Gotowa bibliografia na temat „Direct sequencing”
Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych
Spis treści
Zobacz listy aktualnych artykułów, książek, rozpraw, streszczeń i innych źródeł naukowych na temat „Direct sequencing”.
Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.
Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.
Artykuły w czasopismach na temat "Direct sequencing"
Ozsolak, Fatih, Adam R. Platt, Dan R. Jones, Jeffrey G. Reifenberger, Lauryn E. Sass, Peter McInerney, John F. Thompson, Jayson Bowers, Mirna Jarosz i Patrice M. Milos. "Direct RNA sequencing". Nature 461, nr 7265 (23.09.2009): 814–18. http://dx.doi.org/10.1038/nature08390.
Pełny tekst źródłaLinder, Jodell E., Tatyana E. Plachco, Romina Libster i E. Kathryn Miller. "Sequencing human rhinoviruses: Direct sequencing versus plasmid cloning". Journal of Virological Methods 211 (styczeń 2015): 64–69. http://dx.doi.org/10.1016/j.jviromet.2014.09.020.
Pełny tekst źródłaChalapati, Sachin, Conor A. Crosbie, Dixita Limbachiya i Nimesh Pinnamaneni. "Direct oligonucleotide sequencing with nanopores". Open Research Europe 1 (24.08.2021): 47. http://dx.doi.org/10.12688/openreseurope.13578.2.
Pełny tekst źródłaChalapati, Sachin, Conor A. Crosbie, Dixita Limbachiya i Nimesh Pinnamaneni. "Direct oligonucleotide sequencing with nanopores". Open Research Europe 1 (12.05.2021): 47. http://dx.doi.org/10.12688/openreseurope.13578.1.
Pełny tekst źródłaRudi, Heidi, Knut‐Erik Gylder, Odd Arne Rognli i Knut Rudi. "Direct Haplotype‐Specific DNA Sequencing". Preparative Biochemistry and Biotechnology 36, nr 3 (wrzesień 2006): 253–57. http://dx.doi.org/10.1080/10826060600716687.
Pełny tekst źródłaZhang, Jinyue, Shuanghong Yan, Le Chang, Weiming Guo, Yuqin Wang, Yu Wang, Panke Zhang, Hong-Yuan Chen i Shuo Huang. "Direct microRNA Sequencing Using Nanopore-Induced Phase-Shift Sequencing". iScience 23, nr 3 (marzec 2020): 100916. http://dx.doi.org/10.1016/j.isci.2020.100916.
Pełny tekst źródłaKilger, Christian, Matthias Krings, Hendrik Poinar i Svante Pääbo. "“Colony Sequencing”: Direct Sequencing of Plasmid DNA from Bacterial Colonies". BioTechniques 22, nr 3 (marzec 1997): 412–18. http://dx.doi.org/10.2144/97223bm08.
Pełny tekst źródłaPetry, H., K. Pekrun, K. Wäse, I. Schedel, W. Lüke i G. Hunsmann. "Direct sequencing versus cloned amplicon sequencing in HIV-1 diagnosis". Experientia 52, nr 4 (kwiecień 1996): 303–4. http://dx.doi.org/10.1007/bf01919520.
Pełny tekst źródłaObata, Hiroko, Tatsuya Tanaka, Tsuneko Fujii, Chikako Sasho, Yukihiro Yamaguchi i Keiichiro Suzuki. "Dye Terminator Re-cycle-sequencing Method: Phage Plaque Direct Sequencing". Analytical Biochemistry 297, nr 1 (październik 2001): 102–5. http://dx.doi.org/10.1006/abio.2001.5328.
Pełny tekst źródłaZhang, Jinyue. "Direct MicroRNA Sequencing using Nanopore Induced Phase-Shift Sequencing (NIPSS)". Biophysical Journal 118, nr 3 (luty 2020): 475a—476a. http://dx.doi.org/10.1016/j.bpj.2019.11.2638.
Pełny tekst źródłaRozprawy doktorskie na temat "Direct sequencing"
Fillion, Bergeron Marianne. "Plasmid isolation and purification by electrofiltration and comparison of different direct colony sequencing methods and PCR-based sequencing methods". Thesis, University of Ottawa (Canada), 2002. http://hdl.handle.net/10393/6050.
Pełny tekst źródła梁秀敏 i Sau-man Leung. "Direct detection of rifampin-resistant mycobacterium tuberculosis in clinical specimens by DNA sequencing". Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2001. http://hub.hku.hk/bib/B31970102.
Pełny tekst źródłaLeung, Sau-man. "Direct detection of rifampin-resistant mycobacterium tuberculosis in clinical specimens by DNA sequencing". Hong Kong : University of Hong Kong, 2001. http://sunzi.lib.hku.hk/hkuto/record.jsp?B2329498X.
Pełny tekst źródłaOtten, Nathalie. "DNA of bovine papillomavirus type 1 and 2 in equine sarcoids : PCR detection and direct sequencing /". [S.l.] : [s.n.], 1992. http://www.ub.unibe.ch/content/bibliotheken_sammlungen/sondersammlungen/dissen_bestellformular/index_ger.html.
Pełny tekst źródłaRocha, Ana Laís Bignotto da. "Sequenciamento direto dos genes SIX3, SHH, TGIF1, ZIC2 e array-CGH no estudo de pacientes com holoprosencefalia". Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/61/61132/tde-12112013-150520/.
Pełny tekst źródłaObjective: Analyze through direct sequencing technique the presence of molecular changes on the genes SHH, SIX3, ZIC2 and TGIF1 on individuals with clinical diagnosis of HPE. Analyze through array-CGH technique the presence of molecular changes on individuals with clinical diagnosis of HPE previously submitted to the direct sequencing analyzes. Local: Genetics and Human Cytogenetics Laboratory, HRAC/USP, Bauru-SP. Methods: Were selected 50 individuals from both genders with ages between 03 months and 50 years clinically diagnosed with HPE. Everyone was analyzed through the direct sequencing technique for the genes SHH and TGIF1 completely and for the genes ZIC2 and SIX3 partially. From those individuals which did not have shown changes on the direct sequencing technique, eight individuals with more severe phenotype were selected to the analysis through array-CGH. Results an Discussion: Were analyzed 50 individuals through the technique of direct sequencing of the genes SHH and TGIF1, were found two pathogenic variants in the analysis of SHH gene, in the case 1, the variant p.G24P was identified, and in the case 2 was identified the variant c.1031delC. On the TGIF1 gene were found five polymorphisms already described on the literature. Was identified a new silent variant on the exon 1 of the ZIC2 gene p. Q46Q(c.431G>A) and a polymorphism already described in the literature in two individuals on the gene SIX3. The analysis through array-CGH revealed the presence of one microdeletion in the case 37, of 1,5 Mb on the region 17p12 between the genomic positions 14,052,279-15,102,307. The same deletion was detected in the mother, though this region was never associated to the HPE. Conclusion: The direct sequencing technique is a very important tool for the molecular diagnosis of the HPE, and the direct sequencing standardization for the genes ZIC2 and SIX3 might help in more precise diagnostics on HRAC/USP future studies. The employ of new techniques such as array-CGH may indicate new relations between chromosomal regions and the multiple hit involved in the development of HPE.
Vander, Wiede Jamie. "Direct, hands-on or inquiry instruction a study of instructional sequencing and motivation in the science classroom". Master's thesis, University of Central Florida, 2011. http://digital.library.ucf.edu/cdm/ref/collection/ETD/id/5073.
Pełny tekst źródłaID: 030423060; System requirements: World Wide Web browser and PDF reader.; Mode of access: World Wide Web.; Thesis (M.A.)--University of Central Florida, 2011.; Includes bibliographical references (p. 42-48).
M.A.
Masters
Teaching, Learning and Leadership
Education
Applied Learning and Instrucation
Koziol, Adam. "Application of Direct-sequencing Peptide Proteomics to the Characterization of Antagonistic (Endogenous and Exogenous) Proteins in Cereal Grains". Thèse, Université d'Ottawa / University of Ottawa, 2013. http://hdl.handle.net/10393/23853.
Pełny tekst źródłaNguyen, Thuy. "Ultra-deep sequencing applications in virology research". Electronic Thesis or Diss., Sorbonne université, 2018. http://www.theses.fr/2018SORUS282.
Pełny tekst źródłaThe two RNA viruses HIV and HCV are getting a lot of public health concerns because both of them have overlapping risk factors for transmission through direct blood and sexual contacts. Furthermore, HIV and HCV infections are the leading cause of mortality and morbidity globally due to related diseases. However, with the introduction of antiretroviral therapy (ART) for the treatment of HIV infection and direct-acting antivirals (DAAs) for the treatment of HCV infection, patients infected by these viruses are witnessing significant improvement in their quality of life. However, the high replication rate and the lack of error correction mechanism of these viruses result in a diverse viral population referred to as quasispecies. Under drug- selective pressure, the viral quasispecies select resistance variants against corresponding drug and render the therapy ineffective especially in cases an appropriate treatment monitoring is not ensured.To reserve a wide range of possibilities for a life-long ART in HIV-infected patients and in parallel to reduce cost for treatment of both HIV and HCV infection, research focusing on detection, surveillance and transmission of resistance mutations is fundamental to prevent treatment failure on antivirals. In this PhD, we employed the ultra-deep sequencing (UDS) or next-generation sequencing (NGS) technologies to look for minority resistant variants (MiRVs) which are conventionally considered to represent less than 15%-25% of viral population and undetectable by Sanger sequencing. The presence of MiRVs at baseline is possibly responsible for the treatment failure and their presence at failure may limit options for subsequent therapies. In this PhD, we evaluated the prevalence and clinical impact of MiRVs on integrase gene in HIV-infected patients failing an integrase inhibitor containing regimen. We also evaluated the impact of MiRVs in HCV genotype 3 and genotype 4-infected patients failing DAAs. Furthermore, we used the UDS technique to identify and characterize the HCV transmission networks among a key population of men having sex with men either co-infected with HIV or at high risk of HIV acquisition. We also discovered several cases of mixed HCV genotype infections in this population probably for their high risk of multiple HCV exposures. The advantages of UDS in virology research and the applicability of this technique in clinic have been questioned and verified throughout multiple types of projects in this PhD. UDS has not been conclusively established to be more interesting and beneficial than Sanger sequencing in prevention of treatment failure in patients infected by HIV or HCV and in identifying the viral transmission networks at large scale if taking into account the experiment cost and time for data analysis. However, the dynamic development of UDS technologies and the continuing attempts in optimizing analysis procedures display a promising role of UDS. And the applicability of UDS in clinical practice still needs to be elucidated in different kinds of research projects
Engström, Erik. "Direct poly(A) RNA nanopore sequencing on the freshwater duck mussel Anodonta anatina following exposure to copper : A pilot study". Thesis, Högskolan i Skövde, Institutionen för biovetenskap, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-17508.
Pełny tekst źródłaBusson, Laurent. "Evolution of direct diagnostic techniques in Virology; analytical performances and clinical input". Doctoral thesis, Universite Libre de Bruxelles, 2020. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/313391.
Pełny tekst źródłaDoctorat en Sciences médicales (Médecine)
info:eu-repo/semantics/nonPublished
Książki na temat "Direct sequencing"
1937-, Jost J. P., red. A laboratory guide to genomic sequencing: The direct sequencing of native uncloned DNA. Basel: Birkhäuser, 1987.
Znajdź pełny tekst źródłaJost i Saluz. Laboratory Guide to Genomic Sequencing: The Direct Sequencing of Native Uncloned DNA. Birkhauser Verlag, 2013.
Znajdź pełny tekst źródłaJost i Saluz. A Laboratory Guide to Genomic Sequencing: The Direct Sequencing of Native Uncloned DNA. Birkhäuser, 2011.
Znajdź pełny tekst źródłaJost, J. P., i H. P. Saluz. A Laboratory Guide to Genomic Sequencing: The Direct Sequencing of Native Uncloned DNA (Biomethods). Birkhauser, 1988.
Znajdź pełny tekst źródłaCaillaud, Catherine, i Frédéric Sedel. Neuronal Ceroid Lipofuscinoses. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0059.
Pełny tekst źródłaEllingboe, James. The PCR Technique : DNA Sequencing. Eaton Publishing Company/Biotechniques Books, 1992.
Znajdź pełny tekst źródłaGraves, Tracey. Neurogenetic disease. Redaktorzy Patrick Davey i David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0223.
Pełny tekst źródłaHarms, Matthew B., i Timothy M. Miller. Amyotrophic Lateral Sclerosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0027.
Pełny tekst źródłaVaheri, Antti, James N. Mills, Christina F. Spiropoulou i Brian Hjelle. Hantaviruses. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198570028.003.0035.
Pełny tekst źródłaCzęści książek na temat "Direct sequencing"
Schieltz, David M., i John R. Yates. "Direct Identification of Proteins in Ultracomplex Mixtures". W Protein Sequencing Protocols, 235–45. Totowa, NJ: Humana Press, 2003. http://dx.doi.org/10.1385/1-59259-342-9:235.
Pełny tekst źródłaRay, Kunal, Arijit Mukhopadhyay i Mainak Sengupta. "Gene Discovery by Direct Genome Sequencing". W Gene Discovery for Disease Models, 215–33. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9780470933947.ch11.
Pełny tekst źródłaMazars, Georges-Raoul, i Charles Theillet. "Direct Sequencing by Thermal Asymmetric PCR". W PCR Protocols, 355–59. Totowa, NJ: Humana Press, 2003. http://dx.doi.org/10.1007/978-1-4612-0055-0_52.
Pełny tekst źródłaSmith, Linda K. "HLA Typing by Direct DNA Sequencing". W Methods in Molecular Biology™, 67–86. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-842-9_5.
Pełny tekst źródłaHong, Tao. "Direct Nucleotide Sequencing for Amplification Product Identification". W Advanced Techniques in Diagnostic Microbiology, 389–402. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-33900-9_19.
Pełny tekst źródłaDžunková, Mária. "Flow Cytometry and Direct Sequencing of Viruses". W The Human Virome, 3–14. New York, NY: Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-8682-8_1.
Pełny tekst źródłaHong, Tao. "Direct Nucleotide Sequencing for Amplification Product Identification". W Advanced Techniques in Diagnostic Microbiology, 383–95. Boston, MA: Springer US, 2012. http://dx.doi.org/10.1007/978-1-4614-3970-7_22.
Pełny tekst źródłaKrautwurst, Sebastian, Ronald Dijkman, Volker Thiel, Andi Krumbholz i Manja Marz. "Direct RNA Sequencing for Complete Viral Genomes". W Virus Bioinformatics, 35–50. Boca Raton: Chapman and Hall/CRC, 2021. http://dx.doi.org/10.1201/9781003097679-3.
Pełny tekst źródłaHansen, C., M. Jørgensen, M. Bévort, R. Hummel, M. Løfgreen, N. Pallisgaard i H. Leffers. "Direct Automated Sequencing of DDRT-PCR Fragments". W Fingerprinting Methods Based on Arbitrarily Primed PCR, 345–51. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-60441-6_35.
Pełny tekst źródłaGyllensten, Ulf. "Direct Sequencing of In Vitro Amplified DNA". W PCR Technology, 45–60. London: Palgrave Macmillan UK, 1989. http://dx.doi.org/10.1007/978-1-349-20235-5_5.
Pełny tekst źródłaStreszczenia konferencji na temat "Direct sequencing"
Heath, Samuel A., Franco P. Preparata i Joel Young. "Sequencing by hybridization using direct and reverse cooperating spectra". W the sixth annual international conference. New York, New York, USA: ACM Press, 2002. http://dx.doi.org/10.1145/565196.565220.
Pełny tekst źródłaYanagi, Itaru, Rena Akahori, Tomio Iwasaki, Yusuke Goto, Kazuma Matsui, Yoshikazu Nara, Naomi Manri, Mayu Aoki, Takahide Yokoi i Ken-ichi Takeda. "Fabrication and analysis of SiN nanopores for direct DNA sequencing". W 2015 IEEE International Electron Devices Meeting (IEDM). IEEE, 2015. http://dx.doi.org/10.1109/iedm.2015.7409692.
Pełny tekst źródłaCox, M., S. Carney, L. Hoyles, S. Roy, R. Williams, J. Breuer, V. Chalker i M. Moffatt. "Legionella Pneumophila Typing by Direct Sequencing of Clinical and Environmental Samples". W American Thoracic Society 2020 International Conference, May 15-20, 2020 - Philadelphia, PA. American Thoracic Society, 2020. http://dx.doi.org/10.1164/ajrccm-conference.2020.201.1_meetingabstracts.a2121.
Pełny tekst źródłaSchmitt, Michael W., Jesse J. Salk, Edward J. Fox, Justin R. Pritchard, J. Graeme Hodgson, Victor M. Rivera, Pamela S. Becker, Jerald P. Radich i Lawrence A. Loeb. "Abstract 2395: Direct assessment of sequence heterogeneity in human cancers by Duplex Sequencing". W Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-2395.
Pełny tekst źródłaKolodziejski, Noah J., Rajan Gurjar, Karthik Vishwanath i David Wolf. "Tip-Enhanced Raman Spectroscopy: Focusing in on a Direct Sequencing Method for Oxidized DNA". W Biomedical Optics. Washington, D.C.: OSA, 2014. http://dx.doi.org/10.1364/biomed.2014.bt3a.29.
Pełny tekst źródłaYanagi, Itaru, Takeshi Oura, Takanobu Haga, Masahiko Ando, Jiro Yamamoto, Toshiyuki Mine, Takeshi Ishida i in. "A novel side-gated ultrathin-channel nanopore FET (SGNAFET) sensor for direct DNA sequencing". W 2013 IEEE International Electron Devices Meeting (IEDM). IEEE, 2013. http://dx.doi.org/10.1109/iedm.2013.6724629.
Pełny tekst źródłaSianipar, Nesti Fronika, Reflinur, Muhammad Dzulkifly Ashan, Khoirunnisa Assidqi, Dwityantari Widyaningrum i Ragapadmi Purnamaningsih. "Direct verification of bogor superior mutant (Typhonium flagelliforme) using RAPD marker techniques and sequencing analysis". W THE 8TH INTERNATIONAL CONFERENCE AND WORKSHOP ON BASIC AND APPLIED SCIENCE (ICOWOBAS) 2021. AIP Publishing, 2023. http://dx.doi.org/10.1063/5.0104057.
Pełny tekst źródłaKarunyakorn, Jirachote, Naruemon Pratanwanich, Monnat Pongpanich i Pornchai Kaewsapsak. "A Computational Workflow for Estimation of Short RNA Polyadenylation using Direct RNA Nanopore Sequencing with Polyuridylation". W 2022 19th International Joint Conference on Computer Science and Software Engineering (JCSSE). IEEE, 2022. http://dx.doi.org/10.1109/jcsse54890.2022.9836262.
Pełny tekst źródłaFlusberg, Benjamin, Dale Webster, Kevin Travers, Eric Olivares, Jonas Korlach i Stephen Turner. "Abstract 1154: Direct detection of DNA methylation and mutagenic damage through single-molecule, real-time (SMRTTM) DNA sequencing". W Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-1154.
Pełny tekst źródłaShekhar, Sudip, Rajesh Inti, James Jaussi, Tzu-Chien Hsueh i Bryan Casper. "A 1.2–5Gb/s 1.4–2pJ/b serial link in 22nm CMOS with a direct data-sequencing blind oversampling CDR". W 2015 Symposium on VLSI Circuits. IEEE, 2015. http://dx.doi.org/10.1109/vlsic.2015.7231319.
Pełny tekst źródłaRaporty organizacyjne na temat "Direct sequencing"
Rhodes, C. K. Human genome sequencing with direct x-ray holographic imaging. Office of Scientific and Technical Information (OSTI), czerwiec 1993. http://dx.doi.org/10.2172/6288788.
Pełny tekst źródłaRhodes, C. K. Human genome sequencing with direct x-ray holographic imaging. Final report. Office of Scientific and Technical Information (OSTI), czerwiec 1993. http://dx.doi.org/10.2172/10168190.
Pełny tekst źródłaGelb, Jr., Jack, Yoram Weisman, Brian Ladman i Rosie Meir. Identification of Avian Infectious Brochitis Virus Variant Serotypes and Subtypes by PCR Product Cycle Sequencing for the Rational Selection of Effective Vaccines. United States Department of Agriculture, grudzień 2003. http://dx.doi.org/10.32747/2003.7586470.bard.
Pełny tekst źródłaMehmood, Hamid, Surya Karthik Mukkavilli, Ingmar Weber, Atsushi Koshio, Chinaporn Meechaiya, Thanapon Piman, Kenneth Mubea, Cecilia Tortajada, Kimberly Mahadeo i Danielle Liao. Strategic Foresight to Applications of Artificial Intelligence to Achieve Water-related Sustainable Development Goals. United Nations University Institute for Water, Environment and Health, kwiecień 2020. http://dx.doi.org/10.53328/lotc2968.
Pełny tekst źródłaFahima, Tzion, i Jorge Dubcovsky. Map-based cloning of the novel stripe rust resistance gene YrG303 and its use to engineer 1B chromosome with multiple beneficial traits. United States Department of Agriculture, styczeń 2013. http://dx.doi.org/10.32747/2013.7598147.bard.
Pełny tekst źródłaTang, Jiqin, Gong Zhang, Jinxiao Xing, Ying Yu i Tao Han. Network Meta-analysis of Heat-clearing and Detoxifying Oral Liquid of Chinese Medicines in Treatment of Children’s Hand-foot-mouth Disease:a protocol for systematic review. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, styczeń 2022. http://dx.doi.org/10.37766/inplasy2022.1.0032.
Pełny tekst źródłaDubcovsky, Jorge, Tzion Fahima, Ann Blechl i Phillip San Miguel. Validation of a candidate gene for increased grain protein content in wheat. United States Department of Agriculture, styczeń 2007. http://dx.doi.org/10.32747/2007.7695857.bard.
Pełny tekst źródłaBercovier, Herve, i Ronald P. Hedrick. Diagnostic, eco-epidemiology and control of KHV, a new viral pathogen of koi and common carp. United States Department of Agriculture, grudzień 2007. http://dx.doi.org/10.32747/2007.7695593.bard.
Pełny tekst źródłaMawassi, Munir, i Valerian V. Dolja. Role of the viral AlkB homologs in RNA repair. United States Department of Agriculture, czerwiec 2014. http://dx.doi.org/10.32747/2014.7594396.bard.
Pełny tekst źródłaLevisohn, Sharon, Maricarmen Garcia, David Yogev i Stanley Kleven. Targeted Molecular Typing of Pathogenic Avian Mycoplasmas. United States Department of Agriculture, styczeń 2006. http://dx.doi.org/10.32747/2006.7695853.bard.
Pełny tekst źródła