 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.
A multistage process that includes cloning, physical mapping, subcloning, determination of the DNA SEQUENCE, and information analysis.
| Descriptor ID |
D017422
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| MeSH Number(s) |
E05.393.760.700
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| 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
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Below are MeSH descriptors whose meaning is more general than "Sequence Analysis, DNA".
Below are MeSH descriptors whose meaning is more specific than "Sequence Analysis, DNA".
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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1992 | 1 | 0 | 1 | | 1993 | 0 | 8 | 8 | | 1994 | 1 | 4 | 5 | | 1995 | 1 | 8 | 9 | | 1996 | 1 | 5 | 6 | | 1997 | 0 | 15 | 15 | | 1998 | 1 | 6 | 7 | | 1999 | 0 | 7 | 7 | | 2000 | 1 | 11 | 12 | | 2001 | 2 | 10 | 12 | | 2002 | 1 | 25 | 26 | | 2003 | 3 | 17 | 20 | | 2004 | 3 | 27 | 30 | | 2005 | 1 | 23 | 24 | | 2006 | 5 | 16 | 21 | | 2007 | 2 | 25 | 27 | | 2008 | 2 | 26 | 28 | | 2009 | 4 | 26 | 30 | | 2010 | 5 | 23 | 28 | | 2011 | 10 | 36 | 46 | | 2012 | 10 | 51 | 61 | | 2013 | 13 | 31 | 44 | | 2014 | 9 | 37 | 46 | | 2015 | 8 | 42 | 50 | | 2016 | 6 | 25 | 31 | | 2017 | 5 | 33 | 38 | | 2018 | 3 | 15 | 18 | | 2019 | 6 | 13 | 19 | | 2020 | 1 | 3 | 4 |
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Below are the most recent publications written about "Sequence Analysis, DNA" by people in Profiles.
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Nelsen MP, Lücking R, Boyce CK, Lumbsch HT, Ree RH. The macroevolutionary dynamics of symbiotic and phenotypic diversification in lichens. Proc Natl Acad Sci U S A. 2020 09 01; 117(35):21495-21503.
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Wu T, Lyu R, You Q, He C. Kethoxal-assisted single-stranded DNA sequencing captures global transcription dynamics and enhancer activity in situ. Nat Methods. 2020 05; 17(5):515-523.
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Sedlock JL, Heaney LR, Balete DS, Ruedi M. Philippine bats of the genus Kerivoula (Chiroptera: Vespertilionidae): Overview and assessment of variation in K. pellucida and K. whiteheadi. Zootaxa. 2020 Mar 25; 4755(3):zootaxa.4755.3.2.
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Marcus JH, Posth C, Ringbauer H, Lai L, Skeates R, Sidore C, Beckett J, Furtwängler A, Olivieri A, Chiang CWK, Al-Asadi H, Dey K, Joseph TA, Liu CC, Der Sarkissian C, Radzeviciute R, Michel M, Gradoli MG, Marongiu P, Rubino S, Mazzarello V, Rovina D, La Fragola A, Serra RM, Bandiera P, Bianucci R, Pompianu E, Murgia C, Guirguis M, Orquin RP, Tuross N, van Dommelen P, Haak W, Reich D, Schlessinger D, Cucca F, Krause J, Novembre J. Genetic history from the Middle Neolithic to present on the Mediterranean island of Sardinia. Nat Commun. 2020 02 24; 11(1):939.
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Ganna A, Verweij KJH, Nivard MG, Maier R, Wedow R, Busch AS, Abdellaoui A, Guo S, Sathirapongsasuti JF. Genome studies must account for history-Response. Science. 2019 12 20; 366(6472):1461-1462.
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Ritterhouse LL, Parilla M, Zhen CJ, Wurst MN, Puranik R, Henderson CM, Joudeh NZ, Hartley MJ, Haridas R, Wanjari P, Furtado LV, Kadri S, Segal JP. Clinical Validation and Implementation of a Measurable Residual Disease Assay for NPM1 in Acute Myeloid Leukemia by Error-Corrected Next-Generation Sequencing. Mol Diagn Ther. 2019 12; 23(6):791-802.
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Barr K, Reinitz J, Radulescu O. An in silico analysis of robust but fragile gene regulation links enhancer length to robustness. PLoS Comput Biol. 2019 11; 15(11):e1007497.
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Grzybowski AT, Shah RN, Richter WF, Ruthenburg AJ. Native internally calibrated chromatin immunoprecipitation for quantitative studies of histone post-translational modifications. Nat Protoc. 2019 12; 14(12):3275-3302.
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Ross LF, Clayton EW. Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq. Pediatrics. 2019 12; 144(6).
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Balagopal V, Hantel A, Kadri S, Steinhardt G, Zhen CJ, Kang W, Wanjari P, Ritterhouse LL, Stock W, Segal JP. Measurable residual disease monitoring for patients with acute myeloid leukemia following hematopoietic cell transplantation using error corrected hybrid capture next generation sequencing. PLoS One. 2019; 14(10):e0224097.
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