Littérature scientifique sur le sujet « Molecular markers (SNP e SSR) »
Créez une référence correcte selon les styles APA, MLA, Chicago, Harvard et plusieurs autres
Sommaire
Consultez les listes thématiques d’articles de revues, de livres, de thèses, de rapports de conférences et d’autres sources académiques sur le sujet « Molecular markers (SNP e SSR) ».
À côté de chaque source dans la liste de références il y a un bouton « Ajouter à la bibliographie ». Cliquez sur ce bouton, et nous générerons automatiquement la référence bibliographique pour la source choisie selon votre style de citation préféré : APA, MLA, Harvard, Vancouver, Chicago, etc.
Vous pouvez aussi télécharger le texte intégral de la publication scolaire au format pdf et consulter son résumé en ligne lorsque ces informations sont inclues dans les métadonnées.
Articles de revues sur le sujet "Molecular markers (SNP e SSR)"
Khatoon, Arifa, Sumeet Verma, Gayatri Wadiye et Anuprita Zore. « Molecular markers and their potentials ». International Journal of Bioassays 5, no 01 (1 janvier 2016) : 4706. http://dx.doi.org/10.21746/ijbio.2016.01.003.
Texte intégralSa, Kyu Jin, Hyeon Park, So Jung Jang et Ju Kyong Lee. « Association Mapping of Amylose Content in Maize RIL Population Using SSR and SNP Markers ». Plants 12, no 2 (4 janvier 2023) : 239. http://dx.doi.org/10.3390/plants12020239.
Texte intégralLyu, Pin, Jianhua Hou, Haifeng Yu et Huimin Shi. « High-density Genetic Linkage Map Construction in Sunflower (Helianthus annuus L.) Using SNP and SSR Markers ». Current Bioinformatics 15, no 8 (1 janvier 2021) : 889–97. http://dx.doi.org/10.2174/1574893615666200324134725.
Texte intégralHsu, Te-Hua, Yu-Ting Chiu, Hung-Tai Lee, Hong-Yi Gong et Chang-Wen Huang. « Development of EST-Molecular Markers from RNA Sequencing for Genetic Management and Identification of Growth Traits in Potato Grouper (Epinephelus tukula) ». Biology 10, no 1 (7 janvier 2021) : 36. http://dx.doi.org/10.3390/biology10010036.
Texte intégralHsu, Te-Hua, Yu-Ting Chiu, Hung-Tai Lee, Hong-Yi Gong et Chang-Wen Huang. « Development of EST-Molecular Markers from RNA Sequencing for Genetic Management and Identification of Growth Traits in Potato Grouper (Epinephelus tukula) ». Biology 10, no 1 (7 janvier 2021) : 36. http://dx.doi.org/10.3390/biology10010036.
Texte intégralGonzaga, Zennia Jean, Kashif Aslam, Endang M. Septiningsih et Bertrand C. Y. Collard. « Evaluation of SSR and SNP Markers for Molecular Breeding in Rice ». Plant Breeding and Biotechnology 3, no 2 (30 juin 2015) : 139–52. http://dx.doi.org/10.9787/pbb.2015.3.2.139.
Texte intégralKang, Sung-Taeg, et M. A. Rouf Mian. « Genetic map of the powdery mildew resistance gene in soybean PI 243540 ». Genome 53, no 5 (mai 2010) : 400–405. http://dx.doi.org/10.1139/g10-015.
Texte intégralSusanto, Untung, Nofi Anisatun Rohmah et Made Jana Mejaya. « Distinguishing Rice Genotypes using Morphological, Agronomical »,. Jurnal Penelitian Pertanian Tanaman Pangan 34, no 2 (12 novembre 2015) : 79. http://dx.doi.org/10.21082/jpptp.v34n2.2015.p79-87.
Texte intégralFazio, Gennaro, Jack E. Staub et Sang Min Chung. « Development and Characterization of PCR Markers in Cucumber ». Journal of the American Society for Horticultural Science 127, no 4 (juillet 2002) : 545–57. http://dx.doi.org/10.21273/jashs.127.4.545.
Texte intégralWu, Jianhui, Qilin Wang, Liangsheng Xu, Xianming Chen, Bei Li, Jingmei Mu, Qingdong Zeng, Lili Huang, Dejun Han et Zhensheng Kang. « Combining Single Nucleotide Polymorphism Genotyping Array with Bulked Segregant Analysis to Map a Gene Controlling Adult Plant Resistance to Stripe Rust in Wheat Line 03031-1-5 H62 ». Phytopathology® 108, no 1 (janvier 2018) : 103–13. http://dx.doi.org/10.1094/phyto-04-17-0153-r.
Texte intégralThèses sur le sujet "Molecular markers (SNP e SSR)"
Palumbo, Fabio. « Exploiting genomics and molecular markers for plant genetics and breeding ». Doctoral thesis, Università degli studi di Padova, 2018. http://hdl.handle.net/11577/3422297.
Texte intégralI marcatori co-dominanti, tra cui i Microsatelliti (o SSR), sono strumenti molecolari ampiamente utilizzati nell’ambito della ricerca di base e applicata in specie di interesse alimentare. Tra le possibili applicazioni ricordiamo il loro impiego per studi di tracciabilità genetica di prodotti alimentari, per analisi di diversità genetica di varietà locali e identità genetica di varietà moderne e per il miglioramento genetico. Infatti gli SSR sono noti per essere altamente polimorfici e discriminanti, ben distribuiti all’interno del genoma, non influenzati da fattori ambientali, più efficienti e robusti dei marcatori fenotipici nelle analisi di diversità tra genotipi. Tuttavia, un’indagine condotta su 90 articoli scientifici basati sull’identificazione varietale delle specie economicamente più rilevanti in Italia, ha messo in luce la mancanza di un approccio comune tra gli autori in relazione alle strategie da utilizzare per questo tipo di studi. Inoltre lo studio ha evidenziato il bisogno improrogabile di stabilire procedure comuni riguardanti: i) i criteri da adottare per la scelta dei marcatori SSR ii) i parametri genetici più utili a questo scopo. Per dimostrare il potenziale di questa classe di marcatori, vengono presentati due casi studio. Il primo, che ha come oggetto Agordino, un’antica varietà locale veneta di orzo (Hordeum vulgare L.), ha permesso di enfatizzare la possibilità concreta di utilizzare i microsatelliti per la tracciabilità genetica di varietà locali ed, in particolare, di prodotti alimentari derivati. La caratterizzazione delle quattro principali varietà di mais (Zea mays L.) in Veneto -Sponcio, Marano, Biancoperla e Rosso Piave- attraverso marcatori SSR si è dimostrata invece estremamente utile per monitorare e prevenire fenomeni di erosione genetica, consentendo così di preservare la ricchezza genetica che le caratterizza, la loro identità fenotipica e i tratti qualitativi. Nonostante l’interesse economico di alcune specie, non è così raro per i ricercatori doversi interfacciare con la totale mancanza di dati SSR e, più in generale, di informazioni genomiche. Finocchio (Foeniculum vulgare Mill., 2n=2x=22), a tal proposito, rappresenta un esempio calzante. Per sopperire a questa carenza di dati, è stato condotto un sequenziamento su piattaforma Illumina Hiseq 2500, permettendo così l’assemblaggio del prima bozza del genoma di finocchio in 300408 sequenze. La successiva annotazione ha consentito quindi di individuare e caratterizzare 103306 regioni altamente ripetute. Di queste, 40 scelte in modo casuale per il disegno di primer specifici, sono state testate e 14 sono state validate su una popolazione commerciale di 118 individui potenzialmente fruibili per lo sviluppo di ibridi F1. Inoltre, il primo trascrittoma di foglia di finocchio è stato prodotto sovrapponendo due trascrittomi uno assemblato de novo e l’altro in silico, tramite allineamento sul genoma. 47775 dei 79263 trascritti totali sono stati annotati e 11853 risultano contenere una sequenza codificante completa. L’assemblaggio ha quindi consentito l’identificazione di loci coinvolti nella via biosintetica dei trans-anetolo, componente preponderante degli oli essenziali di finocchio e noto per le sue abilità nel ridurre dolori gastro-intestinali nonché per la sua attività antitrombotica e ipotensiva. Analisi dettagliate hanno infine messo in luce 1011 trascritti codificanti per fattori di trascrizione (FT), 6411 microsatelliti (EST-SSR), 3955 inserzioni/delezioni e 43237 polimorfismi a singolo nucleotide (SNP). I marcatori di tipo SNP costituiscono un’altra classe di marcatori codominanti largamente sfruttati per la caratterizzazione di geni ad eredità Mendeliana e per l’analisi di poligeni o loci codificanti tratti quantitativi (QTL). Attraverso un approccio di genotipizzazione tramite sequenziamento (GBS) è stata costruita la prima mappa genetica in radicchio (Cichorium intybus L. subsp. intybus var. foliosum, 2n=2x=18) utilizzando una popolazione BC1 (ottenuta tramite tecniche di reincrocio) segregante 1:1 per il tratto “maschio sterilità”. Questo studio ha permesso di localizzare finemente il gene nucleare della maschio sterilità Cims1 all’interno del gruppo di associazione 9 e ha consentito l’identificazione di 4 SNP co-segreganti a 0 cM con il suddetto gene. Considerato che questa forma di maschio-sterilità, controllata da un singolo allele recessivo nucleare, è uno dei metodi più efficaci per produrre ibridi F1, questi risultati saranno di estrema utilità per studi di miglioramento genetico.
Marconi, Thiago Gibbin. « Mapa funcional em cana-de-açúcar utilizando marcadores moleculares baseados em SSR e SNP ». [s.n.], 2011. http://repositorio.unicamp.br/jspui/handle/REPOSIP/316492.
Texte intégralTese (doutorado) - Universidade Estadual de Campinas, Instituto de Biologia
Made available in DSpace on 2018-08-19T06:27:16Z (GMT). No. of bitstreams: 1 Marconi_ThiagoGibbin_D.pdf: 16468359 bytes, checksum: 01e191ac164eff1d269733328f5be31e (MD5) Previous issue date: 2011
Resumo: A utilização dos marcadores moleculares em estudos de mapeamento genético e de QTLs (Quantitative Trait Loci) tem proporcionado um importante progresso no conhecimento da genética e da estrutura genômica da cana-de-açúcar. O projeto de sequenciamento de ESTs (Expressed Sequence Tags) do programa Genoma da FAPESP (SUCEST) identificou aproximadamente 43 mil clusters que representam os genes de cana-de-açúcar. Sabe-se que os ESTs apresentam grande potencial para serem utilizados no desenvolvimento de marcadores genético-moleculares. Tendo em vista os avanços possíveis no melhoramento genético da cana-de-açúcar com a construção de um mapa genético funcional a partir de ESTs de interesse, este trabalho teve como objetivos o mapeamento genético em uma população F1 de cana-de-açúcar utilizando marcadores moleculares do tipo EST-SSRs (Expressed Sequence Tags - Simple Sequence Repeats) e SNP (Single Nucleotide Polymorphism), desenvolvidos a partir de seqüências ESTs homólogas a genes de interesse. Os SNPs desenvolvidos e mapeados demonstraram novos tipos de segregações possíveis de serem incorporadas ao mapeamento genético em cana-de-açúcar, representando avanços para a análise genética de poliplóides e possibilitando a saturação do mapa genético com marcadores completamente informativos. Os marcadores moleculares EST-SSRs e SNPs desenvolvidos e integrados ao mapa genético da cana-de-açúcar aumentaram sua resolução e também as possibilidades de mapeamento dos QTLs com maior precisão
Abstract: The use of molecular markers in genetic mapping studies and QTL (Quantitative Trait Loci) has provided an important advance in knowledge of genetics and genomic structure of sugarcane. The sequencing project of ESTs (Expressed Sequence Tags) form FAPESP's Genome Program (SUCEST) identified approximately 43 000 clusters representing the sugarcane genes. It is known that the ESTs have great potential for use in the development of genetic molecular markers. Given the possible advances in genetic breeding of sugarcane with the construction of a functional genetic map from ESTs of interest, the aim of this study was the construction of a genetic map in a F1 population of sugarcane using molecular markers EST-SSR (Expressed Sequence Tags - Simple Sequence Repeats) and SNP (Single Nucleotide Polymorphism) derived from ESTs sequences homologous to genes of interest. The developed and mapped SNPs demonstrated new types of segregation ratio that could be incorporated in the genetic mapping of sugarcane, representing advances for the genetic analysis of polyploid and allowing the saturation of the genetic map with fully informative markers. The EST-SSR markers and SNPs developed and integrated into the genetic map of sugarcane increased the resolution, coverage of the genome and also the possibilities of mapping QTLs with greater precision
Doutorado
Genetica Vegetal e Melhoramento
Doutor em Genetica e Biologia Molecular
Costa, Zirlane Portugal da. « Desenvolvimento de marcadores SSR e SNP em maracujá-doce a partir de uma biblioteca enriquecida com genes de resposta à Xanthomonas axonopodis ». Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/11/11137/tde-12082014-082213/.
Texte intégralOne of the current challenges of tropical fruit research is to incorporate molecular marker-based approaches into conventional breeding programs. The sweet passion fruit (Passiflora alata) is a diploid, outcrossing and underexploited species. Recently, our group has constructed a P. alata linkage map consisted of different types of molecular markers. Moreover, we have a set of transcripts of Passiflora edulis obtained from two expression libraries: the forward and the reverse where differentially expressed transcripts were isolated from a plant inoculated with Xanthomonas axonopodis (Xap) (672), and from the control plant, uninoculated (310), respectively. Thus, in this study, this set of transcripts were exploited aiming at the development of SNP and SSR markers for future enrichment of the P. alata linkage map with putative functional markers. For the development of SSR markers, the 672 sequences from the forward library were investigated and 91 of them were found to have 115 SSRs. As expected, the trinucleotide class of repeats was the most abundant, and the (AG)n motif was the most common among the dinucleotide repeats. Primers were designed to amplify 42 of these SSRs. Transferability tests and polymorphism investigation were carried out using two accessions of P. edulis and six individuals of the mapping population of P. alata. Thirty-four primer pairs showed a good amplification pattern but only 10 loci revealed polymorphism in P. alata. For the development of SNP markers, 118 sequences selected from forward and reverse expression libraries were used for designing primers; 37 were used to assess the polymorphism in the same set of individuals of P. alata. Thirty-four biallelic SNPs were found in 16 gene fragment sequences that ranged in size from 332 to 872 bp. Considering all gene fragments, a total of 10,003 bp was obtained; the frequency of SNPs was estimated to be 1 every 294 bp. The same prevalence of SNPs (50%, 17/34) was observed within coding and non-coding regions. A putative function was assigned to all gene fragments of P. alata; 82% of them have shown homology to the original protein sequences isolated from P. edulis. Overall, the marker loci showed a low level of molecular polymorphism. This is the first report on the development of putative functional marker loci in Pasiflora using transcripts induced in response to Xap.
Pereira, Guilherme da Silva. « Desenvolvimento de marcadores SSR, M-AFLP e SNP visando à integração de mapas genético-moleculares de Passiflora alata Curtis ». Universidade de São Paulo, 2011. http://www.teses.usp.br/teses/disponiveis/11/11137/tde-17032011-105123/.
Texte intégralAlthough there is no a commercial variety of sweet passion fruit (Passiflora alata Curtis) the crop has gained importance in the Brazilian market. This justifies the use of conventional and molecular techniques for breeding the crop. In species where self-incompatibility occurs and crossing between plants is necessarily required, as in passion fruits, conventional mapping populations are not possible to be produced. Therefore, the two-way pseudo-testcross approach is used for the generation of genetic maps, employing an F1 segregating population and dominant markers, resulting in individual maps, one for each parent. The drawback of this strategy has been overcome by the use of codominant markers and more robust statistics. Markers based on SSRs (or microsatellites) and SNPs are useful for integrating the maps, because of their codominant inheritance and abundance in plant genomes. This study aimed to generate an integrated map of P. alata using new SSR, M-AFLP and SNP markers. The SSR loci were developed from an enriched genomic library previously constructed. Among the motifs, the most frequent were perfect di-nucleotides, (AC)n and (AG)n rich. In this study, 175 SSR primers were designed and evaluated along with 111 previously obtained. A polymorphism rate of 31.9% was observed between the parents. Using these primer sets, it was possible to recover single-stranded conformation polymorphisms (SSR-SSCP) at 23 loci. The genotyping of the segregating population using the 26 SSRs resulted in 40 loci; adding a SSR-SSCP, the result was six informative loci showing segregation rations of 1:1:1:1 and 1:2:1. M-AFLPs showed 34.0% of polymorphism, providing six informative loci to the map. The alignment of parental AFLP and putative gene sequences revealed one SNP per 110 bp on average. It was possible to genotype one gene-derived SNP, and primer sets for other loci are proposed. Individual maps of both parents were obtained with 175 and 229 markers segregating in 1:1 ratio, respectively, while in the integrated map were included 12, 7 and 40 markers segregating in 1:1:1:1, 1:2:1 and 3:1 rations, respectively. It was possible to establish the correspondence for most of the individual linkage groups and the integrated groups. Microsatellite-based markers showed a wide genome distribution, with eventual cluster formation. Although preliminary, this map may be useful for mapping agronomic traits and in comparison studies with the integrated map of P. edulis f. flavicarpa.
Ortega, Maria Andrea. « Identification of Molecular Markers Associated with the Rps8 locus in Soybean and Evaluation of Microsporogenesis in Rps8/rps8 Heterozygous Lines ». The Ohio State University, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=osu1259772038.
Texte intégralGettings, Katherine Butler. « Forensic Ancestry and Phenotype SNP Analysis and Integration with Established Forensic Markers ». Thesis, The George Washington University, 2013. http://pqdtopen.proquest.com/#viewpdf?dispub=3590467.
Texte intégralWhen an evidential DNA profile does not match identified suspects or profiles from available databases, further DNA analyses targeted at inferring the possible ancestral origin and phenotypic characteristics of the perpetrator could yield valuable information. Single Nucleotide Polymorphisms (SNPs), the most common form of genetic polymorphisms, have alleles associated with specific populations and/or correlated to physical characteristics. With this research, single base primer extension (SBE) technology was used to develop a 50 SNP assay designed to predict ancestry among the primary U.S. populations (African American, East Asian, European, and Hispanic/Native American), as well as pigmentation phenotype. The assay has been optimized to a sensitivity level comparable to current forensic DNA analyses, and has shown robust performance on forensic-type samples. In addition, three prediction models were developed and evaluated for ancestry in the U.S. population, and two models were compared for eye color prediction, with the best models and interpretation guidelines yielding correct information for 98% and 100% of samples, respectively. Also, because data from additional DNA markers (STR, mitochondrial and/or Y chromosome DNA) may be available for a forensic evidence sample, the possibility of including this data in the ancestry prediction was evaluated, resulting in an improved prediction with the inclusion of STR data and decreased performance when including mitochondrial or Y chromosome data. Lastly, the possibility of using next-generation sequencing (NGS) to genotype forensic STRs (and thus, the possibility of a multimarker multiplex incorporating all forensic markers) was evaluated on a new platform, with results showing the technology incapable of meeting the needs of the forensic community at this time.
Nsabiyera, Vallence. « Genetic analysis and development of molecular markers linked with rust resistance in wheat ». Thesis, The University of Sydney, 2017. http://hdl.handle.net/2123/17847.
Texte intégralMoreira, Ricardo Franco Cunha. « Estrutura genética de populações de Crinipellis perniciosa e Moniliophthora roreri utilizando marcadores RAPD e SSR / ». Jaboticabal : [s.n.], 2006. http://hdl.handle.net/11449/102837.
Texte intégralAbstract: Witches' broom and fresty pod hot, caused by Crinipellis perniciosa and Moniliophthora roreri, are the most important disease of cacao in the American Continent. Biological and molecular data have shown that these pathogen are closely related. Resistance is the most efficient method to control these diseases. Therefore, information about the population structure of these cacao pathogen are important to support the breeding programo Molecular markers such as RAPD and SSR were used to analyzed the genetic structure of C. perniciosa and M. roreri frem the American Continent. Populations of C. perniciosa clustered according to their country of origin, with more variability within than between countries, revealing the presence of subpopulations. C. perniciosa Brazilian populations presented higher genotypic diversity than C. perniciosa from other countries. The transferability of C. perniciosa-SSR to M. roreri was positive. On the contrary, high interpopulation variability was observed between Ecuador and Peru, being M. roreri from Peru much more diverse than Ecuador.
Orientador: Carlos Ruggiero
Coorientador: Karina Peres Gramacho
Banca: João Carlos de Oliveira
Banca: Antonio de Goes
Banca: Maria Lúcia Carneiro Vieira
Banca: João Alexio Scarpare Filho
Doutor
Soattin, Marica. « The use of molecular markers for analyzing genes and genomes of livestock ». Doctoral thesis, Università degli studi di Padova, 2008. http://hdl.handle.net/11577/3425494.
Texte intégralFazenda, Pedro Miguel Jesus. « Identificação de marcadores SSR e de SNPs em medronheiro (Arbutus unedo L.) por sequenciação massiva paralela ». Master's thesis, ISA, 2013. http://hdl.handle.net/10400.5/6487.
Texte intégralThe strawberry tree (Arbutus unedo L.) is native to the Mediterranean region. The use of molecular markers in this species has been limited to the use of RAPDs, ISSRs as well to the cross-amplification of SSRs from other Ericaceae. In this work, we developed a protocol for extracting nuclear DNA from the strawberry tree and performed partial next-generation sequencing of the Arbutus unedo L. genome using the "Ion Torrent" (Life Technologies) platform. The next-generation sequencing resulted in 198,856 sequences ("raw data") with an average size of 123 bp, which were uploaded to the NCBI database "Sequence Read Archive" (SRA) with the accession number: SRX341237. Data analysis led to the identification of 1085 microsatellite-containing sequences, which were also uploaded with accession numbers: from KF023636 to KF024720 to the NCBI databases. Primers were designed for 18 microsatellite loci of which only three have proved to be polymorphic in a panel of 16 samples. Based on identified 25 SNPs one CAPS marker was developed, which despite being heterozygous revealed to be monomorphic among the 16 analyzed samples.
Livres sur le sujet "Molecular markers (SNP e SSR)"
Klimenko, Irina, Nikolay Kozlov, Sergey Kostenko, Anastasia Shamustakimova et Yulian Mavlyutov. Identification and certification of forage grasses (meadow clover, alfalfa, sowing and hop) based on DNA markers. ru : Federal Williams Research Center of Forage Production and Agroecology, 2020. http://dx.doi.org/10.33814/978-5-6043194-9-9.
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 "Molecular markers (SNP e SSR)"
Ruff, Travis M., Karol Marlowe, Marcus A. Hooker, Yan Liu et Deven R. See. « Genotyping by Multiplexed Sequencing (GMS) Using SNP Markers ». Dans Methods in Molecular Biology, 9–21. New York, NY : Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3024-2_2.
Texte intégralTandon, Gitanjali, Sarika Jaiswal, Mir Asif Iquebal, Anil Rai et Dinesh Kumar. « Whole Genome Wide SSR Markers Identification Based on ddRADseq Data ». Dans Methods in Molecular Biology, 59–66. New York, NY : Springer US, 2023. http://dx.doi.org/10.1007/978-1-0716-3024-2_5.
Texte intégralHerrera, Maria del Rosario, et Marc Ghislain. « Robust and Inexpensive SSR Markers Analyses Using LI-COR DNA Analyzer ». Dans Methods in Molecular Biology, 197–205. Totowa, NJ : Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-389-3_14.
Texte intégralZhao, Yongli, Manjunath Keremane, Channapatna S. Prakash et Guohao He. « Characterization and Amplification of Gene-Based Simple Sequence Repeat (SSR) Markers in Date Palm ». Dans Methods in Molecular Biology, 259–71. New York, NY : Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7159-6_21.
Texte intégralBennetzen, Jeffrey L., Vaidyanathan Subramanian, Jichen Xu, Shanmukhaswami S. Salimath, Sujatha Subramanian, Dinakar Bhattramakki et Gary E. Hart. « A framework genetic map of sorghum containing RFLP, SSR and morphological markers ». Dans Advances in Cellular and Molecular Biology of Plants, 347–55. Dordrecht : Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-015-9815-6_20.
Texte intégralTanaka, Tsuneki, Hiroyuki Tamaki, Kazunori Ashikaga, Hiroki Fujii, Ken-ichi Tamura et Toshihiko Yamada. « Use of SSR Markers to Increase Forage Yield in Timoty (Phleum pratense L.) ». Dans Molecular Breeding of Forage and Turf, 131–42. Cham : Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-08714-6_12.
Texte intégralSretenovic Rajicic, Tatjana, Thomas Lübberstedt, Louise Bach Jensen, Uwe Scholz, W. Eberhard Weber, Andreas Graner et Klaus J. Dehmer. « Single Nucleotide Polymorphism (SNP) Markers for Allele Quantification in Lolium (Poaceae) : Development and First Applications ». Dans Molecular Breeding of Forage and Turf, 143–63. Cham : Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-08714-6_13.
Texte intégralMnasri Rahmani, Sameh, Olfa Saddoud Debbabi et Ali Ferchichi. « Efficiency of SSR Markers to Analyze the Molecular Fingerprinting of Some Tunisian Olive Cultivars ». Dans Recent Advances in Environmental Science from the Euro-Mediterranean and Surrounding Regions, 1307–9. Cham : Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-70548-4_384.
Texte intégralPratsinakis, Emmanouil D., Lefkothea Karapetsi, Symela Ntoanidou, Angelos Markos, Panagiotis Madesis, Ilias Eleftherohorinos et George Menexes. « Comparison of Hierarchical Clustering Methods for Binary Data From SSR and ISSR Molecular Markers ». Dans Data Analysis and Rationality in a Complex World, 233–41. Cham : Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-60104-1_26.
Texte intégralOnyśk, Agnieszka, et Maja Boczkowska. « M13-Tailed Simple Sequence Repeat (SSR) Markers in Studies of Genetic Diversity and Population Structure of Common Oat Germplasm ». Dans Methods in Molecular Biology, 159–68. New York, NY : Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6682-0_12.
Texte intégralActes de conférences sur le sujet "Molecular markers (SNP e SSR)"
Supari, Nurhaziqah, Yilmaz Kaya, Maral Biroudian et Muhammad Arshad Javed. « Molecular characterization of Malaysian rice cultivars using SSR markers ». Dans PROCEEDINGS OF THE 2ND INTERNATIONAL CONFERENCE ON BIOSCIENCES AND MEDICAL ENGINEERING (ICBME2019) : Towards innovative research and cross-disciplinary collaborations. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5125520.
Texte intégral« Application of SSR molecular markers in breeding and crop genetics ». Dans 2020 Conference on Social Science and Modern Science. Scholar Publishing Group, 2020. http://dx.doi.org/10.38007/proceedings.0000799.
Texte intégral« Molecular analysis of BC1F1 and BC2F1 cotton hybrids using SSR markers ». Dans Plant Genetics, Genomics, Bioinformatics, and Biotechnology. Novosibirsk ICG SB RAS 2021, 2021. http://dx.doi.org/10.18699/plantgen2021-022.
Texte intégralKARA, Karima. « MOLECULAR CHARACTERIZATION OF BREAD WHEAT GENOTYPES TRITICUM AESTIVUM L. THROUGH MICROSATELLITES SSR MARKERS ». Dans 18th International Multidisciplinary Scientific GeoConference SGEM2018. Stef92 Technology, 2018. http://dx.doi.org/10.5593/sgem2018/6.2/s25.050.
Texte intégralDuca, Maria, Ana Mutu, Ina Bivol et Steliana Clapco. « Eficiența unor marcheri moleculari în discriminarea populațiilor de lupoaie originare din China ». Dans VIIth International Scientific Conference “Genetics, Physiology and Plant Breeding”. Institute of Genetics, Physiology and Plant Protection, Republic of Moldova, 2021. http://dx.doi.org/10.53040/gppb7.2021.35.
Texte intégralBadyanov, E. V., et S. A. Ramazanova. « THE TESTING OF SSR MARKERS OF GENES CONTROLLING RESISTANCE TO P. HALSTEDII AND THE SELECTION OF OPTIMAL CONDITIONS FOR PCR ». Dans 11-я Всероссийская конференция молодых учёных и специалистов «Актуальные вопросы биологии, селекции, технологии возделывания и переработки сельскохозяйственных культур». V.S. Pustovoit All-Russian Research Institute of Oil Crops, 2021. http://dx.doi.org/10.25230/conf11-2021-19-24.
Texte intégralRapports d'organisations sur le sujet "Molecular markers (SNP e SSR)"
Zhang, Hongbin, Shahal Abbo, Weidong Chen, Amir Sherman, Dani Shtienberg et Frederick Muehlbauer. Integrative Physical and Genetic Mapping of the Chickpea Genome for Fine Mapping and Analysis of Agronomic Traits. United States Department of Agriculture, mars 2010. http://dx.doi.org/10.32747/2010.7592122.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 intégralParan, Ilan, et Molly Jahn. Analysis of Quantitative Traits in Pepper Using Molecular Markers. United States Department of Agriculture, janvier 2000. http://dx.doi.org/10.32747/2000.7570562.bard.
Texte intégralOzrenk, Koray, Gursel Ozkan, Meleksen Akin, Emine Orhan, Sadiye Peral Eyduran et Sezai Ercisli. Molecular Characterization and Genetic Relationships of Wild Apricots (Prunus Armeniaca L.) from Turkey Using SSR Markers. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, mai 2020. http://dx.doi.org/10.7546/crabs.2020.05.06.
Texte intégralVeilleux, Richard E., Jossi Hillel, A. Raymond Miller et David Levy. Molecular Analysis by SSR of Genes Associated with Alkaloid Synthesis in a Segregating Monoploid Potato Family. United States Department of Agriculture, mai 1994. http://dx.doi.org/10.32747/1994.7570550.bard.
Texte intégralRocheford, Torbert, Yaakov Tadmor, Robert Lambert et Nurit Katzir. Molecular Marker Mapping of Genes Enhancing Tocol and Carotenoid Composition of Maize Grain. United States Department of Agriculture, décembre 1995. http://dx.doi.org/10.32747/1995.7571352.bard.
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 intégralZhang, Hongbin B., David J. Bonfil et Shahal Abbo. Genomics Tools for Legume Agronomic Gene Mapping and Cloning, and Genome Analysis : Chickpea as a Model. United States Department of Agriculture, mars 2003. http://dx.doi.org/10.32747/2003.7586464.bard.
Texte intégralKatzir, Nurit, Rafael Perl-Treves et Jack E. Staub. Map Merging and Homology Studies in Cucumis Species. United States Department of Agriculture, septembre 2000. http://dx.doi.org/10.32747/2000.7575276.bard.
Texte intégralParan, Ilan, et Molly Jahn. Genetics and comparative molecular mapping of biochemical and morphological fruit characters in Capsicum. United States Department of Agriculture, mars 2005. http://dx.doi.org/10.32747/2005.7586545.bard.
Texte intégral