for methicillin-resistant Staphylococcus aureus ». Thesis, Queensland University of Technology, 2008. https://eprints.qut.edu.au/20172/1/Alexander_Stephens_Thesis.pdf.
Texte intégralStephens, Alex J. « The development of rapid genotyping methods for methicillin-resistant Staphylococcus aureus ». Queensland University of Technology, 2008. http://eprints.qut.edu.au/20172/.
Texte intégralMontes, Vergara Donicer Eduardo [UNESP]. « Prospecção de assinaturas de seleção em regiões de QTL associadas com características reprodutivas em novilhas Nelore ». Universidade Estadual Paulista (UNESP), 2016. http://hdl.handle.net/11449/137897.
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Características reprodutivas, como a ocorrência de prenhez precoce, são mais importantes economicamente ao comparar-se com as características de crescimento. Desta forma, o aumento da taxa de fertilidade e emprego de animais geneticamente superiores é determinante no progresso da produtividade nas fazendas comerciais de produção de carne bovina. A seleção modifica as frequências alélicas de uma população ao transmitir as variantes gênicas mais interessantes. Considerando o desequilíbrio de ligação, alguns locos adjacentes às mutações favoráveis são transmitidos ao longo das gerações. Estes são conhecidos como assinaturas de seleção e podem ser identificados com o uso de “chips” de SNP e metodologias estatísticas adequadas. Com o objetivo de identificar assinaturas de seleção recentes em QTL previamente mapeados para características reprodutivas de fêmeas bovinas ligadas à precocidade sexual, foram genotipadas 2.035 fêmeas da raça Nelore (Bos taurus indicus) com o chip “Illumina BovineHD BeadChip”. Posteriormente foi inferida a fase de ligação dos SNPs e a reconstrução dos haplótipos. A detecção de assinaturas de seleção foi realizada por meio da aplicação da metodologia “Relative Extended Haplotype Homozygosity” (REHH). A identificação de genes que contribuem para a importância da característica nestas regiões foi feita com a ferramenta Map Viewer do “National Center for Biotechnology Information”- NCBI e GBrowse carregada com o genoma bovino versão UMD 3.1. Foram detectadas 2.756 regiões núcleo, com tamanho médio 27,6 ± 29,1 Kb, abrangendo 70,1 Mb dos 25 cromossomos estudados. Dos SNPs utilizados, 17.312 participaram da formação das regiões núcleo, com o mínimo de 10 no BTA27 e o máximo de 20 SNPs nos cromossomos 1, 3-7, 9-15,18-21, e 23-24. Foram identificadas 40 assinaturas de seleção recentes com diferentes níveis de significância e 56 genes A maioria dos genes localizados nas regiões de assinaturas de seleção tem relação com os processos biológicos de metabolismo mitocondrial, desenvolvimento pós-embrionário, regulação da taxa de ovulação e fertilidade, resposta imune, metabolismo de triglicerídeo, proliferação celular e neurônios receptores olfativos. A investigação de mecanismos regulatórios da expressão dos genes associados aos processos biológicos descritos pode oferecer conhecimentos sobre os mecanismos moleculares que afetam a característica ocorrências de prenhez precoce, na raça Nelore.
Some reproductive traits such as early pregnancy are more profitable than those related to growth. Increasing fertility rate and using genetically superior animals are crucial in productivity of meat commercial farms. Artificial selection modifies allele frequencies of a cattle population by transmitting the most significant gene variants. Considering linkage disequilibrium, some loci adjacent to favorable mutations are transmitted across generations. Known as signatures of selection, such locations can be identified by the SNP chips, and appropriate statistical methods. To determine recent selection signature in quantitative trait loci (QTL) previously mapped for reproductive cow features linked to sexual precocity, 2,035 Nelore (Bos taurus indicus) females were genotyped by Illumina Bovine chip. After, inferring the connection phase of SNPs allowed haplotype reconstruction. Selection signatures were detected by Relative Extended Haplotype Homozygosity (REHH) method. Genes supposedly important were recognized by Map Viewer from the National Center for Biotechnology Information (NCBI), and also through a loaded GBrowse with bovine genome UMD, version 3.1. A total of 2,756 core regions were detected, with an average size of 27.6 ± 29.1 Kb, covering 70.1 Mb of 25 chromosomes. 17,312 SNPs are involved in the formation of core regions with at least 10 on BTA27, and a maximum of 20 SNPs on 1, 3-7, 9-15, 18-21, and 23-24 chromosomes. We identify 40 possible recent selection signatures, with different levels of significance, and 56 positional candidate genes. Most of genes located in selection signature regions are related to biological processes of mitochondrial metabolism, post-embryonic development, ovulation rate regulation and fertility, immune response, triglyceride metabolism, cell proliferation, and olfactory receptor neurons. The investigation of regulatory mechanisms of gene expression associated with biological processes described can provide knowledge on the molecular mechanisms affecting characteristic of early pregnancy occurrences in Nellore.
Price, Erin Peta. « Development of novel combinatorial methods for genotyping the common foodborne pathogen Campylobacter jejuni ». Thesis, Queensland University of Technology, 2007. https://eprints.qut.edu.au/16601/1/Erin_Peta_Price_Thesis.pdf.
Texte intégralLivres sur le sujet "SNPs genotyping"
Henry, R. J., dir. Plant genotyping II : SNP technology. Wallingford : CABI, 2008. http://dx.doi.org/10.1079/9781845933821.0000.
Texte intégralJ, Henry Robert, dir. Plant genotyping II : SNP technology. Wallingford, UK : CABI, 2008.
Trouver le texte intégral1962-, Hajeer Ali, Worthington Jane 1961- et John Sally 1964-, dir. SNP and microsatellite genotyping : Markers for genetic analysis. Natick, MA : Eaton Pub., 2000.
Trouver le texte intégralLewis, Myles, et Tim Vyse. Genetics of connective tissue diseases. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0042.
Texte intégralEyre, Steve, et Jane Worthington. Genetics of rheumatoid arthritis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0040.
Texte intégralEyre, Steve, Jane Worthington et Sebastien Viatte. Genetics of rheumatoid arthritis. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199642489.003.0040_update_003.
Texte intégralHajeer, Ali. Snp And Microsatellite Genotyping : Markers For Genetic Analysis (MOLECULAR LABORATORY METHODS (BIOTECHNIQUES BOOKS)). EATON PUBLISHING, 2000.
Trouver le texte intégralChapitres de livres sur le sujet "SNPs genotyping"
Barreiro, Luis B., Ricardo Henriques et Musa M. Mhlanga. « High-Throughput SNP Genotyping : Combining Tag SNPs and Molecular Beacons ». Dans Methods in Molecular Biology, 255–76. Totowa, NJ : Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-411-1_17.
Texte intégralBortolin, Susan. « Multiplex Genotyping for Thrombophilia-Associated SNPs by Universal Bead Arrays ». Dans DNA and RNA Profiling in Human Blood, 59–72. Totowa, NJ : Humana Press, 2008. http://dx.doi.org/10.1007/978-1-59745-553-4_6.
Texte intégralDabrowski, Piotr Wojciech, Kati Bourquain et Andreas Nitsche. « Multiplex Pyrosequencing® : Simultaneous Genotyping Based on SNPs from Distant Genomic Regions ». Dans Methods in Molecular Biology, 337–47. New York, NY : Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2715-9_23.
Texte intégralBayer, Philipp Emanuel. « Skim-Based Genotyping by Sequencing Using a Double Haploid Population to Call SNPs, Infer Gene Conversions, and Improve Genome Assemblies ». Dans Plant Bioinformatics, 285–92. New York, NY : Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3167-5_16.
Texte intégralBayer, Philipp Emanuel. « Skim-Based Genotyping by Sequencing Using a Double Haploid Population to Call SNPs, Infer Gene Conversions, and Improve Genome Assemblies ». Dans Plant Bioinformatics, 405–13. New York, NY : Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2067-0_20.
Texte intégralPeatman, Eric. « SNP Genotyping Platforms ». Dans Next Generation Sequencing and Whole Genome Selection in Aquaculture, 123–32. Oxford, UK : Wiley-Blackwell, 2010. http://dx.doi.org/10.1002/9780470958964.ch8.
Texte intégralStuder, Bruno, et Roland Kölliker. « SNP Genotyping Technologies ». Dans Diagnostics in Plant Breeding, 187–210. Dordrecht : Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-5687-8_9.
Texte intégralRoyo, Jose Luis, et Jose Jorge Galán. « Pyrosequencing for SNP Genotyping ». Dans Methods in Molecular Biology, 123–33. Totowa, NJ : Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-411-1_7.
Texte intégralSingh, B. D., et A. K. Singh. « High-Throughput SNP Genotyping ». Dans Marker-Assisted Plant Breeding : Principles and Practices, 367–400. New Delhi : Springer India, 2015. http://dx.doi.org/10.1007/978-81-322-2316-0_13.
Texte intégralMohanrao, Manmode Darpan, Senapathy Senthilvel, Yarabapani Rushwanth Reddy, Chippa Anil Kumar et Palchamy Kadirvel. « Amplifluor-Based SNP Genotyping ». Dans Methods in Molecular Biology, 191–200. New York, NY : Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3024-2_13.
Texte intégralActes de conférences sur le sujet "SNPs genotyping"
Ma, Jie, Sheng Ning et Pengfeng Xiao. « Multiple SNPs genotyping by ligation of universal probes on 3D DNA microarray ». Dans 2010 3rd International Conference on Biomedical Engineering and Informatics (BMEI). IEEE, 2010. http://dx.doi.org/10.1109/bmei.2010.5639397.
Texte intégralLee, Y. L., M. Bosse, W. Coppieters, R. F. Veerkamp, L. Karim, C. Oget-Ebrad, T. Druet et al. « 542. Rare CNVs in the bovine genome are not captured well by 50K density genotyping array SNPs ». Dans World Congress on Genetics Applied to Livestock Production. The Netherlands : Wageningen Academic Publishers, 2022. http://dx.doi.org/10.3920/978-90-8686-940-4_542.
Texte intégralSharma, Vineeta, Pallavi Singhal, Anoop Kumar, V. G. Ramachandran, Shukla Das et Mausumi Bharadwaj. « Association of TNF-α–rs 281865419 polymorphism with reproductive tract infections in Indian population ». Dans 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685357.
Texte intégralSharma, Vineeta, Pallavi Singhal, Anoop Kumar, V. G. Ramachandran, Shukla Das et Mausumi Bharadwaj. « Association of TNF-α rs-281865419 polymorphism with reproductive tract infections in Indian population ». Dans 16th Annual International Conference RGCON. Thieme Medical and Scientific Publishers Private Ltd., 2016. http://dx.doi.org/10.1055/s-0039-1685270.
Texte intégralSHARAN, R., A. BEN-DOR et Z. YAKHINI. « MULTIPLEXING SCHEMES FOR GENERIC SNP GENOTYPING ASSAYS ». Dans Proceedings of the Pacific Symposium. WORLD SCIENTIFIC, 2003. http://dx.doi.org/10.1142/9789812704856_0014.
Texte intégralMachado, Vitor Pereira, Edis Bellini Júnior, Lucas Gazarini, Clarisse Lobo et Claudia Bonini-Domingos. « Association of genetic markers with ischemic stroke in pediatric patients with sickle cell anemia ». Dans XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.293.
Texte intégralOscoz Irurozqui, Maitane, Maria Guardiola-Ripoll, Carmen Almodóvar-Payà, Salavador Sarró, Amalia Guerrero-Pedraza, Edith Pomarol-Clotet et Mar Fatjó-Vilas. « Cannabis use and genes of endocannabinoid system : their role in psychotic symptoms and cognition in first-episode psychosis. » Dans 22° Congreso de la Sociedad Española de Patología Dual (SEPD) 2020. SEPD, 2020. http://dx.doi.org/10.17579/sepd2020o031.
Texte intégral« PROPOSAL FOR A FILTERLESS FLUORESCENCE SENSOR FOR SNP GENOTYPING ». Dans International Conference on Biomedical Electronics and Devices. SciTePress - Science and and Technology Publications, 2012. http://dx.doi.org/10.5220/0003774201850189.
Texte intégral« Application of Amplifluor-like SNP markers in plant genotyping ». Dans Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Institute of Cytology and Genetics, Siberian Branch of the Russian Academy of Sciences, 2019. http://dx.doi.org/10.18699/plantgen2019-162.
Texte intégralLiu, Zheng, Bin Liu, Yan Deng et Nongyue He. « The state of field of high-throughput SNP genotyping system ». Dans 2011 International Symposium on Bioelectronics and Bioinformatics (ISBB). IEEE, 2011. http://dx.doi.org/10.1109/isbb.2011.6107674.
Texte intégralRapports d'organisations sur le sujet "SNPs genotyping"
Hultman, Keith, et Eve Mellgren. Fetching SNPs : A Dog Genotyping Laboratory for Undergraduate Biology. Genetics Society of America Peer-Reviewed Education Portal, septembre 2014. http://dx.doi.org/10.1534/gsaprep.2014.001.
Texte intégralMedrano, Juan, Adam Friedmann, Moshe (Morris) Soller, Ehud Lipkin et Abraham Korol. High resolution linkage disequilibrium mapping of QTL affecting milk production traits in Israel Holstein dairy cattle. United States Department of Agriculture, mars 2008. http://dx.doi.org/10.32747/2008.7696509.bard.
Texte intégralSela, Hanan, Eduard Akhunov et Brian J. Steffenson. Population genomics, linkage disequilibrium and association mapping of stripe rust resistance genes in wild emmer wheat, Triticum turgidum ssp. dicoccoides. United States Department of Agriculture, janvier 2014. http://dx.doi.org/10.32747/2014.7598170.bard.
Texte intégralHassen, Abebe T., Jack C. M. Dekkers, Susan J. Lamont, Rohan L. Fernando, Santiago Avendano, John Ralph, Jim McKay et William G. Hill. High-density SNP Genotyping Analysis of Broiler Breeding Lines. Ames (Iowa) : Iowa State University, janvier 2007. http://dx.doi.org/10.31274/ans_air-180814-1049.
Texte intégralBreiman, Adina, Jan Dvorak, Abraham Korol et Eduard Akhunov. Population Genomics and Association Mapping of Disease Resistance Genes in Israeli Populations of Wild Relatives of Wheat, Triticum dicoccoides and Aegilops speltoides. United States Department of Agriculture, décembre 2011. http://dx.doi.org/10.32747/2011.7697121.bard.
Texte intégralSaatchi, Mahdi, et Dorian J. Garrick. Developing a Reduced SNP Panel for Low-cost Genotyping in Beef Cattle. Ames (Iowa) : Iowa State University, janvier 2014. http://dx.doi.org/10.31274/ans_air-180814-1140.
Texte intégralGorbach, Danielle M., Bin Fan, Suneel K. Onteru, Xia Zhao, Zhi-Qiang Du, Dorian J. Garrick, Jack C. M. Dekkers et Max F. Rothschild. Genome-Wide Association Studies for Important Economic Traits in Domestic Animals Using High Density SNP Genotyping. Ames (Iowa) : Iowa State University, janvier 2010. http://dx.doi.org/10.31274/ans_air-180814-980.
Texte intégralJoel, Daniel M., Steven J. Knapp et Yaakov Tadmor. Genomic Approaches for Understanding Virulence and Resistance in the Sunflower-Orobanche Host-Parasite Interaction. United States Department of Agriculture, août 2011. http://dx.doi.org/10.32747/2011.7592655.bard.
Texte intégralHovav, Ran, Peggy Ozias-Akins et Scott A. Jackson. The genetics of pod-filling in peanut under water-limiting conditions. United States Department of Agriculture, janvier 2012. http://dx.doi.org/10.32747/2012.7597923.bard.
Texte intégralGur, Amit, Edward Buckler, Joseph Burger, Yaakov Tadmor et Iftach Klapp. Characterization of genetic variation and yield heterosis in Cucumis melo. United States Department of Agriculture, janvier 2016. http://dx.doi.org/10.32747/2016.7600047.bard.
Texte intégral