"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 |
|---|
| 2017 | 0 | 2 | 2 |
| 2018 | 1 | 3 | 4 |
| 2019 | 2 | 5 | 7 |
| 2020 | 2 | 2 | 4 |
| 2021 | 0 | 6 | 6 |
| 2022 | 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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Identification of genome edited cells using CRISPRnano. Nucleic Acids Res. 2022 07 05; 50(W1):W199-W203.
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The native cistrome and sequence motif families of the maize ear. PLoS Genet. 2021 08; 17(8):e1009689.
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Genome sequencing in families with congenital limb malformations. Hum Genet. 2021 Aug; 140(8):1229-1239.
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New euchromatic variant dup(11)(p15.3p15.1) transmitted through two generations defined by low coverage whole genome sequencing. Am J Med Genet A. 2021 10; 185(10):3053-3056.
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Low Threshold for Cutaneous Allergen Sensitization but No Spontaneous Dermatitis or Atopy in FLG-Deficient Mice. J Invest Dermatol. 2021 11; 141(11):2611-2619.e2.
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Genomic surveillance of SARS-CoV-2 in the Republic of Congo. Int J Infect Dis. 2021 Apr; 105:735-738.
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Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation. PLoS Comput Biol. 2021 02; 17(2):e1007784.
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Gamete binning: chromosome-level and haplotype-resolved genome assembly enabled by high-throughput single-cell sequencing of gamete genomes. Genome Biol. 2020 12 29; 21(1):306.
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Ultra-rapid emergency genomic diagnosis of Donahue syndrome in a preterm infant within 17?hours. Am J Med Genet A. 2021 01; 185(1):90-96.
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The exhaustive genomic scan approach, with an application to rare-variant association analysis. Eur J Hum Genet. 2020 09; 28(9):1283-1291.
MeSH information
