"Exome" 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.
That part of the genome that corresponds to the complete complement of EXONS of an organism or cell.
Descriptor ID |
D059472
|
MeSH Number(s) |
G05.360.340.011
|
Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Exome".
Below are MeSH descriptors whose meaning is more specific than "Exome".
This graph shows the total number of publications written about "Exome" by people in this website by year, and whether "Exome" 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 |
---|
2011 | 6 | 3 | 9 |
2012 | 9 | 15 | 24 |
2013 | 14 | 20 | 34 |
2014 | 18 | 25 | 43 |
2015 | 19 | 36 | 55 |
2016 | 28 | 58 | 86 |
2017 | 13 | 30 | 43 |
2018 | 9 | 31 | 40 |
2019 | 7 | 24 | 31 |
2020 | 6 | 12 | 18 |
2021 | 10 | 9 | 19 |
2022 | 10 | 12 | 22 |
2023 | 4 | 7 | 11 |
2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "Exome" by people in Profiles.
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Genetic architecture and biology of youth-onset type 2 diabetes. Nat Metab. 2024 Feb; 6(2):226-237.
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Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child? Genet Med. 2024 Feb; 26(2):101033.
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Intestinal-Type Adenocarcinoma in Head and Neck: Dissecting Oncogenic Gene Alterations Through Whole Transcriptome and Exome Analysis. Mod Pathol. 2024 Jan; 37(1):100372.
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Rare variant associations with plasma protein levels in the UK Biobank. Nature. 2023 Oct; 622(7982):339-347.
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Beyond the exome: What's next in diagnostic testing for Mendelian conditions. Am J Hum Genet. 2023 08 03; 110(8):1229-1248.
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Discordant calls across genotype discovery approaches elucidate variants with systematic errors. Genome Res. 2023 06; 33(6):999-1005.
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Simple combination of multiple somatic variant callers to increase accuracy. Sci Rep. 2023 05 25; 13(1):8463.
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Exome sequence analysis of rare frequency variants in Late-Onset Alzheimer Disease. Metab Brain Dis. 2023 08; 38(6):2025-2036.
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Clinical Untargeted Metabolomics as a Functional Screen to Improve Variant Classification. Curr Protoc. 2023 Apr; 3(4):e720.
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Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants. Am J Med Genet A. 2023 06; 191(6):1546-1556.