"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 |
|---|
| 2000 | 0 | 1 | 1 |
| 2010 | 0 | 2 | 2 |
| 2015 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Sequence Analysis, DNA" by people in Profiles.
-
Effect of cytomegalovirus and Epstein-Barr virus replication on intestinal mucosal gene expression and microbiome composition of HIV-infected and uninfected individuals. AIDS. 2017 09 24; 31(15):2059-2067.
-
Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumours. Orphanet J Rare Dis. 2015 Aug 25; 10:103.
-
CD33: increased inclusion of exon 2 implicates the Ig V-set domain in Alzheimer's disease susceptibility. Hum Mol Genet. 2014 May 15; 23(10):2729-36.
-
Phenotypic properties of transmitted founder HIV-1. Proc Natl Acad Sci U S A. 2013 Apr 23; 110(17):6626-33.
-
Comparison of PHOX2B testing methods in the diagnosis of congenital central hypoventilation syndrome and mosaic carriers. Diagn Mol Pathol. 2010 Dec; 19(4):224-31.
-
Array-based FMR1 sequencing and deletion analysis in patients with a fragile X syndrome-like phenotype. PLoS One. 2010 Mar 05; 5(3):e9476.
-
Molecular and enzymatic characterization of Schistosoma mansoni thioredoxin peroxidase. J Parasitol. 2000 Oct; 86(5):908-15.
-
Absence of cell-surface annexin V is accompanied by defective collagen matrix binding in the Swarm rat chondrosarcoma. J Cell Biochem. 1997 May; 65(2):131-44.