"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 | 2 | 0 | 2 |
| 2018 | 0 | 1 | 1 |
| 2019 | 0 | 2 | 2 |
| 2020 | 0 | 1 | 1 |
| 2021 | 0 | 5 | 5 |
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Below are the most recent publications written about "Whole Genome Sequencing" by people in Profiles.
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The genomic origins of the Bronze Age Tarim Basin mummies. Nature. 2021 11; 599(7884):256-261.
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Tracing Transmission of Sin Nombre Virus and Discovery of Infection in Multiple Rodent Species. J Virol. 2021 11 09; 95(23):e0153421.
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Genomic and evolutionary classification of lung cancer in never smokers. Nat Genet. 2021 09; 53(9):1348-1359.
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Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease. Am J Hum Genet. 2021 03 04; 108(3):431-445.
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The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing. Nat Neurosci. 2021 02; 24(2):176-185.
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Cancer regulatory variation. Curr Opin Genet Dev. 2021 02; 66:41-49.
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Whole-Genome Sequencing to Detect Numerous Campylobacter jejuni Outbreaks and Match Patient Isolates to Sources, Denmark, 2015-2017. Emerg Infect Dis. 2020 03; 26(3):523-532.
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Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease. N Engl J Med. 2019 10 24; 381(17):1644-1652.
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Evaluation of the contribution of germline variants in BRCA1 and BRCA2 to uveal and cutaneous melanoma. Melanoma Res. 2019 10; 29(5):483-490.
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Statement on bioinformatics and capturing the benefits of genome sequencing for society. Hum Genomics. 2019 05 29; 13(1):24.