"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 |
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2016 | 6 | 2 | 8 |
2017 | 5 | 11 | 16 |
2018 | 11 | 16 | 27 |
2019 | 10 | 17 | 27 |
2020 | 16 | 26 | 42 |
2021 | 11 | 16 | 27 |
2022 | 0 | 20 | 20 |
2023 | 0 | 6 | 6 |
2024 | 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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Whole genome sequencing followed by functional analysis of genomic deletion encompassing ERCC8 and NDUFAF2 genes in a non-consanguineous Indian family reveals dysfunctional mitochondrial bioenergetics leading to infant mortality. Mitochondrion. 2024 Mar; 75:101844.
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Genomic characterization of the C. tuberculostearicum species complex, a prominent member of the human skin microbiome. mSystems. 2023 Dec 21; 8(6):e0063223.
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Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study. Am J Hum Genet. 2023 10 05; 110(10):1704-1717.
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Systematic assessment of the contribution of structural variants to inherited retinal diseases. Hum Mol Genet. 2023 06 05; 32(12):2005-2015.
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The landscape of tolerated genetic variation in humans and primates. Science. 2023 06 02; 380(6648):eabn8153.
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The genomic landscape of familial glioma. Sci Adv. 2023 04 28; 9(17):eade2675.
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Novel Pathogenic Mutations Identified from Whole-Genome Sequencing in Unsolved Cases of Patients Affected with Inherited Retinal Diseases. Genes (Basel). 2023 02 09; 14(2).
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Genome-Wide Analysis of Structural Variants in Parkinson Disease. Ann Neurol. 2023 05; 93(5):1012-1022.
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Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies. Nat Genet. 2023 01; 55(1):154-164.
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Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program. Nat Commun. 2022 12 08; 13(1):7592.