"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.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2019 | 0 | 2 | 2 |
| 2020 | 0 | 3 | 3 |
| 2021 | 0 | 2 | 2 |
| 2022 | 0 | 2 | 2 |
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Below are the most recent publications written about "Whole Exome Sequencing" by people in Profiles.
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Isolating and cryopreserving pig skin cells for single-cell RNA sequencing study. PLoS One. 2022; 17(2):e0263869.
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Integrated Analysis of Coexpression and Exome Sequencing to Prioritize Susceptibility Genes for Familial Cutaneous Melanoma. J Invest Dermatol. 2022 09; 142(9):2464-2475.e5.
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Determinants of anti-PD-1 response and resistance in clear cell renal cell carcinoma. Cancer Cell. 2021 11 08; 39(11):1497-1518.e11.
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Poroid adnexal skin tumors with YAP1 fusions exhibit similar histopathologic features: A series of six YAP1-rearranged adnexal skin tumors. J Cutan Pathol. 2021 Sep; 48(9):1139-1149.
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Novel compound heterozygous variants in the NBAS gene in a child with osteogenesis imperfecta and recurrent acute liver failure. BMJ Case Rep. 2021 Feb 04; 14(2).
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Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia. Genet Med. 2021 05; 23(5):881-887.
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Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science. Genet Med. 2021 02; 23(2):259-271.
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Recent advances in sarcoidosis genomics: epigenetics, gene expression, and gene by environment (G?×?E) interaction studies. Curr Opin Pulm Med. 2020 09; 26(5):544-553.
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Molecular subtyping in pancreatic neuroendocrine neoplasms: New insights into clinical, pathological unmet needs and challenges. Biochim Biophys Acta Rev Cancer. 2020 08; 1874(1):188367.
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A rare missense variant in the milk fat globule-EGF factor 8 (MFGE8) increases T2DM susceptibility and cardiovascular disease risk with population-specific effects. Acta Diabetol. 2020 Jun; 57(6):733-741.