"INDEL Mutation" 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.
A mutation named with the blend of insertion and deletion. It refers to a length difference between two ALLELES where it is unknowable if the difference was originally caused by a SEQUENCE INSERTION or by a SEQUENCE DELETION. If the number of nucleotides in the insertion/deletion is not divisible by three, and it occurs in a protein coding region, it is also a FRAMESHIFT MUTATION.
| Descriptor ID |
D054643
|
| MeSH Number(s) |
G05.365.590.500 G05.558.370
|
| Concept/Terms |
INDEL Mutation- INDEL Mutation
- INDEL Mutations
- Mutation, INDEL
- Mutations, INDEL
- Insertion-Deletion Mutation
- Insertion Deletion Mutation
- Insertion-Deletion Mutations
- Mutation, Insertion-Deletion
- Mutations, Insertion-Deletion
|
Below are MeSH descriptors whose meaning is more general than "INDEL Mutation".
Below are MeSH descriptors whose meaning is more specific than "INDEL Mutation".
This graph shows the total number of publications written about "INDEL Mutation" by people in this website by year, and whether "INDEL Mutation" 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 |
|---|
| 2009 | 1 | 1 | 2 |
| 2010 | 0 | 2 | 2 |
| 2011 | 0 | 3 | 3 |
| 2012 | 0 | 2 | 2 |
| 2013 | 2 | 0 | 2 |
| 2014 | 0 | 1 | 1 |
| 2015 | 1 | 1 | 2 |
| 2016 | 0 | 1 | 1 |
| 2017 | 1 | 1 | 2 |
| 2018 | 0 | 3 | 3 |
| 2020 | 0 | 2 | 2 |
| 2021 | 0 | 3 | 3 |
| 2022 | 0 | 2 | 2 |
| 2024 | 0 | 1 | 1 |
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Below are the most recent publications written about "INDEL Mutation" by people in Profiles.
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Diversity of ribosomes at the level of rRNA variation associated with human health and disease. Cell Genom. 2024 Sep 11; 4(9):100629.
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Single-neuron whole genome sequencing identifies increased somatic mutation burden in Alzheimer's disease related genes. Neurobiol Aging. 2023 03; 123:222-232.
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The sequences of 150,119 genomes in the UK Biobank. Nature. 2022 07; 607(7920):732-740.
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Next-Generation Sequencing Concordance Analysis of Comprehensive Solid Tumor Profiling between a Centralized Specialty Laboratory and the Decentralized Personal Genome Diagnostics elio Tissue Complete Kitted Solution. J Mol Diagn. 2021 10; 23(10):1324-1333.
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Clinical Validation of Whole Genome Sequencing for Cancer Diagnostics. J Mol Diagn. 2021 07; 23(7):816-833.
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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program. Nature. 2021 Feb; 590(7845):290-299.
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Synthetic CRISPR/Cas9 reagents facilitate genome editing and homology directed repair. Nucleic Acids Res. 2020 04 17; 48(7):e38.
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Analyses of non-coding somatic drivers in 2,658 cancer whole genomes. Nature. 2020 02; 578(7793):102-111.
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Hybrid Capture-Based Genomic Profiling of Circulating Tumor DNA from Patients with Advanced Non-Small Cell Lung Cancer. J Thorac Oncol. 2019 02; 14(2):255-264.
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The landscape of epilepsy-related GATOR1 variants. Genet Med. 2019 02; 21(2):398-408.