Sequence Analysis, DNA

"Sequence Analysis, DNA" 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

A multistage process that includes cloning, physical mapping, subcloning, determination of the DNA SEQUENCE, and information analysis.

Descriptor ID	D017422
MeSH Number(s)	E05.393.760.700
Concept/Terms	Sequence Analysis, DNA Sequence Analysis, DNA Analyses, DNA Sequence DNA Sequence Analyses Sequence Analyses, DNA Analysis, DNA Sequence DNA Sequence Analysis Sequence Determinations, DNA Sequence Determinations, DNA Determinations, DNA Sequence Sequence Determination, DNA DNA Sequence Determinations DNA Sequencing Sequencing, DNA Determination, DNA Sequence DNA Sequence Determination

Below are MeSH descriptors whose meaning is more general than "Sequence Analysis, DNA".

Analytical, Diagnostic and Therapeutic Techniques and Equipment [E]
Investigative Techniques [E05]
Genetic Techniques [E05.393]
Sequence Analysis [E05.393.760]
Sequence Analysis, DNA [E05.393.760.700]

Below are MeSH descriptors whose meaning is related to "Sequence Analysis, DNA".

Below are MeSH descriptors whose meaning is more specific than "Sequence Analysis, DNA".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Sequence Analysis, DNA" by people in this website by year, and whether "Sequence Analysis, DNA" was a major or minor topic of these publications.

Bar chart showing 344 publications over 31 distinct years, with a maximum of 27 publications in 2014

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

Year	Major Topic	Minor Topic	Total
1996	1	6	7
1997	0	4	4
1998	0	8	8
1999	0	4	4
2000	0	6	6
2001	1	5	6
2002	0	9	9
2003	2	12	14
2004	3	10	13
2005	2	15	17
2006	3	11	14
2007	2	14	16
2008	2	13	15
2009	3	15	18
2010	3	3	6
2011	5	20	25
2012	4	16	20
2013	3	20	23
2014	3	24	27
2015	3	21	24
2016	2	13	15
2017	5	9	14
2018	3	7	10
2019	2	7	9
2020	1	3	4
2021	2	3	5
2022	1	1	2
2023	0	1	1
2024	0	3	3
2025	1	3	4
2026	0	1	1

Below are the most recent publications written about "Sequence Analysis, DNA" by people in Profiles.

Manakhov AD, Rozhdestvenskikh EV, Aituganova ED, Voroshilov AN, Svirkina NG, Kunizheva SS, Andreeva TV, Ostapenko SN, Kuznetsov VD, Rogaev EI. Comparison of Illumina NovaSeq 6000, GeneMind SURFSeq 5000, Salus Evo, and MGI DNBSEQ-G400 for Ancient DNA Whole-Genome Sequencing. Genes (Basel). 2026 07 24; 17(8).

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Liu H, Flavahan W, Zhu LJ. Training Recurrent Neural Networks for BrdU Detection with Oxford Nanopore Sequencing: Guidance and Lessons Learned. Genes (Basel). 2025 Nov 10; 16(11).

View in: PubMed
David SS, Pacheco BA, Kishimoto K, Vantine S, Hu K, Liu H, Davis DL, Tran H, Sallis BF, Ali L, Haynes CM, McCormick BA, Zhu LJ, Flavahan WA. Multidimensional third-generation sequencing of modified DNA bases allows interrogation of complex biological systems. Nat Commun. 2025 Jul 01; 16(1):5676.

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Jinich A, Zaveri A, DeJesus MA, Spencer A, Almada-Monter R, Flores-Bautista E, Smith CM, Sassetti CM, Rock JM, Ehrt S, Schnappinger D, Ioerger TR, Rhee KY. The Mycobacterium tuberculosis Transposon Sequencing Database (MtbTnDB): A Large-Scale Guide to Genetic Conditional Essentiality. Mol Microbiol. 2025 07; 124(1):91-101.

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Tierney AJ, Prajapati SK, Leonetti A, Fola AA, Kwapong SS, Baillargeon KR, Roberds A, Stewart VA, Amoah LE, Bailey JA, Williamson KC, Mace CR. Leukocyte Depletion in Dried Blood Spot Cards Enables Enrichment of Parasite DNA for Improved Sequencing. Anal Chem. 2025 05 13; 97(18):9691-9700.

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Pearman WS, Arranz V, Carvajal JI, Whibley A, Liau Y, Johnson K, Gray R, Treece JM, Gemmell NJ, Liggins L, Fraser CI, Jensen EL, Green NJ. A cry for kelp: Evidence for polyphenolic inhibition of Oxford Nanopore sequencing of brown algae. J Phycol. 2024 12; 60(6):1601-1610.

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Axelsson J, LeBlanc D, Shojaeisaadi H, Meier MJ, Fitzgerald DM, Nachmanson D, Carlson J, Golubeva A, Higgins J, Smith T, Lo FY, Pilsner R, Williams A, Salk J, Marchetti F, Yauk C. Frequency and spectrum of mutations in human sperm measured using duplex sequencing correlate with trio-based de novo mutation analyses. Sci Rep. 2024 10 08; 14(1):23134.

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Abdennur N, Fudenberg G, Flyamer IM, Galitsyna AA, Goloborodko A, Imakaev M, Venev SV. Pairtools: From sequencing data to chromosome contacts. PLoS Comput Biol. 2024 May; 20(5):e1012164.

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Weiss ZF, Pyden AD, Jhaveri TA, Kanjilal S. The diagnostic and clinical utility of microbial cell-free DNA sequencing in a real-world setting. Diagn Microbiol Infect Dis. 2023 Oct; 107(2):116004.

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Lin JN, Lai CH, Lin SY, Lee CC, Lee NY, Liu PY, Yang CH, Huang YH. Effect of Intragenomic Sequence Heterogeneity among Multiple 16S rRNA Genes on Species Identification of Elizabethkingia. Microbiol Spectr. 2022 Oct 26; 10(5):e0133822.

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