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
|
| MeSH Number(s) |
E05.393.760.319
|
| 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
|
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.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 1 | 1 | 2 |
| 2011 | 3 | 6 | 9 |
| 2012 | 11 | 12 | 23 |
| 2013 | 11 | 14 | 25 |
| 2014 | 15 | 25 | 40 |
| 2015 | 14 | 44 | 58 |
| 2016 | 25 | 54 | 79 |
| 2017 | 18 | 27 | 45 |
| 2018 | 13 | 46 | 59 |
| 2019 | 10 | 20 | 30 |
| 2020 | 9 | 35 | 44 |
| 2021 | 15 | 26 | 41 |
| 2022 | 6 | 18 | 24 |
| 2023 | 2 | 15 | 17 |
| 2024 | 8 | 20 | 28 |
| 2025 | 6 | 14 | 20 |
| 2026 | 1 | 5 | 6 |
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Below are the most recent publications written about "High-Throughput Nucleotide Sequencing" by people in Profiles.
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Assessing the readiness of Oxford Nanopore sequencing for clinical genomics applications. Genome Res. 2026 03 02; 36(3):460-471.
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STRspy2.0: Unlocking the Potential of Long Reads for Forensic DNA Profiling. Int J Mol Sci. 2026 Feb 16; 27(4).
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Targeted deep sequencing identifies mosaicism in patients with immune dysregulation. J Allergy Clin Immunol. 2026 May; 157(5):1179-1194.
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Comprehensive profiling of the human tear fluid miRNome using small RNA sequencing. Ocul Surf. 2026 Apr; 40:133-143.
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Whole-Genome Amplification on Single Circulating Trophoblast Cell. Methods Mol Biol. 2026; 3003:11-23.
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Microbiome Profiling in Chagas Disease: Sample Collection, Sequencing, and Analysis. Methods Mol Biol. 2026; 3013:265-297.
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From PKU to Genome Sequencing: The Past, Present, and Future of Newborn Screening. Clin Chem. 2025 Dec 30; 72(1):123-132.
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Clair3-RNA: a deep learning-based small variant caller for long-read RNA sequencing data. Nat Commun. 2025 Dec 22; 16(1):11553.
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CountASAP: a lightweight, easy to use python package for processing ASAPseq data. BMC Bioinformatics. 2025 Nov 27; 26(1):307.
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Application of FreezeTB, a targeted nanopore sequencing assay, for identification of drug resistance and lineages among pulmonary tuberculosis cases in Alaska. Microbiol Spectr. 2026 Jan 06; 14(1):e0233525.