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  2. Karyotype - Wikipedia

    en.wikipedia.org/wiki/Karyotype

    [1] [2] Karyotyping is the process by which a karyotype is discerned by determining the chromosome complement of an individual, including the number of chromosomes and any abnormalities. Micrographic karyogram of human male using Giemsa staining Schematic karyogram demonstrating the basic knowledge needed to read a karyotype

  3. International System for Human Cytogenomic Nomenclature

    en.wikipedia.org/wiki/International_System_for...

    Three chromosomal abnormalities with ISCN nomenclature, with increasing complexity: (A) A tumour karyotype in a male with loss of the Y chromosome, (B) Prader–Willi Syndrome i.e. deletion in the 15q11-q12 region and (C) an arbitrary karyotype that involves a variety of autosomal and allosomal abnormalities. [3]

  4. Polysomy - Wikipedia

    en.wikipedia.org/wiki/Polysomy

    Spectral karyotyping (SKY) looks at the entire karyotype by using fluorescent labels and assigning a particular color to each chromosome. SKY is usually performed after conventional cytogenic techniques have already detected an abnormal chromosome. FISH analysis is then used to confirm the identity of the chromosome. [50]

  5. Fluorescence in situ hybridization - Wikipedia

    en.wikipedia.org/wiki/Fluorescence_in_situ...

    Spectral karyotyping is an image of colored chromosomes. Spectral karyotyping involves FISH using multiple forms of many types of probes with the result to see each chromosome labeled through its metaphase stage. This type of karyotyping is used specifically when seeking out chromosome arrangements.

  6. Applied Spectral Imaging - Wikipedia

    en.wikipedia.org/wiki/Applied_Spectral_Imaging

    ASI's clinical applications for laboratories include the scoring of chromosome analysis and karyotyping, fluorescent karyotyping, spectral karyotyping, karyotyping of multiple species, scanning and detection of metaphases and interphases, FISH review and analysis, matching of tissue FISH with H&E/ IHC, Brightfield whole slide imaging, IHC ...

  7. G banding - Wikipedia

    en.wikipedia.org/wiki/G_banding

    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 ...

  8. Cytogenetic notation - Wikipedia

    en.wikipedia.org/wiki/Cytogenetic_notation

    Precedes karyotype results from FISH analysis mar: Marker chromosome: mat: Maternally-derived chromosome rearrangement p: Short arm of a chromosome pat: Paternally-derived chromosome rearrangement psu dic: pseudo dicentric – only one centromere in a dicentric chromosome is active q: Long arm of a chromosome r: Ring chromosome t: Translocation ...

  9. Giemsa stain - Wikipedia

    en.wikipedia.org/wiki/Giemsa_stain

    Giemsa stained Trypanosoma parasites (Chagas disease pathogen) Whirling disease section stained with Giemsa stain. Giemsa stain (/ ˈ ɡ iː m z ə /), named after German chemist and bacteriologist Gustav Giemsa, is a nucleic acid stain used in cytogenetics and for the histopathological diagnosis of malaria and other parasites.