"Genome, Human" 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.
The complete genetic complement contained in the DNA of a set of CHROMOSOMES in a HUMAN. The length of the human genome is about 3 billion base pairs.
| Descriptor ID |
D015894
|
| MeSH Number(s) |
G05.360.340.350
|
| Concept/Terms |
Genome, Human- Genome, Human
- Human Genome
- Genomes, Human
- Human Genomes
|
Below are MeSH descriptors whose meaning is more general than "Genome, Human".
Below are MeSH descriptors whose meaning is more specific than "Genome, Human".
This graph shows the total number of publications written about "Genome, Human" by people in this website by year, and whether "Genome, Human" 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 |
|---|
| 1996 | 1 | 0 | 1 |
| 1997 | 2 | 2 | 4 |
| 1998 | 4 | 2 | 6 |
| 1999 | 2 | 1 | 3 |
| 2000 | 2 | 1 | 3 |
| 2001 | 7 | 5 | 12 |
| 2002 | 3 | 7 | 10 |
| 2003 | 9 | 6 | 15 |
| 2004 | 12 | 7 | 19 |
| 2005 | 3 | 5 | 8 |
| 2006 | 13 | 15 | 28 |
| 2007 | 24 | 6 | 30 |
| 2008 | 14 | 15 | 29 |
| 2009 | 8 | 14 | 22 |
| 2010 | 21 | 11 | 32 |
| 2011 | 20 | 24 | 44 |
| 2012 | 24 | 21 | 45 |
| 2013 | 14 | 24 | 38 |
| 2014 | 16 | 15 | 31 |
| 2015 | 32 | 17 | 49 |
| 2016 | 19 | 13 | 32 |
| 2017 | 14 | 17 | 31 |
| 2018 | 23 | 19 | 42 |
| 2019 | 18 | 17 | 35 |
| 2020 | 16 | 16 | 32 |
| 2021 | 15 | 22 | 37 |
| 2022 | 14 | 5 | 19 |
| 2023 | 8 | 5 | 13 |
| 2024 | 13 | 14 | 27 |
| 2025 | 11 | 12 | 23 |
| 2026 | 5 | 3 | 8 |
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Below are the most recent publications written about "Genome, Human" by people in Profiles.
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ClinGen API platform for classification of human genetic variants. Cell Genom. 2026 Apr 08; 6(4):101211.
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Comparison of variant callers using 60?532 multi-ancestry whole genome sequences. Brief Bioinform. 2026 Mar 01; 27(2).
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Phenome-wide analysis of copy number variants in 470,727 UK Biobank genomes. Nature. 2026 04; 652(8110):675-685.
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Using the linear references from the pangenome to discover missing autism variants. Nat Commun. 2026 Jan 23; 17(1):1681.
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Resolution of a human chromosomal mystery: Evolutionary complexity revealed. Cell Genom. 2026 Jan 14; 6(1):101135.
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The biomedical landscape of genomic structural variation in the qatari population. Nat Commun. 2026 Jan 13; 17(1):1019.
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VACmap: an accurate long-read aligner for unraveling complex genomic rearrangements. Nat Commun. 2026 Jan 05; 16(1):11198.
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Whole-Genome Amplification on Single Circulating Trophoblast Cell. Methods Mol Biol. 2026; 3003:11-23.
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cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions. Nat Methods. 2026 Feb; 23(2):338-349.
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Single cell long read whole genome sequencing reveals somatic transposon activity in human brain. Commun Biol. 2025 Nov 20; 8(1):1627.