"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.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2016 | 5 | 0 | 5 |
| 2017 | 5 | 9 | 14 |
| 2018 | 12 | 12 | 24 |
| 2019 | 10 | 11 | 21 |
| 2020 | 13 | 19 | 32 |
| 2021 | 7 | 14 | 21 |
| 2022 | 0 | 18 | 18 |
| 2023 | 0 | 5 | 5 |
| 2024 | 10 | 7 | 17 |
| 2025 | 1 | 2 | 3 |
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Below are the most recent publications written about "Whole Genome Sequencing" by people in Profiles.
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Unveiling the Genetic Landscape of Coronary Artery Disease Through Common and Rare Structural Variants. J Am Heart Assoc. 2025 Feb 18; 14(4):e036499.
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A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. Nat Comput Sci. 2025 Feb; 5(2):125-143.
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Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood. Am J Hum Genet. 2025 Feb 06; 112(2):276-290.
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Leveraging the T2T assembly to resolve rare and pathogenic inversions in reference genome gaps. Genome Res. 2024 Nov 20; 34(11):1785-1797.
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The "genetic test request": A genomic stewardship intervention for inpatient exome and genome orders at a tertiary pediatric hospital. Genet Med. 2025 Feb; 27(2):101330.
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Association of common and rare variants with Alzheimer's disease in more than 13,000 diverse individuals with whole-genome sequencing from the Alzheimer's Disease Sequencing Project. Alzheimers Dement. 2024 Dec; 20(12):8470-8483.
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Rare variant contribution to the heritability of coronary artery disease. Nat Commun. 2024 Oct 09; 15(1):8741.
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Whole-genome sequencing in 333,100 individuals reveals rare non-coding single variant and aggregate associations with height. Nat Commun. 2024 Oct 03; 15(1):8549.
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Prevalence of the cefazolin inoculum effect (CzIE) in nasal colonizing methicillin-susceptible Staphylococcus aureus in patients from intensive care units in Colombia and use of a modified rapid nitrocefin test for detection. Antimicrob Agents Chemother. 2024 11 06; 68(11):e0089824.
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Exploring the complexity of systemic sclerosis etiology by trio whole genome sequencing. Hum Mol Genet. 2024 09 19; 33(19):1643-1647.