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Статті в журналах з теми "Gene overlaps"
Decrulle, Antoine L., Antoine Frénoy, Thomas A. Meiller-Legrand, Aude Bernheim, Chantal Lotton, Arnaud Gutierrez, and Ariel B. Lindner. "Engineering gene overlaps to sustain genetic constructs in vivo." PLOS Computational Biology 17, no. 10 (October 8, 2021): e1009475. http://dx.doi.org/10.1371/journal.pcbi.1009475.
Повний текст джерелаMuñoz-Baena, Laura, and Art F. Y. Poon. "Using networks to analyze and visualize the distribution of overlapping genes in virus genomes." PLOS Pathogens 18, no. 2 (February 24, 2022): e1010331. http://dx.doi.org/10.1371/journal.ppat.1010331.
Повний текст джерелаLartey, R. T., T. C. Voss, and U. Melcher. "Tobamovirus evolution: gene overlaps, recombination, and taxonomic implications." Molecular Biology and Evolution 13, no. 10 (December 1, 1996): 1327–38. http://dx.doi.org/10.1093/oxfordjournals.molbev.a025579.
Повний текст джерелаMakałowska, Izabela, Chiao-Feng Lin, and Krisitina Hernandez. "Birth and death of gene overlaps in vertebrates." BMC Evolutionary Biology 7, no. 1 (2007): 193. http://dx.doi.org/10.1186/1471-2148-7-193.
Повний текст джерелаJain, Kanika, Tyler H. Stanage, Elizabeth A. Wood, and Michael M. Cox. "The Escherichia coli serS gene promoter region overlaps with the rarA gene." PLOS ONE 17, no. 4 (April 15, 2022): e0260282. http://dx.doi.org/10.1371/journal.pone.0260282.
Повний текст джерелаPribyl, T., C. Campagnoni, S. Amur-Umarjee, K. Kampf, B. Garbay, V. Handley, and A. Campagnoni. "Identification and characterization of Golli, a gene which overlaps the MBP gene." Neurochemistry International 21 (January 1992): C1. http://dx.doi.org/10.1016/0197-0186(92)92037-5.
Повний текст джерелаBrauburger, Kristina, Yannik Boehmann, Verena Krähling, and Elke Mühlberger. "Transcriptional Regulation in Ebola Virus: Effects of Gene Border Structure and Regulatory Elements on Gene Expression and Polymerase Scanning Behavior." Journal of Virology 90, no. 4 (December 9, 2015): 1898–909. http://dx.doi.org/10.1128/jvi.02341-15.
Повний текст джерелаKepler, T. B., M. Borrero, B. Rugerio, S. K. McCray, and S. H. Clarke. "Interdependence of N nucleotide addition and recombination site choice in V(D)J rearrangement." Journal of Immunology 157, no. 10 (November 15, 1996): 4451–57. http://dx.doi.org/10.4049/jimmunol.157.10.4451.
Повний текст джерелаChen, Quan, Xianghong J. Zhou, and Fengzhu Sun. "Finding Genetic Overlaps Among Diseases Based on Ranked Gene Lists." Journal of Computational Biology 22, no. 2 (February 2015): 111–23. http://dx.doi.org/10.1089/cmb.2014.0149.
Повний текст джерелаRay, Bryan L., Charles I. White, and James E. Haber. "The TSM1 gene of Saccharomyces cerevisiae overlaps the MAT locus." Current Genetics 20, no. 1-2 (July 1991): 25–31. http://dx.doi.org/10.1007/bf00312761.
Повний текст джерелаДисертації з теми "Gene overlaps"
Reich, Jennifer G. "Functional overlap in gene duplications in the yeast Saccharomyces cerevisiae." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2001. http://www.collectionscanada.ca/obj/s4/f2/dsk3/ftp04/MQ59268.pdf.
Повний текст джерелаLi, Ai. "Generalizations of the topological overlap measure for neighborhood analysis and module detection in gene and protein networks." Diss., Restricted to subscribing institutions, 2007. http://proquest.umi.com/pqdweb?did=1481673641&sid=1&Fmt=2&clientId=1564&RQT=309&VName=PQD.
Повний текст джерелаSilva, Alex Eduardo da. "Avaliação genotípica de pacientes com polineuropatia inflamatória desmielinizante crônica: estudo da duplicação/deleção do gene PMP22." Universidade de São Paulo, 2014. http://www.teses.usp.br/teses/disponiveis/17/17140/tde-25112014-142430/.
Повний текст джерелаIntroduction: Polyneuropathies are peripheral nervous system disorders with a wide range of etiologies. Among them, inflammatory and hereditary are frequent with prevalence of 0.67-7.7/100000 and 7.9-82.3/100000, for chronic inflammatory demyelinating polyneuropathy (CIDP) and Charcot-Marie-Tooth disease (CMT), respectively. There are a few evidence of ovelapping between these two conditions and also some diagnostic difficulties in specific situations. Objectives: To study the frequency of mutations in PMP22 gene (duplications and delections) among a cohort of patients initially diagnosed as CIDP or suspected to have both conditions, the signs and symptoms related to this ovelapping and factors implicated in misdiagnose. Methods: 111 patients with an initially CIDP suspected diagnosis were studied. DNA was isolated from peripheral blood leucocytes following a standard salting-out protocol. Duplications and delections in the PMP22 gene were analysed by polymorphic DNA markers located within the chromosome 17p11.2-12, wich contains the PMP22 gene. Clinical and laboratory findings were also studied and compared within groups. Results: Among 111 patients studied, 10 (9%) were found to harbor mutations in PMP22 gene, specifically duplications in nine and delection in one. We therefore diagnosed CIDP plus CMT in four patients (3.6%), all of them with a duplicated PMP22 gene. The other six patients were diagnosed as pure CMT (5) or Hereditary Neuropathy with liability to Pressure Palsy (1), as they did not improved with the use of immunomodulatory and/or immunosupressive treatment (five cases) or were found to have alternative associated diagnosis (one patient). The other 101 patients did not show duplication nor delection in this gene, so they had CIDP. Mean age of patients with CIDP/CMT were 23.8±18.0 years and 43.6±19.3 years for patients without mutations (p=0.04). There were statistically significant difference in treatmet response between groups CIDP/CMT X CMT (p=0.008) and CIDP X CMT (p=0.00). The lack of family history and presence of other diseases and habits linked to the development of peripheral neuropathies, as diabetes mellitus and alcohol intake, for instance, as well as atypical findings in electrodiagnostic studies and nerve biopsy may have contributed to misdiagnose in the pure CMT cases. Conclusions: Some patients may develop CIDP in association with CMT and have benefit from treatment. The hereditary neuropathy may predispose to the inflammatory neuropathy as these patients tend to show this condition at younger ages. Caution should be dispensed to those patients with a suspected diagnose of CIDP who do not have the classical disease findings or do not improve with treatment, as they can have alternative etiologies for the neuropathy, among them a hereditary neuropathy as CMT disease.
Sandré, Marion. "Constances et spécificités des dysfonctionnements interactionnels dans le genre "débat politique télévisé" : une application au débat de l'entre-deux tours de l'élection présidentielle de 2007." Thesis, Montpellier 3, 2010. http://www.theses.fr/2010MON30034/document.
Повний текст джерелаThe second-round debate of presidential elections has been a significant event in French politics since 1974. The final TV debate of 2007, during which presidential candidates Ségolène Royal and Nicolas Sarkozy confronted each other, constitutes the corpus of the present study. The analysis focuses on turn-taking dysfunctions : interruption, overlapand problematic sequence. The aim of this study is to understand the function of these discursive devices in this TV political debate. First, the detailed transcription shows many turn-taking dysfunctions. Second, the analysis of the data reveals different types of interruption (intentional or not, with or without simultaneous speech, isolated or with others interruptions), different types of overlap (when two speakers begin together, when the current speaker continues speaking after the overlap or when he lets the next speaker talk) and different types of problematic sequence (when the next speaker does not answer at all or does not answer well to the first speaker). Third, each type is precisely examined. The discourse analysis demonstrates how the debater uses them to defend himself or to criticize the other person. Furthermore, as turn-taking dysfunctions are conversational insults, the discourse surrounding them is analysed as a way to save face and to build the discursive ethos. The results of this study may help the field of linguistics to understand the discursive strategies of politicians. More generally, it presents a model to analyse every type of turn-taking dysfunction. Future research might focus on other TV political debates and other discursive genres (interviews, TV programmes with politicians) so as to carry out a comparative analysis
Elmansy, Dalia F. "Computational Methods to Characterize the Etiology of Complex Diseases at Multiple Levels." Case Western Reserve University School of Graduate Studies / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1583416431321447.
Повний текст джерелаFrénoy, Antoine. "Second order selection pressures promoting the evolution and maintenance of cooperation in microbial and in silico systems." Thesis, Paris 5, 2014. http://www.theses.fr/2014PA05T050/document.
Повний текст джерелаIn the first part, I show how digital organisms adapt their genomes to encode cooperation-related genes in a more constrained way (evolvability suppression), especially using operons and overlaps also involving essential genes. In the second part, we experimentally test this view of gene overlaps as an evolutionary constraint, using both algorithmic and synthetic biology tools that we have developed. In the third part, I use agent-based simulations to show how a form of division of labour can be interpreted as a cooperative system in the light of modern evolutionary theory. In the final part, I show that the patterns of dispersal of cooperative alleles due to hitchhiking phenomena play an important role in the evolution of cooperation. The last result holds even though the hitchhiking mechanisms also applies to non-cooperative alleles, thanks to the relatedness (at cooperation-related loci) created by the local invasion of beneficial mutations (at loci not related to cooperation). The beneficial mutations form a complex and interesting equilibrium with mutational robustness, which I investigate using in silico evolution. On the whole, these results call for a more careful consideration of the second-order selection pressures in the study of social evolution, and show the necessity for more realistic models allowing to integrate such evolutionary forces. My thesis research specifically highlights the importance of the mutational landscape in the study of microbial populations and shows the increasing potential of synthetic biology as a tool to study such landscape and microbial evolution in general
Reich, Jennifer G. "Functional overlap in gene duplications of the yeast Saccharomyces cerevisiae." Thesis, 2000. http://spectrum.library.concordia.ca/1315/1/MQ59268.pdf.
Повний текст джерелаKaufman, Liana. "Identification of Non-syndromic Intellectual Disability Genes and Their Overlap with Autism." Thesis, 2011. http://hdl.handle.net/1807/29568.
Повний текст джерелаFernandes, Maria Isabel Mou Sequeira. "Anti and pro-longevity genes differentiation and overlap with age-related diseases." Master's thesis, 2015. http://hdl.handle.net/10451/20358.
Повний текст джерелаEnvelhecimento, longevidade e doenças associadas à idade (DAIs) são processos interligados e apresentam algumas semelhanças. A determinação e caracterização dos genes partilhados pelo envelhecimento ou longevidade e DAIs - genes AD - podem fornecer mais pistas acerca dos processos de regulação do envelhecimento e das DAIs, sendo este o propósito biomédico da pesquisa na área do envelhecimento. Na área da longevidade, existe já a distinção entre dois tipos de genes: anti e pró-longevidade. São considerados anti-longevidade genes cuja sobre-expressão promove a diminuição do tempo de vida; enquanto que a sobre-expressão de genes pró-longevidade está associada a um aumento do tempo de vida. No presente trabalho, foi realizado um tratamento do enviesamento presente na investigação e foram comparados os resultados das análises com e sem tratamento. O enviesamente presente na investigação resulta do conhecimento à priori que temos, por exemplo acerca de genes, e que nos conduz a uma seleção tendenciosa dos genes a estudar. Com o objetivo de definir quais os genes AD, foram realizadas análises de sobreposição sob quatro perspetivas: no genoma, no interactoma, incluindo os parceiros de primeira ordem considerando interações proteína-proteína e incluindo os genes co-expressos definidos por dados de RNA-Seq. Foram realizadas análises de algumas características e de mecanismos para os seguintes conjuntos de genes: genes AD, genes associados ao envelhecimento ou a doenças excluindo os comuns, genes anti-longevidade, genes pro-longevidade, genes associados ao envelhecimento e genes associados a doenças. Adicionalmente, para definir os genes mais comuns, foi analisada a frequência dos genes AD ao longo das DAIs. Suportado pelos resultados obtidos, a exclusão dos genes menos estudados conduz a resultados mais precisos e a definição do número mínimo de publicações pode ser um método para reduzir o enviesamento presente na investigação. O presente trabalho evidencia a associação entre envelhecimento e DAIs, assim como entre genes anti ou pró-longevidade e DAIs. Os genes envelhecimento-doença revelaram envolvimento nos principais mecanismos de envelhecimento e doenças conhecidos. As comparações do comprimento do gene, comprimento e massa da proteína, assim como da taxa de evolução molecular (dN/dS) não demonstraram nenhum padrão de distinção entre genes anti e pró-longevidade, apresentando apenas duas diferenças significativas: i) o comprimento da proteína codificada por genes anti-longevidade é o maior, na mosca da fruta e, ii) a taxa dN/dS dos genes anti-longevidade é a maior, na minhoca. Os genes envelhecimento-doenças apresentam um maior número de conexões com outros genes, o que frisa a sua importância nas redes do envelhecimento e DAIs.
Ageing, longevity and age-related diseases (ARDs) are interconnected processes and they present some similarities. The determination and characterization of common genes between ageing or longevity and ARDs - AD-genes - can provide more clues about the regulation processes involved in ageing and diseases which is the biomedical purpose of ageing research. In the longevity research, there is already a distinction between two types of genes: anti and pro-longevity. The anti-longevity genes are those whose over-expression is associated to a decrease in the life span, while the pro-longevity genes over-expression is associated to an increase in life span. In the present work, a research bias treatment and a comparison between analyses with and without this was performed. The research bias results from the à priori knowledge, for example about genes, which leads us to make a biased selection of the genes to study. In order to find AD-genes, overlap analyses were done from four perspectives: the genome, the interactome, including first order proteinprotein interactions partners, and including co-expressed genes from RNA-Seq data. Analysis of some features and functional enrichment was applied to characterize the following gene sets: AD-genes, noncommon ageing or disease genes, anti-longevity genes, pro-longevity genes, ageing genes and ARDs genes. Additionally the frequency of genes among the ARDs was analysed for AD-genes in order to define the most common genes. Supported by the obtained results, the exclusion of less studied genes leads to more accurate results and the setting of a minimum number of publications can be a method to reduce the research bias. The present work evidenced the association between ageing and ARDs, as well as the relation between anti or pro-longevity and ARDs. The AD-genes were revealed to be more involved with the main known ageing and diseases mechanisms. The comparisons of gene length, protein length and mass, as well as the molecular evolutionary (dn/ds) ratio didn't show any pattern of difference between anti and prolongevity genes, showing only two significant differences: i) the length of proteins coded by anti-longevity genes is the highest in fruit fly and, ii) the dn/ds ratio of anti-longevity genes is the highest in roundworm. The AD-genes show a higher number of connections which highlight their importance in ageing and ARDs networks.
Beinhoff, Malte. "Molecular and functional characterization of potential pathogenicity related genes from Verticillium longisporum." Doctoral thesis, 2011. http://hdl.handle.net/11858/00-1735-0000-0006-AB46-F.
Повний текст джерелаКниги з теми "Gene overlaps"
Christa, Landert, ed. "Wenn du absolut nach Amerika willst, so gehe in Gottesnamen!": Erinnerungen an den California Trail, John A. Sutter und den Goldrausch 1846-1849. 2nd ed. Zürich: Limmat-Verlag, 2011.
Знайти повний текст джерелаSiebert, Stefan, Sengupta Raj, and Alexander Tsoukas. The genetics of axial spondyloarthritis. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198755296.003.0004.
Повний текст джерелаSmith-Hicks, C. L., and S. Naidu. Rett Syndrome. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0054.
Повний текст джерелаHoldt, Lesca M., and Daniel Teupser. Genetic background of atherosclerosis and its risk factors. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199656653.003.0002.
Повний текст джерелаKan, Carol, and Ma-Li Wong. Genetics. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198789284.003.0004.
Повний текст джерелаGarcia-Pavia, Pablo, and Fernando Dominguez. Left ventricular non-compaction: genetics and embryology. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198784906.003.0362.
Повний текст джерелаLevinson, Douglas F., and Walter E. Nichols. Genetics of Depression. Edited by Dennis S. Charney, Eric J. Nestler, Pamela Sklar, and Joseph D. Buxbaum. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190681425.003.0024.
Повний текст джерелаStraaijer, Robin. The usage guide. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780198808206.003.0002.
Повний текст джерелаFranks, David D. Sex Differences in the Human Brain. Edited by Rosemary L. Hopcroft. Oxford University Press, 2018. http://dx.doi.org/10.1093/oxfordhb/9780190299323.013.6.
Повний текст джерелаOxley, Cristal, and Argyris Stringaris. Comorbidity. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780198739258.003.0022.
Повний текст джерелаЧастини книг з теми "Gene overlaps"
Harju, Tero, Ion Petre, and Grzegorz Rozenberg. "Formal Properties of Gene Assembly: Equivalence Problem for Overlap Graphs." In Aspects of Molecular Computing, 202–12. Berlin, Heidelberg: Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-540-24635-0_14.
Повний текст джерелаMakita, Naomasa. "Phenotypic Overlap of Lethal Arrhythmias Associated with Cardiac Sodium Mutations: Individual-Specific or Mutation-Specific?" In Genes and Cardiovascular Function, 185–96. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-7207-1_18.
Повний текст джерелаLi, Gang, Bing-Xue Dong, Yu-Huan Liu, Chang-Jie Li, and Li-Ping Zhang. "Gene Synthesis Method Based on Overlap Extension PCR and DNAWorks Program." In Synthetic Biology, 9–17. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-625-2_2.
Повний текст джерелаMayrhofer, Patrick, and Renate Kunert. "Cloning of Single-Chain Antibody Variants by Overlap-Extension PCR for Evaluation of Antibody Expression in Transient Gene Expression." In Methods in Molecular Biology, 57–69. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6972-2_4.
Повний текст джерелаOrwig, Marcy Leasum, and Anish Dave. "The Conflict of Genre: Disciplinary Terminology and Conceptual Overlap in the Context of the Annual Report." In Communication and Conflict Studies, 57–70. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-32746-0_4.
Повний текст джерелаZhong, Chao, Chun You, Ping Wei, and Yi-Heng Percival Zhang. "Simple Cloning by Prolonged Overlap Extension-PCR with Application to the Preparation of Large-Size Random Gene Mutagenesis Library in Escherichia coli." In Methods in Molecular Biology, 49–61. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-6343-0_4.
Повний текст джерелаNishizawa, Mikio, Tetsuya Okuyama, and Richi Nakatake. "The Natural Antisense Transcript-Targeted Regulation Technology Using Sense Oligonucleotides and Its Application." In Oligonucleotides - Overview and Applications [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.108281.
Повний текст джерелаQ. Clement, Jade. "Gene Expression Profile of HDF in SMG Partially Overlaps with That in the NASA Twins Study." In Gene Expression and Phenotypic Traits. IntechOpen, 2020. http://dx.doi.org/10.5772/intechopen.88957.
Повний текст джерелаAli, Zafar, Uzma Abdullah, and Ambrin Fatima. "Intellectual Disabilities." In Omics Technologies for Clinical Diagnosis and Gene Therapy: Medical Applications in Human Genetics, 269–82. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815079517122010019.
Повний текст джерелаRichards, Rashna Wadia. "“You’re Nobody’s Mommy”." In Cinematic TV, 111–53. Oxford University Press, 2021. http://dx.doi.org/10.1093/oso/9780190071257.003.0004.
Повний текст джерелаТези доповідей конференцій з теми "Gene overlaps"
Banerjee, Nilanjana, Vinay Varadan, Sitharthan Kamalakaran, and Angel Janevski. "Towards identification of thematic overlaps in gene sets." In 2009 IEEE International Workshop on Genomic Signal Processing and Statistics (GENSIPS). IEEE, 2009. http://dx.doi.org/10.1109/gensips.2009.5174372.
Повний текст джерелаBoudewijn, Ilse M., Alen Faiz, Katrina Steiling, Erica van der Wiel, Eef Telenga, Susan Hoonhorst, Nick ten Hacken, et al. "A nasal gene expression profile differentiates individuals with and without COPD and overlaps bronchial gene expression." In ERS International Congress 2017 abstracts. European Respiratory Society, 2017. http://dx.doi.org/10.1183/1393003.congress-2017.pa4470.
Повний текст джерелаBosacoma, Adelaida, Daniel Aguilar, Tanja Paul, Isabel Blanco, Olga Tura-Ceide, Joan Albert Barberà, and Victor I. Peinado. "The Gene Signature of Lungs from Guinea Pigs Exposed to Cigarette Smoke Overlaps with that of Human with COPD." In ERS International Congress 2020 abstracts. European Respiratory Society, 2020. http://dx.doi.org/10.1183/13993003.congress-2020.2707.
Повний текст джерелаSadler, J. Evan. "THE MOLECULAR BIOLOGY OF VON WILLEBRAND FACTOR." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643930.
Повний текст джерелаLaug, Walter E. "HETEROGENOUS EXPRESSION OF PLASMINOGEN ACTIVATOR (PA) GENES IN THE HUMAN SARCOMA CELL LINE HT1080." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644395.
Повний текст джерелаSaferali, A., J. H. Yun, S. Lee, R. Chase, P. Castaldi, and C. P. Hersh. "Gene Expression Signature of Asthma COPD Overlap." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a4555.
Повний текст джерелаBadia, Bruno de Mattos Lombardi, Roberta Ismael Lacerda Machado, Wladimir Bocca Vieira de Rezende Pinto, Igor Braga Farias, José Marcos Vieira de Albuquerque Filho, Paulo Victor Sgobbi de Souza, Márcio Luiz Escórcio Bezerra, and Acary Souza Bulle Oliveira. "Blurred Lines – Is the distinction between CIDP and CMT always clear?" In XIII Congresso Paulista de Neurologia. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1516-3180.015.
Повний текст джерелаSarbazi-Azad, Saeed, and Mohammad Saniee Abadeh. "Gene Selection for Cancer Classification from Microarray Data Using Data Overlap Measure." In 2018 25th National and 3rd International Iranian Conference on Biomedical Engineering (ICBME). IEEE, 2018. http://dx.doi.org/10.1109/icbme.2018.8703565.
Повний текст джерелаYing, Li, Lei Na, and Ma Jian. "Statistical Analysis of Gene Co-Expression Networks by Maximal Overlap Discrete Wavelet Transform." In 2009 2nd International Conference on Biomedical Engineering and Informatics. IEEE, 2009. http://dx.doi.org/10.1109/bmei.2009.5305153.
Повний текст джерелаWald, Randall, Taghi Khoshgoftaar, and David Dittman. "A New Fixed-Overlap Partitioning Algorithm for Determining Stability of Bioinformatics Gene Rankers." In 2012 Eleventh International Conference on Machine Learning and Applications (ICMLA). IEEE, 2012. http://dx.doi.org/10.1109/icmla.2012.149.
Повний текст джерелаЗвіти організацій з теми "Gene overlaps"
Horwitz, Benjamin A., and Barbara Gillian Turgeon. Fungal Iron Acquisition, Oxidative Stress and Virulence in the Cochliobolus-maize Interaction. United States Department of Agriculture, March 2012. http://dx.doi.org/10.32747/2012.7709885.bard.
Повний текст джерелаHorwitz, Benjamin, and Barbara Gillian Turgeon. Secondary Metabolites, Stress, and Signaling: Roles and Regulation of Peptides Produced by Non-ribosomal Peptide Synthetases. United States Department of Agriculture, 2005. http://dx.doi.org/10.32747/2005.7696522.bard.
Повний текст джерелаPirone, Thomas P., Benjamin Raccah, and Nor Chejanovsky. Vector Specificity in Potyvirus Transmission: Role of the Helper Component. United States Department of Agriculture, January 2003. http://dx.doi.org/10.32747/2003.7586456.bard.
Повний текст джерела