"Whole Exome 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 complete complement of sequences of all EXONS of an organism or individual.
| Descriptor ID |
D000073359
|
| MeSH Number(s) |
E05.393.760.700.825.500
|
| Concept/Terms |
Whole Exome Sequencing- Whole Exome Sequencing
- Exome Sequencing, Whole
- Exome Sequencings, Whole
- Sequencing, Whole Exome
- Sequencings, Whole Exome
- Whole Exome Sequencings
- Complete Exome Sequencing
- Complete Exome Sequencings
- Exome Sequencing, Complete
- Exome Sequencings, Complete
- Sequencing, Complete Exome
- Sequencings, Complete Exome
Whole Transcriptome Sequencing- Whole Transcriptome Sequencing
- Sequencing, Whole Transcriptome
- Sequencings, Whole Transcriptome
- Transcriptome Sequencing, Whole
- Transcriptome Sequencings, Whole
- Whole Transcriptome Sequencings
- Complete Transcriptome Sequencing
- Complete Transcriptome Sequencings
- Sequencing, Complete Transcriptome
- Sequencings, Complete Transcriptome
- Transcriptome Sequencing, Complete
- Transcriptome Sequencings, Complete
|
Below are MeSH descriptors whose meaning is more general than "Whole Exome Sequencing".
Below are MeSH descriptors whose meaning is more specific than "Whole Exome Sequencing".
This graph shows the total number of publications written about "Whole Exome Sequencing" by people in this website by year, and whether "Whole Exome Sequencing" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2017 | 11 | 16 | 27 |
| 2018 | 12 | 43 | 55 |
| 2019 | 1 | 11 | 12 |
| 2020 | 1 | 5 | 6 |
| 2021 | 1 | 3 | 4 |
To return to the timeline, click here.
Below are the most recent publications written about "Whole Exome Sequencing" by people in Profiles.
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scAdapt: virtual adversarial domain adaptation network for single cell RNA-seq data classification across platforms and species. Brief Bioinform. 2021 11 05; 22(6).
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Autophagy and Mitophagy-Related Pathways at the Crossroads of Genetic Pathways Involved in Familial Sarcoidosis and Host-Pathogen Interactions Induced by Coronaviruses. Cells. 2021 08 05; 10(8).
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Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19. J Clin Invest. 2021 07 15; 131(14).
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Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. Am J Hum Genet. 2021 07 01; 108(7):1350-1355.
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Regulatory Noncoding and Predicted Pathogenic Coding Variants of CCR5 Predispose to Severe COVID-19. Int J Mol Sci. 2021 May 20; 22(10).
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Detection of SARS-CoV-2 genome and whole transcriptome sequencing in frontal cortex of COVID-19 patients. Brain Behav Immun. 2021 10; 97:13-21.
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Robust Antibody and T Cell Responses to SARS-CoV-2 in Patients with Antibody Deficiency. J Clin Immunol. 2021 08; 41(6):1146-1153.
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Analysis workflow of publicly available RNA-sequencing datasets. STAR Protoc. 2021 06 18; 2(2):100478.
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Whole-Transcriptome RNA Sequencing Reveals Significant Differentially Expressed mRNAs, miRNAs, and lncRNAs and Related Regulating Biological Pathways in the Peripheral Blood of COVID-19 Patients. Mediators Inflamm. 2021; 2021:6635925.
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Variants in ACE2 and TMPRSS2 Genes Are Not Major Determinants of COVID-19 Severity in UK Biobank Subjects. Hum Hered. 2020; 85(2):66-68.