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G-banding, G banding or Giemsa banding is a technique used in cytogenetics to produce a visible karyotype by staining condensed chromosomes. It is the most common chromosome banding method. [ 1 ] It is useful for identifying genetic diseases (mainly chromosomal abnormalities ) through the photographic representation of the entire chromosome ...
Chromosomes display a banded pattern when treated with some stains. Bands are alternating light and dark stripes that appear along the lengths of chromosomes. Unique banding patterns are used to identify chromosomes and to diagnose chromosomal aberrations, including chromosome breakage, loss, duplication, translocation or inverted segments.
A metaphase cell positive for the BCR/ABL rearrangement using FISH. Cytogenetics is essentially a branch of genetics, but is also a part of cell biology/cytology (a subdivision of human anatomy), that is concerned with how the chromosomes relate to cell behaviour, particularly to their behaviour during mitosis and meiosis. [1]
The list of organisms by chromosome count describes ploidy or numbers of chromosomes in the cells of various plants, animals, protists, and other living organisms. This number, along with the visual appearance of the chromosome, is known as the karyotype , [ 1 ] [ 2 ] [ 3 ] and can be found by looking at the chromosomes through a microscope .
Cytogenetic banding nomenclature. The shorter arm of a chromosome is termed the p arm or p-arm, while the longer arm is the q arm or q-arm. The chromosomal locus of a typical gene, for example, might be written 3p22.1, where: [citation needed] 3 = chromosome 3; p = p-arm; 22 = region 2, band 2 (read as "two, two", not "twenty-two") 1 = sub-band 1
It shows 22 homologous autosomal chromosome pairs, both the female (XX) and male (XY) versions of the two sex chromosomes, as well as the mitochondrial genome (at bottom left). In genetics , a chromosomal rearrangement is a mutation that is a type of chromosome abnormality involving a change in the structure of the native chromosome . [ 1 ]
There are two distinctive mapping approaches used in the field of genome mapping: genetic maps (also known as linkage maps) [7] and physical maps. [3] While both maps are a collection of genetic markers and gene loci, [8] genetic maps' distances are based on the genetic linkage information, while physical maps use actual physical distances usually measured in number of base pairs.
G-banding patterns of human chromosome 1 in three different resolutions (400, [14] 550 [15] and 850 [3]). Band length in this diagram is based on the ideograms from ISCN (2013). [ 16 ] This type of ideogram represents actual relative band length observed under a microscope at the different moments during the mitotic process .