"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 |
|---|
| 1997 | 1 | 0 | 1 |
| 1998 | 1 | 1 | 2 |
| 2000 | 1 | 0 | 1 |
| 2001 | 2 | 0 | 2 |
| 2002 | 0 | 1 | 1 |
| 2004 | 4 | 1 | 5 |
| 2005 | 0 | 1 | 1 |
| 2006 | 1 | 1 | 2 |
| 2007 | 4 | 3 | 7 |
| 2008 | 1 | 5 | 6 |
| 2009 | 3 | 2 | 5 |
| 2010 | 4 | 3 | 7 |
| 2011 | 8 | 6 | 14 |
| 2012 | 6 | 3 | 9 |
| 2013 | 3 | 5 | 8 |
| 2014 | 3 | 4 | 7 |
| 2015 | 6 | 6 | 12 |
| 2016 | 5 | 3 | 8 |
| 2017 | 3 | 4 | 7 |
| 2018 | 3 | 6 | 9 |
| 2019 | 2 | 6 | 8 |
| 2020 | 2 | 1 | 3 |
| 2021 | 1 | 1 | 2 |
| 2024 | 1 | 3 | 4 |
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Below are the most recent publications written about "Genome, Human" by people in Profiles.
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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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Improved allele frequencies in gnomAD through local ancestry inference. Nat Commun. 2025 Oct 06; 16(1):8734.
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Toward ethical provenance tracking: The GA4GH model data access agreement (DAA). Genet Med. 2026 Jan; 28(1):101594.
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Coalescing single-cell genomes and transcriptomes to decode breast cancer progression. Cell. 2025 Oct 30; 188(22):6355-6369.e16.
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Structural Variants: Mechanisms, Mapping, and Interpretation in Human Genetics. Genes (Basel). 2025 Jul 29; 16(8).
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Mapping MAVE data for use in human genomics applications. Genome Biol. 2025 Jun 25; 26(1):179.
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A Hitchhiker's Guide to long-read genomic analysis. Genome Res. 2025 Apr 14; 35(4):545-558.
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Closing the gaps, and improving somatic structural variant analysis and benchmarking using CHM13-T2T. Genome Res. 2025 Apr 14; 35(4):621-631.
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Unraveling the hidden complexity of cancer through long-read sequencing. Genome Res. 2025 Apr 14; 35(4):599-620.