"Whole Genome Sequencing" 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.
Techniques to determine the entire sequence of the GENOME of an organism or individual.
| Descriptor ID |
D000073336
|
| MeSH Number(s) |
E05.393.760.700.825
|
| Concept/Terms |
Whole Genome Sequencing- Whole Genome Sequencing
- Genome Sequencing, Whole
- Sequencing, Whole Genome
- Complete Genome Sequencing
- Genome Sequencing, Complete
- Sequencing, Complete Genome
|
Below are MeSH descriptors whose meaning is more general than "Whole Genome Sequencing".
Below are MeSH descriptors whose meaning is more specific than "Whole Genome Sequencing".
This graph shows the total number of publications written about "Whole Genome Sequencing" by people in this website by year, and whether "Whole Genome Sequencing" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2019 | 1 | 1 | 2 |
| 2021 | 0 | 1 | 1 |
| 2022 | 0 | 1 | 1 |
| 2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Whole Genome Sequencing" by people in Profiles.
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Assessment and validation of enrichment and target capture approaches to improve Mycobacterium tuberculosis WGS from direct patient samples. J Clin Microbiol. 2023 10 24; 61(10):e0038223.
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Association of mRNA Vaccination With Clinical and Virologic Features of COVID-19 Among US Essential and Frontline Workers. JAMA. 2022 10 18; 328(15):1523-1533.
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Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. Am J Hum Genet. 2021 10 07; 108(10):1836-1851.
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Integrating Personalized Medicine With Population Health Management: The Path Forward. JAMA. 2020 Aug 18; 324(7):631-632.
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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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Cumulative Burden of Colorectal Cancer-Associated Genetic Variants Is More Strongly Associated With Early-Onset vs Late-Onset Cancer. Gastroenterology. 2020 04; 158(5):1274-1286.e12.
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The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations. Am J Hum Genet. 2018 09 06; 103(3):319-327.
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Approaches to carrier testing and results disclosure in translational genomics research: The clinical sequencing exploratory research consortium experience. Mol Genet Genomic Med. 2018 11; 6(6):898-909.
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Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory. Am J Hum Genet. 2018 06 07; 102(6):1078-1089.