Artigos de revistas sobre o tema "High throughput sequencing (NGS)"
Crie uma referência precisa em APA, MLA, Chicago, Harvard, e outros estilos
Veja os 50 melhores artigos de revistas para estudos sobre o assunto "High throughput sequencing (NGS)".
Ao lado de cada fonte na lista de referências, há um botão "Adicionar à bibliografia". Clique e geraremos automaticamente a citação bibliográfica do trabalho escolhido no estilo de citação de que você precisa: APA, MLA, Harvard, Chicago, Vancouver, etc.
Você também pode baixar o texto completo da publicação científica em formato .pdf e ler o resumo do trabalho online se estiver presente nos metadados.
Veja os artigos de revistas das mais diversas áreas científicas e compile uma bibliografia correta.
Montmayeur, Anna M., Terry Fei Fan Ng, Alexander Schmidt, Kun Zhao, Laura Magaña, Jane Iber, Christina J. Castro et al. "High-Throughput Next-Generation Sequencing of Polioviruses". Journal of Clinical Microbiology 55, n.º 2 (7 de dezembro de 2016): 606–15. http://dx.doi.org/10.1128/jcm.02121-16.
Texto completo da fonteLi, Niannian, Kairang Jin, Yanmin Bai, Haifeng Fu, Lin Liu e Bin Liu. "Tn5 Transposase Applied in Genomics Research". International Journal of Molecular Sciences 21, n.º 21 (6 de novembro de 2020): 8329. http://dx.doi.org/10.3390/ijms21218329.
Texto completo da fonteSuravajhala, Prashanth, e Alexey Goltsov. "Three Grand Challenges in High Throughput Omics Technologies". Biomolecules 12, n.º 9 (4 de setembro de 2022): 1238. http://dx.doi.org/10.3390/biom12091238.
Texto completo da fonteSaeed, Muhammad, Zainab Jamil, Tayyab Shehzad, Syed Zia ul Hasan, Riffat Bibi, Safia Naureen Malik, Hafiz Matee-ur-Rehman e Raees Ahmed. "Role of Next Generation Sequencing (NGS) in Plant Disease Management: A Review". Journal of Applied Research in Plant Sciences 4, n.º 01 (23 de fevereiro de 2023): 512–17. http://dx.doi.org/10.38211/joarps.2023.04.01.61.
Texto completo da fonteWilliams, Gareth Haydn, Robert Paul Thatcher, Tiffany Eira Haddow, Keeda-Marie Hardisty e Marco Loddo. "Immunofocus-PD-L1 high throughput quantitative next generation sequencing assay." Journal of Clinical Oncology 38, n.º 15_suppl (20 de maio de 2020): e13521-e13521. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.e13521.
Texto completo da fonteKechin, Andrey, Viktoria Borobova, Ulyana Boyarskikh, Evgeniy Khrapov, Sergey Subbotin e Maxim Filipenko. "NGS-PrimerPlex: High-throughput primer design for multiplex polymerase chain reactions". PLOS Computational Biology 16, n.º 12 (30 de dezembro de 2020): e1008468. http://dx.doi.org/10.1371/journal.pcbi.1008468.
Texto completo da fonteWang, Qi, Lijuan Cao, Guangying Sheng, Hongjie Shen, Jing Ling, Jundan Xie, Zhenni Ma et al. "Application of High-Throughput Sequencing in the Diagnosis of Inherited Thrombocytopenia". Clinical and Applied Thrombosis/Hemostasis 24, n.º 9_suppl (13 de agosto de 2018): 94S—103S. http://dx.doi.org/10.1177/1076029618790696.
Texto completo da fonteWang, Jia-Wang, Wenxiu Zhang, Yan Zhang, Jiajia Zhou, Jing Li, Min Zhang, Shanshan Wen et al. "Reproducible and high sample throughput isomiR next-generation sequencing for cancer diagnosis." Journal of Clinical Oncology 42, n.º 16_suppl (1 de junho de 2024): e15013-e15013. http://dx.doi.org/10.1200/jco.2024.42.16_suppl.e15013.
Texto completo da fonteTripathi, Pooja, Jyotsna Singh, Jonathan A. Lal e Vijay Tripathi. "Next-Generation Sequencing: An Emerging Tool for Drug Designing". Current Pharmaceutical Design 25, n.º 31 (14 de novembro de 2019): 3350–57. http://dx.doi.org/10.2174/1381612825666190911155508.
Texto completo da fonteChae, H., S. Rhee, K. P. Nephew e S. Kim. "BioVLAB-MMIA-NGS: microRNA-mRNA integrated analysis using high-throughput sequencing data". Bioinformatics 31, n.º 2 (29 de setembro de 2014): 265–67. http://dx.doi.org/10.1093/bioinformatics/btu614.
Texto completo da fonteBeniwal, Nisha, e Baljeet Singh Saharan. "Emerging Importance of Viral Transport Media in High-Throughput Sequencing Fidelity for Genomic Analysis". Journal of Scientific Research and Reports 29, n.º 10 (7 de novembro de 2023): 99–103. http://dx.doi.org/10.9734/jsrr/2023/v29i101801.
Texto completo da fonteGerilovych, A. P., M. I. Sushko, S. S. Mandyhra, N. S. Rodyna, M. Ye Romanko, M. V. Kuchinskiy e I. O. Gerilovych. "APPLICATION OF THE NEXT GENERATION SEQUENCING IN BIOLOGY AND MEDICINE". One Health Journal 2, n.º I (6 de março de 2024): 32–44. http://dx.doi.org/10.31073/onehealthjournal2024-i-05.
Texto completo da fonteAriyadasa, Ruvini, e Nils Stein. "Advances in BAC-Based Physical Mapping and Map Integration Strategies in Plants". Journal of Biomedicine and Biotechnology 2012 (2012): 1–11. http://dx.doi.org/10.1155/2012/184854.
Texto completo da fonteSalado, Isabel, Alberto Fernández-Gil, Carles Vilà e Jennifer A. Leonard. "Automated genotyping of microsatellite loci from feces with high throughput sequences". PLOS ONE 16, n.º 10 (25 de outubro de 2021): e0258906. http://dx.doi.org/10.1371/journal.pone.0258906.
Texto completo da fonteIshiya, Koji, e Shintaroh Ueda. "MitoSuite: a graphical tool for human mitochondrial genome profiling in massive parallel sequencing". PeerJ 5 (30 de maio de 2017): e3406. http://dx.doi.org/10.7717/peerj.3406.
Texto completo da fonteZheng, Weibo, Jing Chen, Thomas G. Doak, Weibo Song e Ying Yan. "ADFinder: accurate detection of programmed DNA elimination using NGS high-throughput sequencing data". Bioinformatics 36, n.º 12 (4 de abril de 2020): 3632–36. http://dx.doi.org/10.1093/bioinformatics/btaa226.
Texto completo da fonteZubov, V. V., D. A. Chemeris, R. G. Vasilov, V. E. Kurochkin e Ya I. Alekseev. "Brief history of high-throughput nucleic acid sequencing methods." Biomics 13, n.º 1 (2021): 27–46. http://dx.doi.org/10.31301/2221-6197.bmcs.2021-4.
Texto completo da fonteBieler, Jonathan, Christian Pozzorini, Jessica Garcia, Alex C. Tuck, Morgane Macheret, Adrian Willig, Sébastien Couraud et al. "High-Throughput Nucleotide Resolution Predictions of Assay Limitations Increase the Reliability and Concordance of Clinical Tests". JCO Clinical Cancer Informatics, n.º 5 (outubro de 2021): 1085–95. http://dx.doi.org/10.1200/cci.21.00057.
Texto completo da fonteNellimarla, Srinivas, e Prasad Kesanakurti. "Next-Generation Sequencing: A Promising Tool for Vaccines and Other Biological Products". Vaccines 11, n.º 3 (23 de fevereiro de 2023): 527. http://dx.doi.org/10.3390/vaccines11030527.
Texto completo da fonteJavitt, Gail H., e Katherine Strong Carner. "Regulation of Next Generation Sequencing". Journal of Law, Medicine & Ethics 42, S1 (2014): 9–21. http://dx.doi.org/10.1111/jlme.12159.
Texto completo da fonteRoy, Denis, Sarah J. Lehnert, Clare J. Venney, Ryan Walter e Daniel D. Heath. "NGS-μsat: bioinformatics framework supporting high throughput microsatellite genotyping from next generation sequencing platforms". Conservation Genetics Resources 13, n.º 2 (11 de janeiro de 2021): 161–73. http://dx.doi.org/10.1007/s12686-020-01186-0.
Texto completo da fonteWagner, Ines, Daniel Schefzyk, Jens Pruschke, Gerhard Schoefl, Bianca Schoene, Kathrin Lang, Jan A. Hofmann et al. "OR28 High-throughput KIR sequencing by NGS: 500,000 registry samples genotyped at allelic resolution". Human Immunology 78 (setembro de 2017): 27. http://dx.doi.org/10.1016/j.humimm.2017.06.034.
Texto completo da fonteNelsen, Donald J., Rohita Sinha, Aaron J. Tyler, Jordyn Westergaard, Jamie Nutt, Mark Wissel, Steve Kleiboeker e Michelle Altrich. "268. Fungal NGS: Identification of Etiological Agents of Invasive Fungal Infection by High-throughput Sequencing". Open Forum Infectious Diseases 6, Supplement_2 (outubro de 2019): S148—S149. http://dx.doi.org/10.1093/ofid/ofz360.343.
Texto completo da fonteColabella, Claudia, Debora Casagrande Pierantoni, Laura Corte, Luca Roscini, Angela Conti, Matteo Bassetti, Carlo Tascini, Vincent Robert e Gianluigi Cardinali. "Single Strain High-Depth NGS Reveals High rDNA (ITS-LSU) Variability in the Four Prevalent Pathogenic Species of the Genus Candida". Microorganisms 9, n.º 2 (2 de fevereiro de 2021): 302. http://dx.doi.org/10.3390/microorganisms9020302.
Texto completo da fonteHassouneh, Ramzi. "Is Next-Generation Sequencing Appropriate for the Clinic?" University of Ottawa Journal of Medicine 4, n.º 2 (17 de novembro de 2014): 45–48. http://dx.doi.org/10.18192/uojm.v4i2.1075.
Texto completo da fonteLiaudanski, A. D., R. S. Shulinski, Y. A. Mishuk e L. N. Sivitskaya. "COMPARISON OF GENOTYPE PHASING METODS FOR THE HIGH THROUGHPUT SEQUENCING DATA OF CLINICAL EXOMES". Молекулярная и прикладная генетика 31 (8 de dezembro de 2021): 114–23. http://dx.doi.org/10.47612/1999-9127-2021-31-114-123.
Texto completo da fonteNowrousian, Minou. "Next-Generation Sequencing Techniques for Eukaryotic Microorganisms: Sequencing-Based Solutions to Biological Problems". Eukaryotic Cell 9, n.º 9 (2 de julho de 2010): 1300–1310. http://dx.doi.org/10.1128/ec.00123-10.
Texto completo da fonteАлексеева, Е. А., О. В. Бабенко, В. М. Козлова, Т. Л. Ушакова, Т. П. Казубская, А. С. Танас, К. И. Карандашева, В. В. Стрельников e Д. В. Залетаев. "Advantages of high throughput parallel sequencing in detecting somatic mosaicism in sporadic retinoblastoma". Nauchno-prakticheskii zhurnal «Medicinskaia genetika», n.º 6(215) (29 de junho de 2020): 6–7. http://dx.doi.org/10.25557/2073-7998.2020.06.6-7.
Texto completo da fontePark, H., S. Murthy, C. Bott, M. C. M. van Loosdrecht e K. Chandran. "Nationwide metagenome survey of anammox processes via high-throughput next generation sequencing (NGS): 2012-2013". Proceedings of the Water Environment Federation 2014, n.º 6 (1 de outubro de 2014): 2366–71. http://dx.doi.org/10.2175/193864714815942017.
Texto completo da fonteTiu, Charles Kevin, Feng Zhu, Lin-Fa Wang e Ruklanthi de Alwis. "Phage ImmunoPrecipitation Sequencing (PhIP-Seq): The Promise of High Throughput Serology". Pathogens 11, n.º 5 (11 de maio de 2022): 568. http://dx.doi.org/10.3390/pathogens11050568.
Texto completo da fonteBeck, Tyler F., James C. Mullikin e Leslie G. Biesecker. "Systematic Evaluation of Sanger Validation of Next-Generation Sequencing Variants". Clinical Chemistry 62, n.º 4 (1 de abril de 2016): 647–54. http://dx.doi.org/10.1373/clinchem.2015.249623.
Texto completo da fonteTang, Binhua, Xihan Wang e Victor X. Jin. "COPAR: A ChIP-Seq Optimal Peak Analyzer". BioMed Research International 2017 (2017): 1–4. http://dx.doi.org/10.1155/2017/5346793.
Texto completo da fonteHöing, Ann-Sophie, Alexander E. Volk e Hanno J. Bolz. "Klinische Anwendung der Hochdurchsatz-Sequenzierung (next-generation sequencing, NGS) bei der Diagnostik des Usher-Syndroms". Optometry & Contact Lenses 3, n.º 9 (30 de outubro de 2023): 308–17. http://dx.doi.org/10.54352/dozv.crqo4102.
Texto completo da fonteShetty, Omshree, Mamta Gurav, Prachi Bapat, Nupur Karnik, Gauri Wagh, Trupti Pai, Sridhar Epari e Sangeeta Desai. "Moving Next-Generation Sequencing into the Clinic". Indian Journal of Medical and Paediatric Oncology 42, n.º 03 (maio de 2021): 221–28. http://dx.doi.org/10.1055/s-0041-1732854.
Texto completo da fonteVodiasova, E. A., E. S. Chelebieva e O. N. Kuleshova. "The new technologies of high-throughput single-cell RNA sequencing". Vavilov Journal of Genetics and Breeding 23, n.º 5 (24 de agosto de 2019): 508–18. http://dx.doi.org/10.18699/vj19.520.
Texto completo da fonteBarry, Simon, Yazan Hani Mustafa, Carol McGibney, Laura Royo, Martin Higgins, Wail Mohammed, Mahzar Iqbal et al. "Impact of next generation sequencing in high grade glioma management." Journal of Clinical Oncology 42, n.º 16_suppl (1 de junho de 2024): e14031-e14031. http://dx.doi.org/10.1200/jco.2024.42.16_suppl.e14031.
Texto completo da fonteЯнова, Т. И., И. В. Канивец, С. А. Коростелев, Д. В. Пьянков, В. Ю. Удалова, К. В. Горгишели e Ю. К. Киевская. "NGS for prenatal diagnosis of fetal anomalies". Nauchno-prakticheskii zhurnal «Medicinskaia genetika», n.º 11(220) (30 de novembro de 2020): 65–66. http://dx.doi.org/10.25557/2073-7998.2020.11.65-66.
Texto completo da fonteSatam, Heena, Kandarp Joshi, Upasana Mangrolia, Sanober Waghoo, Gulnaz Zaidi, Shravani Rawool, Ritesh P. Thakare et al. "Next-Generation Sequencing Technology: Current Trends and Advancements". Biology 12, n.º 7 (13 de julho de 2023): 997. http://dx.doi.org/10.3390/biology12070997.
Texto completo da fonteCohen-Aharonov, Lyora A., Annie Rebibo-Sabbah, Adar Yaacov, Roy Z. Granit, Merav Strauss, Raul Colodner, Ori Cheshin, Shai Rosenberg e Ronen Eavri. "High throughput SARS-CoV-2 variant analysis using molecular barcodes coupled with next generation sequencing". PLOS ONE 17, n.º 6 (21 de junho de 2022): e0253404. http://dx.doi.org/10.1371/journal.pone.0253404.
Texto completo da fonteChen, Jiajia, Daqing Zhang, Wenying Yan, Dongrong Yang e Bairong Shen. "Translational Bioinformatics for Diagnostic and Prognostic Prediction of Prostate Cancer in the Next-Generation Sequencing Era". BioMed Research International 2013 (2013): 1–13. http://dx.doi.org/10.1155/2013/901578.
Texto completo da fonteGupta, Piyush Kumar, Rama Shanker Verma, Maria Frolova e Arkady Ayzenshtadt. "HIGH-THROUGHPUT SEQUENCING ANALYSIS OF MICROBIAL POPULATIONS IN ARCTIC ROCK SAMPLE". SWS Journal of EARTH AND PLANETARY SCIENCES 1, n.º 2 (1 de outubro de 2019): 29–38. http://dx.doi.org/10.35603/eps2019/issue2.03.
Texto completo da fonteCorreia, Damien, Olivia Doppelt-Azeroual, Jean-Baptiste Denis, Mathias Vandenbogaert e Valérie Caro. "MetaGenSense : A web application for analysis and visualization of high throughput sequencing metagenomic data". F1000Research 4 (2 de abril de 2015): 86. http://dx.doi.org/10.12688/f1000research.6139.1.
Texto completo da fonteCorreia, Damien, Olivia Doppelt-Azeroual, Jean-Baptiste Denis, Mathias Vandenbogaert e Valérie Caro. "MetaGenSense: A web-application for analysis and exploration of high throughput sequencing metagenomic data". F1000Research 4 (22 de agosto de 2016): 86. http://dx.doi.org/10.12688/f1000research.6139.2.
Texto completo da fonteCorreia, Damien, Olivia Doppelt-Azeroual, Jean-Baptiste Denis, Mathias Vandenbogaert e Valérie Caro. "MetaGenSense: A web-application for analysis and exploration of high throughput sequencing metagenomic data". F1000Research 4 (1 de dezembro de 2016): 86. http://dx.doi.org/10.12688/f1000research.6139.3.
Texto completo da fonteMa, Zeqiang, Jason Gottwals, Hao Ho, Kristina J. Fasig, Heather Rietz, Taylor Hartley, Vladimir Kravstov et al. "Clinical Utility of High-Throughput and Complimentary Genomic Tumor Profiling in Hematologic Malignancies". Blood 126, n.º 23 (3 de dezembro de 2015): 1388. http://dx.doi.org/10.1182/blood.v126.23.1388.1388.
Texto completo da fonteWesołowski, Wojciech, Beata Domnicz, Joanna Augustynowicz e Marek Szklarczyk. "VCF2CAPS–A high-throughput CAPS marker design from VCF files and its test-use on a genotyping-by-sequencing (GBS) dataset". PLOS Computational Biology 17, n.º 5 (20 de maio de 2021): e1008980. http://dx.doi.org/10.1371/journal.pcbi.1008980.
Texto completo da fonteThomson, Emma, Camilla L. C. Ip, Anjna Badhan, Mette T. Christiansen, Walt Adamson, M. Azim Ansari, David Bibby et al. "Comparison of Next-Generation Sequencing Technologies for Comprehensive Assessment of Full-Length Hepatitis C Viral Genomes". Journal of Clinical Microbiology 54, n.º 10 (6 de julho de 2016): 2470–84. http://dx.doi.org/10.1128/jcm.00330-16.
Texto completo da fonteKhan, Anwar, Nagehan Pakasticali, Omar Fathalla, Taiga Nishihori e Mohammad O. Hussaini. "Retrospective Analysis of Minimal Residual Disease Testing By High Throughput Immunosequencing Versus High Sensitivity Flow Cytometry in Multiple Myeloma". Blood 138, Supplement 1 (5 de novembro de 2021): 1625. http://dx.doi.org/10.1182/blood-2021-154418.
Texto completo da fonteHarris, Marian, Donna S. Neuberg, Jianbiao Zheng, Malek Faham, Stephen E. Sallan e Lewis B. Silverman. "Minimal Residual Disease Detection Using High-Throughput Sequencing Predicts Clinical Outcome in Patients with Pediatric B-Lineage Acute Lymphoblastic Leukemia". Blood 124, n.º 21 (6 de dezembro de 2014): 2391. http://dx.doi.org/10.1182/blood.v124.21.2391.2391.
Texto completo da fonteTierno, Domenico, Gabriele Grassi, Serena Scomersi, Marina Bortul, Daniele Generali, Fabrizio Zanconati e Bruna Scaggiante. "Next-Generation Sequencing and Triple-Negative Breast Cancer: Insights and Applications". International Journal of Molecular Sciences 24, n.º 11 (2 de junho de 2023): 9688. http://dx.doi.org/10.3390/ijms24119688.
Texto completo da fonte