"DNA, Intergenic" 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.
Any of the DNA in between gene-coding DNA, including untranslated regions, 5' and 3' flanking regions, INTRONS, non-functional pseudogenes, and non-functional repetitive sequences. This DNA may or may not encode regulatory functions.
Descriptor ID |
D021901
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MeSH Number(s) |
D13.444.308.324 G05.360.340.024.220
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Concept/Terms |
DNA, Intergenic- DNA, Intergenic
- DNAs, Intergenic
- Intergenic DNAs
- Intergenic DNA
Spacer DNA- Spacer DNA
- DNAs, Spacer
- Spacer DNAs
- DNA, Spacer
Intergenic Sequence- Intergenic Sequence
- Intergenic Sequences
- Sequences, Intergenic
- Intercistronic Sequence
- Intercistronic Sequences
- Sequence, Intercistronic
- Sequences, Intercistronic
- Sequence, Intergenic
DNA, Junk- DNA, Junk
- DNAs, Junk
- Junk DNAs
- Junk DNA
Intergenic Region- Intergenic Region
- Intergenic Regions
- Region, Intergenic
- Regions, Intergenic
- Intercistronic Region
- Intercistronic Regions
- Region, Intercistronic
- Regions, Intercistronic
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Below are MeSH descriptors whose meaning is more general than "DNA, Intergenic".
Below are MeSH descriptors whose meaning is more specific than "DNA, Intergenic".
This graph shows the total number of publications written about "DNA, Intergenic" by people in this website by year, and whether "DNA, Intergenic" was a major or minor topic of these publications.
To see the data from this visualization as text,
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Year | Major Topic | Minor Topic | Total |
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2001 | 0 | 1 | 1 |
2003 | 1 | 1 | 2 |
2004 | 0 | 1 | 1 |
2005 | 0 | 2 | 2 |
2008 | 0 | 1 | 1 |
2010 | 1 | 1 | 2 |
2013 | 0 | 1 | 1 |
2014 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2017 | 2 | 2 | 4 |
2021 | 0 | 1 | 1 |
2022 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "DNA, Intergenic" by people in Profiles.
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Functional correlation of genome-wide DNA methylation profiles in genetic neurodevelopmental disorders. Hum Mutat. 2022 11; 43(11):1609-1628.
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Prioritizing non-coding regions based on human genomic constraint and sequence context with deep learning. Nat Commun. 2021 03 08; 12(1):1504.
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Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples. Nat Commun. 2020 09 21; 11(1):4748.
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Nuclease integrated kinase super assemblies (NiKs) and their role in RNA processing. Curr Genet. 2018 Feb; 64(1):183-190.
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Identification of a novel locus associated with skin colour in African-admixed populations. Sci Rep. 2017 03 16; 7:44548.
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Genomic approaches to the assessment of human spina bifida risk. Birth Defects Res. 2017 01 30; 109(2):120-128.
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Molecular identification and genotyping of Trypanosoma cruzi DNA in autochthonous Chagas disease patients from Texas, USA. Infect Genet Evol. 2017 04; 49:151-156.
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TriXY-Homogeneous genetic sexing of highly degraded forensic samples including hair shafts. Forensic Sci Int Genet. 2016 11; 25:166-174.
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Population genomic analysis of 962 whole genome sequences of humans reveals natural selection in non-coding regions. PLoS One. 2015; 10(3):e0121644.
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Quantitative modeling of a gene's expression from its intergenic sequence. PLoS Comput Biol. 2014 Mar; 10(3):e1003467.