"Contig Mapping" 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.
Overlapping of cloned or sequenced DNA to construct a continuous region of a gene, chromosome or genome.
| Descriptor ID |
D020451
|
| MeSH Number(s) |
E05.393.183.620.160 E05.393.260
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Contig Mapping".
Below are MeSH descriptors whose meaning is more specific than "Contig Mapping".
This graph shows the total number of publications written about "Contig Mapping" by people in this website by year, and whether "Contig Mapping" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
| 2015 | 0 | 1 | 1 |
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Below are the most recent publications written about "Contig Mapping" by people in Profiles.
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STRONG: metagenomics strain resolution on assembly graphs. Genome Biol. 2021 07 26; 22(1):214.
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Genomic variation in microbial populations inhabiting the marine subseafloor at deep-sea hydrothermal vents. Nat Commun. 2017 10 24; 8(1):1114.
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Recovering complete and draft population genomes from metagenome datasets. Microbiome. 2016 Mar 08; 4:8.
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Divergent responses of viral and bacterial communities in the gut microbiome to dietary disturbances in mice. ISME J. 2016 May; 10(5):1217-27.
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Scaffolding low quality genomes using orthologous protein sequences. Bioinformatics. 2013 Jan 15; 29(2):160-5.
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The draft genome of the transgenic tropical fruit tree papaya (Carica papaya Linnaeus). Nature. 2008 Apr 24; 452(7190):991-6.
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The DNA sequence of the human X chromosome. Nature. 2005 Mar 17; 434(7031):325-37.
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An integrated genetic, radiation hybrid, physical and transcription map of a region of distal mouse chromosome 12, including an imprinted locus and the 'Legs at odd angles' (Loa) mutation. Gene. 2002 Jan 23; 283(1-2):71-82.
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Genomic and genetic definition of a functional human centromere. Science. 2001 Oct 05; 294(5540):109-15.
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Large-insert clone/STS contigs in Xq11-q12, spanning deletions in patients with androgen insensitivity and mental retardation. Genomics. 2000 May 15; 66(1):104-9.