 High-Throughput Nucleotide Sequencing
"High-Throughput Nucleotide Sequencing" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Techniques of nucleotide sequence analysis that increase the range, complexity, sensitivity, and accuracy of results by greatly increasing the scale of operations and thus the number of nucleotides, and the number of copies of each nucleotide sequenced. The sequencing may be done by analysis of the synthesis or ligation products, hybridization to preexisting sequences, etc.
| Descriptor ID |
D059014
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| MeSH Number(s) |
E05.393.760.319
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| Concept/Terms |
High-Throughput Nucleotide Sequencing- High-Throughput Nucleotide Sequencing
- High Throughput Nucleotide Sequencing
- Nucleotide Sequencing, High-Throughput
- Sequencing, High-Throughput Nucleotide
Massively-Parallel Sequencing- Massively-Parallel Sequencing
- Massively Parallel Sequencing
- Sequencing, Massively-Parallel
- Sequencings, Massively-Parallel
High-Throughput RNA Sequencing- High-Throughput RNA Sequencing
- High Throughput RNA Sequencing
- RNA Sequencing, High-Throughput
- Sequencing, High-Throughput RNA
Deep Sequencing- Deep Sequencing
- Deep Sequencings
- Sequencing, Deep
- Sequencings, Deep
High-Throughput DNA Sequencing- High-Throughput DNA Sequencing
- DNA Sequencing, High-Throughput
- High Throughput DNA Sequencing
- High-Throughput DNA Sequencings
- Sequencing, High-Throughput DNA
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Below are MeSH descriptors whose meaning is more general than "High-Throughput Nucleotide Sequencing".
Below are MeSH descriptors whose meaning is more specific than "High-Throughput Nucleotide Sequencing".
This graph shows the total number of publications written about "High-Throughput Nucleotide Sequencing" by people in this website by year, and whether "High-Throughput Nucleotide Sequencing" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2008 | 0 | 1 | 1 | | 2010 | 1 | 0 | 1 | | 2011 | 3 | 6 | 9 | | 2012 | 6 | 6 | 12 | | 2013 | 10 | 17 | 27 | | 2014 | 11 | 18 | 29 | | 2015 | 7 | 33 | 40 | | 2016 | 8 | 34 | 42 | | 2017 | 9 | 20 | 29 | | 2018 | 21 | 28 | 49 | | 2019 | 11 | 18 | 29 | | 2020 | 2 | 17 | 19 | | 2021 | 6 | 21 | 27 | | 2022 | 5 | 14 | 19 | | 2023 | 1 | 14 | 15 | | 2024 | 6 | 8 | 14 | | 2025 | 4 | 19 | 23 | | 2026 | 1 | 4 | 5 |
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Below are the most recent publications written about "High-Throughput Nucleotide Sequencing" by people in Profiles.
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Yu J, Ahmann LS, Yao YY, Toland A, Snowden A, Ho C, Loyfer N, Kaplan T, Vogel H, Wang L, Howitt BE, Holmes B, Lowe AC, Gu W. Enriched methylomes of low-input and fragmented DNA using fragment ligation EXclusive methylation sequencing. Nucleic Acids Res. 2026 May 05; 54(9).
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Fought MK, Hong G, Quinn AC, Wagner BD, Robertson CE, Harris JK, Laguna TA. Molecular Methods to Detect and Quantify Fungal Communities in Cystic Fibrosis Airway Specimens. Pediatr Pulmonol. 2026 Apr; 61(4):e71598.
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Waliany S, Cooper AJ, Liu SV, Gautschi O, Rotow JK, Smith KER, Weber UM, Lee DH, Loong HHF, Patel JD, Pennell NA, Nagasaka M, Patel SA, Tan DSW, Solomon BJ, Kim TM, Pall G, Riess JW, Sun L, Früh M, Uy NF, Gadgeel S, Feng J, Do A, Falcon C, Leighl NB, Baik CS, Lai GGY, Ou SI, Cheung KSY, Patil T, Mansfield AS, Weiler D, Yeap BY, Wirth LJ, Gainor JF, Drilon A, Lin JJ. Landscape of Genomic Mechanisms of Resistance to Selective RET Inhibitors in RET-Altered Solid Tumors: Analysis of the RETgistry Global Consortium. Clin Cancer Res. 2026 Mar 16; 32(6):1157-1168.
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Schmitz EG, Paul AJ, Ghosh R, Saucier N, Kolicheski A, Risma SI, McDaniels KP, Liu M, Lewis KL, de Jesus AA, Alehashemi S, Fronick CC, Stein D, Dominguez D, Hiraki LT, Lee JH, Norman S, Peng CR, Ward BR, Pettiford LH, Platt A, Lawrence MG, Rocco JM, Al-Herz W, Zerbe CS, Atkinson TP, Peng XP, Allenspach EJ, Hoytema van Konijnenburg DP, Platt CD, Elkins M, Walter JE, Bleesing JJ, Klion A, Ramaswami R, Uzel G, Lionakis MS, Dissanayake D, Su HC, Cortese I, Fuss IJ, Bergerson JRE, Dropulic L, Sereti I, Lisco A, Itan Y, Milner JD, Bogunovic D, Goldbach-Mansky R, Rao VK, Delmonte OM, Notarangelo LD, Keller MD, Durkee-Shock J, Cohen JI, Similuk MN, Holland SM, Griffith M, Griffith OL, Vogel TP, Canna S, Freeman AF, Walkiewicz MA, Cooper MA. Targeted deep sequencing identifies mosaicism in patients with immune dysregulation. J Allergy Clin Immunol. 2026 May; 157(5):1179-1194.
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Chu VT, Spottiswoode N, Ward R, Yokoe DS, Ramirez-Avila L, Phelps MS, Glascock A, Crawford ED, Kamm J, Hao S, Li L, Dynerman D, Waltari E, Nafees S, Kalantar KL, Caldera S, Madera S, Guerrero ES, Ivashin D, Serpa PH, Love C, Mwakibete LL, Doernberg SB, Kistler A, Alvino R, Engel J, Chiu CY, Pak C, Cunningham G, Reyes H, Buie B, Messacar K, Leroue M, Prince BC, Detweiler AM, Stanley K, Caughell C, McNeil N, Neff N, Nichols A, Miller S, DeRisi JL, Tato CM, Langelier CR. Implementation and outcomes of a rapid response genomic hospital epidemiology programme at an academic medical centre over 7 years. Lancet Microbe. 2026 Feb; 7(2):101277.
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Russell JN, Kos D, Yacoub E, Sies AN, Warr B, Jelinski M, Ruzzini A, Cameron ADS. Enhanced metagenomic surveillance for bovine respiratory disease pathogens and antimicrobial resistance by hybridization capture sequencing. Appl Environ Microbiol. 2025 Oct 22; 91(10):e0097725.
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Pitsava G, Hawley M, Auriga L, de Dios I, Ko A, Marmolejos S, Almalvez M, Chen I, Scozzaro K, Zhao J, Barrick R, Ah Mew N, Fusaro VA, LoTempio J, Taylor M, Mestroni L, Graw S, Milewicz D, Guo D, Murdock DR, Bujakowska KM, Xiao C, Délot EC, Berger SI, Vilain E. Genome sequencing reveals the impact of pseudoexons in rare genetic disease. Genet Med. 2025 Nov; 27(11):101574.
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Liu X, Tang YH, Blachly J, Edge S, Jakubek YA, McCarter M, Naqash AR, Nepple KG, Osman A, Reilley MJ, Riedlinger G, Salhia B, Schneider BP, Shriver C, Churchman ML, Rounbehler RJ, Teer JK, Gillis N, Teng M. qcCHIP: an R package to identify clonal hematopoiesis variants using cohort-specific data characteristics. Bioinformatics. 2025 Sep 01; 41(9).
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Rizkalla CN, Tretiakova M, Suarez CJ, Williamson SR, Al-Obaidy KI, Acosta AM, Idrees MT, Chan E, Potterveld S, Sangoi AR. Urothelial carcinoma with osteoclast-like giant cells: An expanded immunohistochemical and molecular profile. Am J Clin Pathol. 2025 08 26; 164(2):257-264.
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Ungar WJ, Wu V, Marshall CR, Hwang J, Hayeems RZ, Tsiplova K, Gillespie MK, Szuto A, Chisholm C, Stavropoulos DJ, Venkataramanan V, Xiao B, Costain G, Bergeron MB, Sawyer S, Lau L, Huang L, Mendoza-Londono R, Somerville MJ, Boycott KM. A microcosting and cost consequence analysis from a randomized controlled trial comparing genome sequencing with exome sequencing for genetic diagnosis. Genet Med. 2026 Feb; 28(2):101561.
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