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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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".

Analytical, Diagnostic and Therapeutic Techniques and Equipment [E]
Investigative Techniques [E05]
Genetic Techniques [E05.393]
Sequence Analysis [E05.393.760]
High-Throughput Nucleotide Sequencing [E05.393.760.319]

Below are MeSH descriptors whose meaning is related to "High-Throughput Nucleotide Sequencing".

Below are MeSH descriptors whose meaning is more specific than "High-Throughput Nucleotide Sequencing".

publications

Timeline | Most Recent

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.

Bar chart showing 92 publications over 10 distinct years, with a maximum of 20 publications in 2015

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2011	0	2	2
2013	0	3	3
2014	4	9	13
2015	4	16	20
2016	1	9	10
2017	1	6	7
2018	6	7	13
2019	5	9	14
2020	2	7	9
2021	0	1	1

Below are the most recent publications written about "High-Throughput Nucleotide Sequencing" by people in Profiles.

Allen RA, Williams CL, Penrod Y, McCloskey C, Carpenter-Azevedo K, Huard RC, King E, Terence Dunn S. A pyrosequencing protocol for rapid identification of SARS-CoV-2 variants. J Med Virol. 2022 Aug; 94(8):3661-3668.

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Zhou Z, Li M. Targeted therapies for cancer. BMC Med. 2022 03 11; 20(1):90.

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Lane BM, Chryst-Stangl M, Wu G, Shalaby M, El Desoky S, Middleton CC, Huggins K, Sood A, Ochoa A, Malone AF, Vancini R, Miller SE, Hall G, Kim SY, Howell DN, Kari JA, Gbadegesin R. Steroid-sensitive nephrotic syndrome candidate gene CLVS1 regulates podocyte oxidative stress and endocytosis. JCI Insight. 2022 01 25; 7(2).

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Sanchez-Contreras M, Sweetwyne MT, Kohrn BF, Tsantilas KA, Hipp MJ, Schmidt EK, Fredrickson J, Whitson JA, Campbell MD, Rabinovitch PS, Marcinek DJ, Kennedy SR. A replication-linked mutational gradient drives somatic mutation accumulation and influences germline polymorphisms and genome composition in mitochondrial DNA. Nucleic Acids Res. 2021 11 08; 49(19):11103-11118.

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Farcas M, Gatalica Z, Trpkov K, Swensen J, Zhou M, Alaghehbandan R, Williamson SR, Magi-Galluzzi C, Gill AJ, Tretiakova M, Lopez JI, Montiel DP, Sperga M, Comperat E, Brimo F, Yilmaz A, Siadat F, Sangoi A, Gao Y, Ptákova N, Kuthi L, Pivovarcikova K, Rogala J, Agaimy A, Hartmann A, Fraune C, Rychly B, Hurnik P, Durcansky D, Bonert M, Gakis G, Michal M, Hora M, Hes O. Eosinophilic vacuolated tumor (EVT) of kidney demonstrates sporadic TSC/MTOR mutations: next-generation sequencing multi-institutional study of 19 cases. Mod Pathol. 2022 03; 35(3):344-351.

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Judd J, Abdel Karim N, Khan H, Naqash AR, Baca Y, Xiu J, VanderWalde AM, Mamdani H, Raez LE, Nagasaka M, Pai SG, Socinski MA, Nieva JJ, Kim C, Wozniak AJ, Ikpeazu C, de Lima Lopes G, Spira AI, Korn WM, Kim ES, Liu SV, Borghaei H. Characterization of KRAS Mutation Subtypes in Non-small Cell Lung Cancer. Mol Cancer Ther. 2021 12; 20(12):2577-2584.

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Colli LM, Jessop L, Myers TA, Camp SY, Machiela MJ, Choi J, Cunha R, Onabajo O, Mills GC, Schmid V, Brodie SA, Delattre O, Mole DR, Purdue MP, Yu K, Brown KM, Chanock SJ. Altered regulation of DPF3, a member of the SWI/SNF complexes, underlies the 14q24 renal cancer susceptibility locus. Am J Hum Genet. 2021 09 02; 108(9):1590-1610.

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Prieto-Granada C, Morlote D, Pavlidakey P, Rodriguez-Waitkus P, Ramirez C, Florento E, Swensen J, Gatalica Z, Stevens TM. Poroid adnexal skin tumors with YAP1 fusions exhibit similar histopathologic features: A series of six YAP1-rearranged adnexal skin tumors. J Cutan Pathol. 2021 Sep; 48(9):1139-1149.

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Rodin RE, Dou Y, Kwon M, Sherman MA, D'Gama AM, Doan RN, Rento LM, Girskis KM, Bohrson CL, Kim SN, Nadig A, Luquette LJ, Gulhan DC, Park PJ, Walsh CA. The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing. Nat Neurosci. 2021 02; 24(2):176-185.

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Raj P, Song R, Zhu H, Riediger L, Jun DJ, Liang C, Arana C, Zhang B, Gao Y, Wakeland BE, Dozmorov I, Zhou J, Kelly JA, Lauwerys BR, Guthridge JM, Olsen NJ, Nath SK, Pasare C, van Oers N, Gilkeson G, Tsao BP, Gaffney PM, Gregersen PK, James JA, Zuo X, Karp DR, Li QZ, Wakeland EK. Deep sequencing reveals a DAP1 regulatory haplotype that potentiates autoimmunity in systemic lupus erythematosus. Genome Biol. 2020 11 19; 21(1):281.

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