 Databases, Nucleic Acid
"Databases, Nucleic Acid" 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.
Databases containing information about NUCLEIC ACIDS such as BASE SEQUENCE; SNPS; NUCLEIC ACID CONFORMATION; and other properties. Information about the DNA fragments kept in a GENE LIBRARY or GENOMIC LIBRARY is often maintained in DNA databases.
| Descriptor ID |
D030561
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| MeSH Number(s) |
L01.313.500.750.300.188.400.300.500 L01.313.500.750.300.188.400.325.630 L01.470.750.750.300.500 L01.470.750.750.325.630
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| Concept/Terms |
DNA Databases- DNA Databases
- DNA Database
- Database, DNA
- DNA Data Banks
- Bank, DNA Data
- Banks, DNA Data
- DNA Data Bank
- Data Bank, DNA
- Data Banks, DNA
- DNA Databanks
- DNA Databank
- Databank, DNA
- Databanks, DNA
- Databases, DNA
DNA Sequence Databases- DNA Sequence Databases
- DNA Sequence Database
- Database, DNA Sequence
- Sequence Database, DNA
- Sequence Databases, DNA
- Databases, DNA Sequence
RNA Sequence Databases- RNA Sequence Databases
- Database, RNA Sequence
- RNA Sequence Database
- Sequence Database, RNA
- Sequence Databases, RNA
- Databases, RNA Sequence
RNA Databases- RNA Databases
- Database, RNA
- RNA Database
- Databases, RNA
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Below are MeSH descriptors whose meaning is more general than "Databases, Nucleic Acid".
- Information Science [L]
- Information Science [L01]
- Informatics [L01.313]
- Medical Informatics [L01.313.500]
- Medical Informatics Applications [L01.313.500.750]
- Information Systems [L01.313.500.750.300]
- Databases as Topic [L01.313.500.750.300.188]
- Databases, Factual [L01.313.500.750.300.188.400]
- Databases, Chemical [L01.313.500.750.300.188.400.300]
- Databases, Nucleic Acid [L01.313.500.750.300.188.400.300.500]
- Databases, Genetic [L01.313.500.750.300.188.400.325]
- Databases, Nucleic Acid [L01.313.500.750.300.188.400.325.630]
- Information Storage and Retrieval [L01.470]
- Databases as Topic [L01.470.750]
- Databases, Factual [L01.470.750.750]
- Databases, Chemical [L01.470.750.750.300]
- Databases, Nucleic Acid [L01.470.750.750.300.500]
- Databases, Genetic [L01.470.750.750.325]
- Databases, Nucleic Acid [L01.470.750.750.325.630]
Below are MeSH descriptors whose meaning is more specific than "Databases, Nucleic Acid".
This graph shows the total number of publications written about "Databases, Nucleic Acid" by people in this website by year, and whether "Databases, Nucleic Acid" 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 |
|---|
| 2001 | 2 | 0 | 2 | | 2004 | 0 | 2 | 2 | | 2005 | 1 | 0 | 1 | | 2006 | 1 | 0 | 1 | | 2008 | 0 | 1 | 1 | | 2009 | 0 | 3 | 3 | | 2013 | 1 | 0 | 1 | | 2014 | 0 | 2 | 2 | | 2015 | 0 | 1 | 1 | | 2016 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 | | 2020 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Databases, Nucleic Acid" by people in Profiles.
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Yao RA, Akinrinade O, Chaix M, Mital S. Quality of whole genome sequencing from blood versus saliva derived DNA in cardiac patients. BMC Med Genomics. 2020 01 29; 13(1):11.
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Lee TH, Kim J, Robertson JS, Paterson AH. Plant Genome Duplication Database. Methods Mol Biol. 2017; 1533:267-277.
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Dyke SO, Philippakis AA, Rambla De Argila J, Paltoo DN, Luetkemeier ES, Knoppers BM, Brookes AJ, Spalding JD, Thompson M, Roos M, Boycott KM, Brudno M, Hurles M, Rehm HL, Matern A, Fiume M, Sherry ST. Consent Codes: Upholding Standard Data Use Conditions. PLoS Genet. 2016 Jan; 12(1):e1005772.
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Thapar A, Martin J, Mick E, Arias Vásquez A, Langley K, Scherer SW, Schachar R, Crosbie J, Williams N, Franke B, Elia J, Glessner J, Hakonarson H, Owen MJ, Faraone SV, O'Donovan MC, Holmans P. Psychiatric gene discoveries shape evidence on ADHD's biology. Mol Psychiatry. 2016 09; 21(9):1202-7.
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Woodbury-Smith M, Paterson AD, Thiruvahindrapduram B, Lionel AC, Marshall CR, Merico D, Fernandez BA, Duku E, Sutcliffe JS, O'Conner I, Chrysler C, Thompson A, Kellam B, Tammimies K, Walker S, Yuen RK, Uddin M, Howe JL, Parlier M, Whitten K, Szatmari P, Vieland VJ, Piven J, Scherer SW. Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes. Hum Genet. 2015 Feb; 134(2):191-201.
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Savoia A, Kunishima S, De Rocco D, Zieger B, Rand ML, Pujol-Moix N, Caliskan U, Tokgoz H, Pecci A, Noris P, Srivastava A, Ward C, Morel-Kopp MC, Alessi MC, Bellucci S, Beurrier P, de Maistre E, Favier R, Hézard N, Hurtaud-Roux MF, Latger-Cannard V, Lavenu-Bombled C, Proulle V, Meunier S, Négrier C, Nurden A, Randrianaivo H, Fabris F, Platokouki H, Rosenberg N, HadjKacem B, Heller PG, Karimi M, Balduini CL, Pastore A, Lanza F. Spectrum of the mutations in Bernard-Soulier syndrome. Hum Mutat. 2014 Sep; 35(9):1033-45.
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MacDonald JR, Ziman R, Yuen RK, Feuk L, Scherer SW. The Database of Genomic Variants: a curated collection of structural variation in the human genome. Nucleic Acids Res. 2014 Jan; 42(Database issue):D986-92.
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Lee S, Hormozdiari F, Alkan C, Brudno M. MoDIL: detecting small indels from clone-end sequencing with mixtures of distributions. Nat Methods. 2009 Jul; 6(7):473-4.
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Boles MK, Wilkinson BM, Maxwell A, Lai L, Mills AA, Nishijima I, Salinger AP, Moskowitz I, Hirschi KK, Liu B, Bradley A, Justice MJ. A mouse chromosome 4 balancer ENU-mutagenesis screen isolates eleven lethal lines. BMC Genet. 2009 Mar 06; 10:12.
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Dubchak I, Poliakov A, Kislyuk A, Brudno M. Multiple whole-genome alignments without a reference organism. Genome Res. 2009 Apr; 19(4):682-9.
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