 Genotyping Techniques
"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
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| MeSH Number(s) |
E05.393.442
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| 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
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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 |
|---|
| 2011 | 0 | 1 | 1 | | 2012 | 1 | 0 | 1 | | 2013 | 2 | 0 | 2 | | 2014 | 1 | 1 | 2 | | 2015 | 1 | 0 | 1 | | 2017 | 1 | 2 | 3 | | 2018 | 1 | 0 | 1 | | 2019 | 1 | 2 | 3 | | 2020 | 1 | 0 | 1 | | 2021 | 1 | 3 | 4 | | 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Genotyping Techniques" by people in Profiles.
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Pratt VM, Cavallari LH, Fulmer ML, Gaedigk A, Hachad H, Ji Y, Kalman LV, Ly RC, Moyer AM, Scott SA, Turner AJ, van Schaik RHN, Whirl-Carrillo M, Weck KE. DPYD Genotyping Recommendations: A Joint Consensus Recommendation of the Association for Molecular Pathology, American College of Medical Genetics and Genomics, Clinical Pharmacogenetics Implementation Consortium, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, European Society for Pharmacogenomics and Personalized Therapy, Pharmacogenomics Knowledgebase, and Pharmacogene Variation Consortium. J Mol Diagn. 2024 Oct; 26(10):851-863.
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Mehta RS, Taylor ZL, Martin LJ, Rosen MJ, Ramsey LB. SLCO1B1 *15 allele is associated with methotrexate-induced nausea in pediatric patients with inflammatory bowel disease. Clin Transl Sci. 2022 01; 15(1):63-69.
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Pratt VM, Cavallari LH, Del Tredici AL, Gaedigk A, Hachad H, Ji Y, Kalman LV, Ly RC, Moyer AM, Scott SA, van Schaik RHN, Whirl-Carrillo M, Weck KE. Recommendations for Clinical CYP2D6 Genotyping Allele Selection: A Joint Consensus Recommendation of the Association for Molecular Pathology, College of American Pathologists, Dutch Pharmacogenetics Working Group of the Royal Dutch Pharmacists Association, and the European Society for Pharmacogenomics and Personalized Therapy. J Mol Diagn. 2021 09; 23(9):1047-1064.
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Pratt VM, Turner A, Broeckel U, Dawson DB, Gaedigk A, Lynnes TC, Medeiros EB, Moyer AM, Requesens D, Vetrini F, Kalman LV. Characterization of Reference Materials with an Association for Molecular Pathology Pharmacogenetics Working Group Tier 2 Status: CYP2C9, CYP2C19, VKORC1, CYP2C Cluster Variant, and GGCX: A GeT-RM Collaborative Project. J Mol Diagn. 2021 08; 23(8):952-958.
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Hongkaew Y, Wang WY, Gaedigk R, Sukasem C, Gaedigk A. Resolving discordant CYP2D6 genotyping results in Thai subjects: platform limitations and novel haplotypes. Pharmacogenomics. 2021 06; 22(9):529-541.
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Casto AM, Stout SC, Selvarangan R, Freeman AF, Newell BD, Stahl ED, Ahmed AA, Greninger AL, Yin DE. Evaluation of Genotypic Antiviral Resistance Testing as an Alternative to Phenotypic Testing in a Patient with DOCK8 Deficiency and Severe HSV-1 Disease. J Infect Dis. 2020 06 11; 221(12):2035-2042.
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Hassan F, Kanwar N, Harrison CJ, Halasa NB, Chappell JD, Englund JA, Klein EJ, Weinberg GA, Szilagyi PG, Moffatt ME, Oberste MS, Nix WA, Rogers S, Bowen MD, Vinj? J, Wikswo ME, Parashar UD, Payne DC, Selvarangan R. Viral Etiology of Acute Gastroenteritis in <2-Year-Old US Children in the Post-Rotavirus Vaccine Era. J Pediatric Infect Dis Soc. 2019 Nov 06; 8(5):414-421.
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Gaedigk A, Turner A, Everts RE, Scott SA, Aggarwal P, Broeckel U, McMillin GA, Melis R, Boone EC, Pratt VM, Kalman LV. Characterization of Reference Materials for Genetic Testing of CYP2D6 Alleles: A GeT-RM Collaborative Project. J Mol Diagn. 2019 11; 21(6):1034-1052.
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Hachad H, Ramsey LB, Scott SA. Interpreting and Implementing Clinical Pharmacogenetic Tests: Perspectives From Service Providers. Clin Pharmacol Ther. 2019 08; 106(2):298-301.
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Lee SB, Wheeler MM, Patterson K, McGee S, Dalton R, Woodahl EL, Gaedigk A, Thummel KE, Nickerson DA. Stargazer: a software tool for calling star alleles from next-generation sequencing data using CYP2D6 as a model. Genet Med. 2019 02; 21(2):361-372.
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