Oligonucleotide Array Sequence Analysis
"Oligonucleotide Array Sequence Analysis" 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.
Hybridization of a nucleic acid sample to a very large set of OLIGONUCLEOTIDE PROBES, which have been attached individually in columns and rows to a solid support, to determine a BASE SEQUENCE, or to detect variations in a gene sequence, GENE EXPRESSION, or for GENE MAPPING.
| Descriptor ID |
D020411
|
| MeSH Number(s) |
E05.393.661.640 E05.393.760.640 E05.588.570.660 E05.601.640
|
| Concept/Terms |
cDNA Microarrays- cDNA Microarrays
- Microarray, cDNA
- Microarrays, cDNA
- cDNA Microarray
- cDNA Arrays
- Array, cDNA
- Arrays, cDNA
- cDNA Array
Gene Chips- Gene Chips
- Chip, Gene
- Chips, Gene
- Gene Chip
Oligonucleotide Arrays- Oligonucleotide Arrays
- Array, Oligonucleotide
- Arrays, Oligonucleotide
- Oligonucleotide Array
- Oligonucleotide Microarrays
- Microarray, Oligonucleotide
- Microarrays, Oligonucleotide
- Oligonucleotide Microarray
DNA Microarrays- DNA Microarrays
- DNA Microarray
- Microarray, DNA
- Microarrays, DNA
- DNA Chips
- Chip, DNA
- Chips, DNA
- DNA Chip
- DNA Microchips
- DNA Microchip
- Microchip, DNA
- Microchips, DNA
- DNA Arrays
- Array, DNA
- Arrays, DNA
- DNA Array
|
Below are MeSH descriptors whose meaning is more general than "Oligonucleotide Array Sequence Analysis".
Below are MeSH descriptors whose meaning is more specific than "Oligonucleotide Array Sequence Analysis".
This graph shows the total number of publications written about "Oligonucleotide Array Sequence Analysis" by people in this website by year, and whether "Oligonucleotide Array Sequence Analysis" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1999 | 0 | 2 | 2 |
| 2000 | 2 | 0 | 2 |
| 2001 | 4 | 6 | 10 |
| 2002 | 13 | 20 | 33 |
| 2003 | 9 | 28 | 37 |
| 2004 | 11 | 42 | 53 |
| 2005 | 9 | 34 | 43 |
| 2006 | 15 | 32 | 47 |
| 2007 | 5 | 27 | 32 |
| 2008 | 6 | 51 | 57 |
| 2009 | 3 | 39 | 42 |
| 2010 | 4 | 37 | 41 |
| 2011 | 2 | 30 | 32 |
| 2012 | 3 | 20 | 23 |
| 2013 | 1 | 15 | 16 |
| 2014 | 1 | 12 | 13 |
| 2015 | 3 | 13 | 16 |
| 2016 | 2 | 4 | 6 |
| 2017 | 1 | 3 | 4 |
| 2018 | 0 | 6 | 6 |
| 2020 | 0 | 1 | 1 |
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Below are the most recent publications written about "Oligonucleotide Array Sequence Analysis" by people in Profiles.
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Sporadic oncocytic tumors with features intermediate between oncocytoma and chromophobe renal cell carcinoma: comprehensive clinicopathological and genomic profiling. Hum Pathol. 2020 10; 104:18-29.
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Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol?Use. Biol Psychiatry. 2019 06 01; 85(11):946-955.
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The NCI Transcriptional Pharmacodynamics Workbench: A Tool to Examine Dynamic Expression Profiling of Therapeutic Response in the NCI-60 Cell Line Panel. Cancer Res. 2018 12 15; 78(24):6807-6817.
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A Predictive 7-Gene Assay and Prognostic Protein Biomarkers for Non-small Cell Lung Cancer. EBioMedicine. 2018 Jun; 32:102-110.
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Surgical necrotizing enterocolitis in extremely premature neonates is associated with genetic variations in an intergenic region of chromosome 8. Pediatr Res. 2018 05; 83(5):943-953.
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Exosomal Cargo Properties, Endothelial Function and Treatment of Obesity Hypoventilation Syndrome: A Proof of Concept Study. J Clin Sleep Med. 2018 05 15; 14(5):797-807.
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Global DNA methylation changes spanning puberty are near predicted estrogen-responsive genes and enriched for genes involved in endocrine and immune processes. Clin Epigenetics. 2018; 10:62.
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Genome-Wide DNA Methylation Profiles of Phlegm-Dampness Constitution. Cell Physiol Biochem. 2018; 45(5):1999-2008.
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Long ncRNA Landscape in the Ileum of Treatment-Naive Early-Onset Crohn Disease. Inflamm Bowel Dis. 2018 01 18; 24(2):346-360.
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Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3. Circ Cardiovasc Genet. 2017 Oct; 10(5).