"HapMap Project" 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 coordinated international effort to identify and catalog patterns of linked variations (HAPLOTYPES) found in the human genome across the entire human population.
| Descriptor ID |
D060148
|
| MeSH Number(s) |
H01.158.273.180.350.162 H01.158.273.343.249.199 H01.158.273.343.350.130 H01.158.273.343.385.750 H01.770.644.145.350.249
|
| Concept/Terms |
HapMap Project- HapMap Project
- HapMap Projects
- Project, HapMap
- Projects, HapMap
- International HapMap Project
- HapMap Project, International
- HapMap Projects, International
- International HapMap Projects
- Project, International HapMap
- Projects, International HapMap
HapMap- HapMap
- Human Haplotype Map
- Haplotype Map, Human
- Haplotype Maps, Human
- Human Haplotype Maps
- Map, Human Haplotype
- Maps, Human Haplotype
|
Below are MeSH descriptors whose meaning is more general than "HapMap Project".
Below are MeSH descriptors whose meaning is more specific than "HapMap Project".
This graph shows the total number of publications written about "HapMap Project" by people in this website by year, and whether "HapMap Project" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 0 | 2 | 2 |
| 2012 | 1 | 4 | 5 |
| 2013 | 0 | 2 | 2 |
| 2015 | 1 | 0 | 1 |
| 2016 | 0 | 1 | 1 |
| 2020 | 0 | 1 | 1 |
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "HapMap Project" by people in Profiles.
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BMI-CNV: a Bayesian framework for multiple genotyping platforms detection of copy number variants. Genetics. 2022 11 30; 222(4).
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Joint modeling of eQTLs and parent-of-origin effects using an orthogonal framework with RNA-seq data. Hum Genet. 2020 Aug; 139(8):1107-1117.
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HLA Haplotypes In 250 Families: The Baylor Laboratory Results And A Perspective On A Core NGS Testing Model For The 17th International HLA And Immunogenetics Workshop. Hum Immunol. 2019 Nov; 80(11):897-905.
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FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data. BMC Bioinformatics. 2016 Mar 09; 17:122.
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Addressing population-specific multiple testing burdens in genetic association studies. Ann Hum Genet. 2015 Mar; 79(2):136-47.
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RRM1 and RRM2 pharmacogenetics: association with phenotypes in HapMap cell lines and acute myeloid leukemia patients. Pharmacogenomics. 2013 Sep; 14(12):1449-66.
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A linkage disequilibrium-based approach to selecting disease-associated rare variants. PLoS One. 2013; 8(7):e69226.
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Next-generation sequencing of human mitochondrial reference genomes uncovers high heteroplasmy frequency. PLoS Comput Biol. 2012; 8(10):e1002737.
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Comprehensive evaluation of imputation performance in African Americans. J Hum Genet. 2012 Jul; 57(7):411-21.
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Relax with CouchDB--into the non-relational DBMS era of bioinformatics. Genomics. 2012 Jul; 100(1):1-7.