"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
|
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".
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 |
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1995 | 0 | 1 | 1 |
1996 | 0 | 2 | 2 |
1997 | 0 | 3 | 3 |
1998 | 0 | 1 | 1 |
1999 | 0 | 1 | 1 |
2000 | 0 | 2 | 2 |
2001 | 1 | 0 | 1 |
2002 | 1 | 0 | 1 |
2003 | 4 | 6 | 10 |
2004 | 3 | 1 | 4 |
2005 | 0 | 4 | 4 |
2006 | 3 | 3 | 6 |
2007 | 1 | 4 | 5 |
2008 | 5 | 4 | 9 |
2009 | 2 | 3 | 5 |
2010 | 1 | 7 | 8 |
2011 | 5 | 7 | 12 |
2012 | 1 | 21 | 22 |
2013 | 4 | 10 | 14 |
2014 | 7 | 19 | 26 |
2015 | 5 | 15 | 20 |
2016 | 5 | 14 | 19 |
2017 | 2 | 9 | 11 |
2018 | 1 | 7 | 8 |
2019 | 3 | 5 | 8 |
2020 | 2 | 6 | 8 |
2021 | 1 | 7 | 8 |
2022 | 1 | 2 | 3 |
2023 | 0 | 2 | 2 |
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Below are the most recent publications written about "Sequence Analysis, DNA" by people in Profiles.
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Reliable genotyping of recombinant genomes using a robust hidden Markov model. Plant Physiol. 2023 05 31; 192(2):821-836.
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Benchmarking of structural variant detection in the tetraploid potato genome using linked-read sequencing. Genomics. 2023 03; 115(2):110568.
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Identification of genome edited cells using CRISPRnano. Nucleic Acids Res. 2022 07 05; 50(W1):W199-W203.
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A chromosome scale tomato genome built from complementary PacBio and Nanopore sequences alone reveals extensive linkage drag during breeding. Plant J. 2022 04; 110(2):572-588.
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Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT4 in the formation of primary congenital chylothorax. Am J Med Genet A. 2022 05; 188(5):1607-1611.
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Accurate and scalable variant calling from single cell DNA sequencing data with ProSolo. Nat Commun. 2021 11 18; 12(1):6744.
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Aiming off the target: recycling target capture sequencing reads for investigating repetitive DNA. Ann Bot. 2021 11 09; 128(7):835-848.
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Chromatin-accessibility estimation from single-cell ATAC-seq data with scOpen. Nat Commun. 2021 11 04; 12(1):6386.
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Detection of mobile elements insertions for routine clinical diagnostics in targeted sequencing data. Mol Genet Genomic Med. 2021 12; 9(12):e1807.
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Rodentibacter haemolyticus sp. nov. isolated from laboratory rodents. Int J Syst Evol Microbiol. 2021 Aug; 71(8).