Physical Chromosome Mapping
"Physical Chromosome 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.
Mapping of the linear order of genes on a chromosome with units indicating their distances by using methods other than genetic recombination. These methods include nucleotide sequencing, overlapping deletions in polytene chromosomes, and electron micrography of heteroduplex DNA. (From King & Stansfield, A Dictionary of Genetics, 5th ed)
|Physical Chromosome Mapping
- Physical Chromosome Mapping
- Physical Mapping (Genetics)
- Physical Mappings (Genetics)
- Chromosome Mapping, Physical
- Chromosome Mappings, Physical
- Mapping, Physical Chromosome
- Mappings, Physical Chromosome
- Physical Chromosome Mappings
Below are MeSH descriptors whose meaning is more general than "Physical Chromosome Mapping".
Below are MeSH descriptors whose meaning is more specific than "Physical Chromosome Mapping".
This graph shows the total number of publications written about "Physical Chromosome Mapping" by people in this website by year, and whether "Physical Chromosome Mapping" was a major or minor topic of these publications.
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Below are the most recent publications written about "Physical Chromosome Mapping" by people in Profiles.
A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response. Nat Genet. 2021 10; 53(10):1504-1516.
Fine-mapping QTLs in advanced intercross lines and other outbred populations. Mamm Genome. 2014 Aug; 25(7-8):271-92.
Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene. Psychiatr Genet. 2013 Feb; 23(1):11-9.
Construction of physical maps for the sex-specific regions of papaya sex chromosomes. BMC Genomics. 2012 May 08; 13:176.
Construction of papaya male and female BAC libraries and application in physical mapping of the sex chromosomes. J Biomed Biotechnol. 2011; 2011:929472.
Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7q. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar; 156(2):168-76.
Detailed analysis of a contiguous 22-Mb region of the maize genome. PLoS Genet. 2009 Nov; 5(11):e1000728.
Autosomal-dominant retinitis pigmentosa caused by a mutation in SNRNP200, a gene required for unwinding of U4/U6 snRNAs. Am J Hum Genet. 2009 Nov; 85(5):617-27.
FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation. Nat Genet. 2009 Sep; 41(9):1037-42.
Comparative genomic analysis and evolution of the T cell receptor loci in the opossum Monodelphis domestica. BMC Genomics. 2008 Feb 29; 9:111.