"Genotyping Techniques" 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.
Methods used to determine individuals' specific ALLELES or SNPS (single nucleotide polymorphisms).
Descriptor ID |
D060005
|
MeSH Number(s) |
E05.393.442
|
Concept/Terms |
Genotyping Techniques- Genotyping Techniques
- Genotyping Technique
- Technique, Genotyping
- Techniques, Genotyping
- Genotype Assignment Methodology
- Assignment Methodologies, Genotype
- Assignment Methodology, Genotype
- Genotype Assignment Methodologies
- Methodologies, Genotype Assignment
- Methodology, Genotype Assignment
- Genotype Calling Methods
- Calling Method, Genotype
- Calling Methods, Genotype
- Genotype Calling Method
- Method, Genotype Calling
- Methods, Genotype Calling
- Genotype Determination Methods
- Determination Method, Genotype
- Determination Methods, Genotype
- Genotype Determination Method
- Method, Genotype Determination
- Methods, Genotype Determination
|
Below are MeSH descriptors whose meaning is more general than "Genotyping Techniques".
Below are MeSH descriptors whose meaning is more specific than "Genotyping Techniques".
This graph shows the total number of publications written about "Genotyping Techniques" by people in this website by year, and whether "Genotyping Techniques" 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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2011 | 2 | 0 | 2 |
2012 | 0 | 2 | 2 |
2013 | 2 | 2 | 4 |
2014 | 2 | 4 | 6 |
2015 | 5 | 1 | 6 |
2016 | 2 | 3 | 5 |
2017 | 4 | 1 | 5 |
2018 | 3 | 5 | 8 |
2019 | 1 | 3 | 4 |
2020 | 0 | 2 | 2 |
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Below are the most recent publications written about "Genotyping Techniques" by people in Profiles.
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Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk. Sci Rep. 2020 06 16; 10(1):9688.
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Epithelioid Trophoblastic Tumor: Expanding the Clinicopathologic Spectrum of a Rare Malignancy. Int J Gynecol Pathol. 2020 Jan; 39(1):8-18.
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Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. PLoS Genet. 2019 12; 15(12):e1008500.
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GraphTyper2 enables population-scale genotyping of structural variation using pangenome graphs. Nat Commun. 2019 11 27; 10(1):5402.
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A specific amino acid motif of HLA-DRB1 mediates risk and interacts with smoking history in Parkinson's disease. Proc Natl Acad Sci U S A. 2019 04 09; 116(15):7419-7424.
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Analytical validity of a genotyping assay for use with personalized antihypertensive and chronic kidney disease therapy. Pharmacogenet Genomics. 2019 01; 29(1):18-22.
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Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis. Lancet Respir Med. 2019 03; 7(3):227-238.
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Chronotype and cellular circadian rhythms predict the clinical response to lithium maintenance treatment in patients with bipolar disorder. Neuropsychopharmacology. 2019 02; 44(3):620-628.
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Genotyping Polyploids from Messy Sequencing Data. Genetics. 2018 11; 210(3):789-807.
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Genetic architecture of gene expression traits across diverse populations. PLoS Genet. 2018 08; 14(8):e1007586.