Journal articles on the topic 'High throughput sequencing (NGS)'
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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, no. 2 (December 7, 2016): 606–15. http://dx.doi.org/10.1128/jcm.02121-16.
Full textLi, Niannian, Kairang Jin, Yanmin Bai, Haifeng Fu, Lin Liu, and Bin Liu. "Tn5 Transposase Applied in Genomics Research." International Journal of Molecular Sciences 21, no. 21 (November 6, 2020): 8329. http://dx.doi.org/10.3390/ijms21218329.
Full textSuravajhala, Prashanth, and Alexey Goltsov. "Three Grand Challenges in High Throughput Omics Technologies." Biomolecules 12, no. 9 (September 4, 2022): 1238. http://dx.doi.org/10.3390/biom12091238.
Full textSaeed, Muhammad, Zainab Jamil, Tayyab Shehzad, Syed Zia ul Hasan, Riffat Bibi, Safia Naureen Malik, Hafiz Matee-ur-Rehman, and Raees Ahmed. "Role of Next Generation Sequencing (NGS) in Plant Disease Management: A Review." Journal of Applied Research in Plant Sciences 4, no. 01 (February 23, 2023): 512–17. http://dx.doi.org/10.38211/joarps.2023.04.01.61.
Full textWilliams, Gareth Haydn, Robert Paul Thatcher, Tiffany Eira Haddow, Keeda-Marie Hardisty, and Marco Loddo. "Immunofocus-PD-L1 high throughput quantitative next generation sequencing assay." Journal of Clinical Oncology 38, no. 15_suppl (May 20, 2020): e13521-e13521. http://dx.doi.org/10.1200/jco.2020.38.15_suppl.e13521.
Full textKechin, Andrey, Viktoria Borobova, Ulyana Boyarskikh, Evgeniy Khrapov, Sergey Subbotin, and Maxim Filipenko. "NGS-PrimerPlex: High-throughput primer design for multiplex polymerase chain reactions." PLOS Computational Biology 16, no. 12 (December 30, 2020): e1008468. http://dx.doi.org/10.1371/journal.pcbi.1008468.
Full textWang, 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, no. 9_suppl (August 13, 2018): 94S—103S. http://dx.doi.org/10.1177/1076029618790696.
Full textWang, 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, no. 16_suppl (June 1, 2024): e15013-e15013. http://dx.doi.org/10.1200/jco.2024.42.16_suppl.e15013.
Full textTripathi, Pooja, Jyotsna Singh, Jonathan A. Lal, and Vijay Tripathi. "Next-Generation Sequencing: An Emerging Tool for Drug Designing." Current Pharmaceutical Design 25, no. 31 (November 14, 2019): 3350–57. http://dx.doi.org/10.2174/1381612825666190911155508.
Full textChae, H., S. Rhee, K. P. Nephew, and S. Kim. "BioVLAB-MMIA-NGS: microRNA-mRNA integrated analysis using high-throughput sequencing data." Bioinformatics 31, no. 2 (September 29, 2014): 265–67. http://dx.doi.org/10.1093/bioinformatics/btu614.
Full textBeniwal, Nisha, and Baljeet Singh Saharan. "Emerging Importance of Viral Transport Media in High-Throughput Sequencing Fidelity for Genomic Analysis." Journal of Scientific Research and Reports 29, no. 10 (November 7, 2023): 99–103. http://dx.doi.org/10.9734/jsrr/2023/v29i101801.
Full textGerilovych, A. P., M. I. Sushko, S. S. Mandyhra, N. S. Rodyna, M. Ye Romanko, M. V. Kuchinskiy, and I. O. Gerilovych. "APPLICATION OF THE NEXT GENERATION SEQUENCING IN BIOLOGY AND MEDICINE." One Health Journal 2, no. I (March 6, 2024): 32–44. http://dx.doi.org/10.31073/onehealthjournal2024-i-05.
Full textAriyadasa, Ruvini, and 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.
Full textSalado, Isabel, Alberto Fernández-Gil, Carles Vilà, and Jennifer A. Leonard. "Automated genotyping of microsatellite loci from feces with high throughput sequences." PLOS ONE 16, no. 10 (October 25, 2021): e0258906. http://dx.doi.org/10.1371/journal.pone.0258906.
Full textIshiya, Koji, and Shintaroh Ueda. "MitoSuite: a graphical tool for human mitochondrial genome profiling in massive parallel sequencing." PeerJ 5 (May 30, 2017): e3406. http://dx.doi.org/10.7717/peerj.3406.
Full textZheng, Weibo, Jing Chen, Thomas G. Doak, Weibo Song, and Ying Yan. "ADFinder: accurate detection of programmed DNA elimination using NGS high-throughput sequencing data." Bioinformatics 36, no. 12 (April 4, 2020): 3632–36. http://dx.doi.org/10.1093/bioinformatics/btaa226.
Full textZubov, V. V., D. A. Chemeris, R. G. Vasilov, V. E. Kurochkin, and Ya I. Alekseev. "Brief history of high-throughput nucleic acid sequencing methods." Biomics 13, no. 1 (2021): 27–46. http://dx.doi.org/10.31301/2221-6197.bmcs.2021-4.
Full textBieler, 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, no. 5 (October 2021): 1085–95. http://dx.doi.org/10.1200/cci.21.00057.
Full textNellimarla, Srinivas, and Prasad Kesanakurti. "Next-Generation Sequencing: A Promising Tool for Vaccines and Other Biological Products." Vaccines 11, no. 3 (February 23, 2023): 527. http://dx.doi.org/10.3390/vaccines11030527.
Full textJavitt, Gail H., and 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.
Full textRoy, Denis, Sarah J. Lehnert, Clare J. Venney, Ryan Walter, and Daniel D. Heath. "NGS-μsat: bioinformatics framework supporting high throughput microsatellite genotyping from next generation sequencing platforms." Conservation Genetics Resources 13, no. 2 (January 11, 2021): 161–73. http://dx.doi.org/10.1007/s12686-020-01186-0.
Full textWagner, 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 (September 2017): 27. http://dx.doi.org/10.1016/j.humimm.2017.06.034.
Full textNelsen, Donald J., Rohita Sinha, Aaron J. Tyler, Jordyn Westergaard, Jamie Nutt, Mark Wissel, Steve Kleiboeker, and Michelle Altrich. "268. Fungal NGS: Identification of Etiological Agents of Invasive Fungal Infection by High-throughput Sequencing." Open Forum Infectious Diseases 6, Supplement_2 (October 2019): S148—S149. http://dx.doi.org/10.1093/ofid/ofz360.343.
Full textColabella, Claudia, Debora Casagrande Pierantoni, Laura Corte, Luca Roscini, Angela Conti, Matteo Bassetti, Carlo Tascini, Vincent Robert, and 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, no. 2 (February 2, 2021): 302. http://dx.doi.org/10.3390/microorganisms9020302.
Full textHassouneh, Ramzi. "Is Next-Generation Sequencing Appropriate for the Clinic?" University of Ottawa Journal of Medicine 4, no. 2 (November 17, 2014): 45–48. http://dx.doi.org/10.18192/uojm.v4i2.1075.
Full textLiaudanski, A. D., R. S. Shulinski, Y. A. Mishuk, and L. N. Sivitskaya. "COMPARISON OF GENOTYPE PHASING METODS FOR THE HIGH THROUGHPUT SEQUENCING DATA OF CLINICAL EXOMES." Молекулярная и прикладная генетика 31 (December 8, 2021): 114–23. http://dx.doi.org/10.47612/1999-9127-2021-31-114-123.
Full textNowrousian, Minou. "Next-Generation Sequencing Techniques for Eukaryotic Microorganisms: Sequencing-Based Solutions to Biological Problems." Eukaryotic Cell 9, no. 9 (July 2, 2010): 1300–1310. http://dx.doi.org/10.1128/ec.00123-10.
Full textАлексеева, Е. А., О. В. Бабенко, В. М. Козлова, Т. Л. Ушакова, Т. П. Казубская, А. С. Танас, К. И. Карандашева, В. В. Стрельников, and Д. В. Залетаев. "Advantages of high throughput parallel sequencing in detecting somatic mosaicism in sporadic retinoblastoma." Nauchno-prakticheskii zhurnal «Medicinskaia genetika», no. 6(215) (June 29, 2020): 6–7. http://dx.doi.org/10.25557/2073-7998.2020.06.6-7.
Full textPark, H., S. Murthy, C. Bott, M. C. M. van Loosdrecht, and K. Chandran. "Nationwide metagenome survey of anammox processes via high-throughput next generation sequencing (NGS): 2012-2013." Proceedings of the Water Environment Federation 2014, no. 6 (October 1, 2014): 2366–71. http://dx.doi.org/10.2175/193864714815942017.
Full textTiu, Charles Kevin, Feng Zhu, Lin-Fa Wang, and Ruklanthi de Alwis. "Phage ImmunoPrecipitation Sequencing (PhIP-Seq): The Promise of High Throughput Serology." Pathogens 11, no. 5 (May 11, 2022): 568. http://dx.doi.org/10.3390/pathogens11050568.
Full textBeck, Tyler F., James C. Mullikin, and Leslie G. Biesecker. "Systematic Evaluation of Sanger Validation of Next-Generation Sequencing Variants." Clinical Chemistry 62, no. 4 (April 1, 2016): 647–54. http://dx.doi.org/10.1373/clinchem.2015.249623.
Full textTang, Binhua, Xihan Wang, and 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.
Full textHöing, Ann-Sophie, Alexander E. Volk, and Hanno J. Bolz. "Klinische Anwendung der Hochdurchsatz-Sequenzierung (next-generation sequencing, NGS) bei der Diagnostik des Usher-Syndroms." Optometry & Contact Lenses 3, no. 9 (October 30, 2023): 308–17. http://dx.doi.org/10.54352/dozv.crqo4102.
Full textShetty, Omshree, Mamta Gurav, Prachi Bapat, Nupur Karnik, Gauri Wagh, Trupti Pai, Sridhar Epari, and Sangeeta Desai. "Moving Next-Generation Sequencing into the Clinic." Indian Journal of Medical and Paediatric Oncology 42, no. 03 (May 2021): 221–28. http://dx.doi.org/10.1055/s-0041-1732854.
Full textVodiasova, E. A., E. S. Chelebieva, and O. N. Kuleshova. "The new technologies of high-throughput single-cell RNA sequencing." Vavilov Journal of Genetics and Breeding 23, no. 5 (August 24, 2019): 508–18. http://dx.doi.org/10.18699/vj19.520.
Full textBarry, 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, no. 16_suppl (June 1, 2024): e14031-e14031. http://dx.doi.org/10.1200/jco.2024.42.16_suppl.e14031.
Full textЯнова, Т. И., И. В. Канивец, С. А. Коростелев, Д. В. Пьянков, В. Ю. Удалова, К. В. Горгишели, and Ю. К. Киевская. "NGS for prenatal diagnosis of fetal anomalies." Nauchno-prakticheskii zhurnal «Medicinskaia genetika», no. 11(220) (November 30, 2020): 65–66. http://dx.doi.org/10.25557/2073-7998.2020.11.65-66.
Full textSatam, 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, no. 7 (July 13, 2023): 997. http://dx.doi.org/10.3390/biology12070997.
Full textCohen-Aharonov, Lyora A., Annie Rebibo-Sabbah, Adar Yaacov, Roy Z. Granit, Merav Strauss, Raul Colodner, Ori Cheshin, Shai Rosenberg, and Ronen Eavri. "High throughput SARS-CoV-2 variant analysis using molecular barcodes coupled with next generation sequencing." PLOS ONE 17, no. 6 (June 21, 2022): e0253404. http://dx.doi.org/10.1371/journal.pone.0253404.
Full textChen, Jiajia, Daqing Zhang, Wenying Yan, Dongrong Yang, and 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.
Full textGupta, Piyush Kumar, Rama Shanker Verma, Maria Frolova, and Arkady Ayzenshtadt. "HIGH-THROUGHPUT SEQUENCING ANALYSIS OF MICROBIAL POPULATIONS IN ARCTIC ROCK SAMPLE." SWS Journal of EARTH AND PLANETARY SCIENCES 1, no. 2 (October 1, 2019): 29–38. http://dx.doi.org/10.35603/eps2019/issue2.03.
Full textCorreia, Damien, Olivia Doppelt-Azeroual, Jean-Baptiste Denis, Mathias Vandenbogaert, and Valérie Caro. "MetaGenSense : A web application for analysis and visualization of high throughput sequencing metagenomic data." F1000Research 4 (April 2, 2015): 86. http://dx.doi.org/10.12688/f1000research.6139.1.
Full textCorreia, Damien, Olivia Doppelt-Azeroual, Jean-Baptiste Denis, Mathias Vandenbogaert, and Valérie Caro. "MetaGenSense: A web-application for analysis and exploration of high throughput sequencing metagenomic data." F1000Research 4 (August 22, 2016): 86. http://dx.doi.org/10.12688/f1000research.6139.2.
Full textCorreia, Damien, Olivia Doppelt-Azeroual, Jean-Baptiste Denis, Mathias Vandenbogaert, and Valérie Caro. "MetaGenSense: A web-application for analysis and exploration of high throughput sequencing metagenomic data." F1000Research 4 (December 1, 2016): 86. http://dx.doi.org/10.12688/f1000research.6139.3.
Full textMa, 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, no. 23 (December 3, 2015): 1388. http://dx.doi.org/10.1182/blood.v126.23.1388.1388.
Full textWesołowski, Wojciech, Beata Domnicz, Joanna Augustynowicz, and 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, no. 5 (May 20, 2021): e1008980. http://dx.doi.org/10.1371/journal.pcbi.1008980.
Full textThomson, 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, no. 10 (July 6, 2016): 2470–84. http://dx.doi.org/10.1128/jcm.00330-16.
Full textKhan, Anwar, Nagehan Pakasticali, Omar Fathalla, Taiga Nishihori, and 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 (November 5, 2021): 1625. http://dx.doi.org/10.1182/blood-2021-154418.
Full textHarris, Marian, Donna S. Neuberg, Jianbiao Zheng, Malek Faham, Stephen E. Sallan, and 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, no. 21 (December 6, 2014): 2391. http://dx.doi.org/10.1182/blood.v124.21.2391.2391.
Full textTierno, Domenico, Gabriele Grassi, Serena Scomersi, Marina Bortul, Daniele Generali, Fabrizio Zanconati, and Bruna Scaggiante. "Next-Generation Sequencing and Triple-Negative Breast Cancer: Insights and Applications." International Journal of Molecular Sciences 24, no. 11 (June 2, 2023): 9688. http://dx.doi.org/10.3390/ijms24119688.
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