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FISH article

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Total cards: 24•Content version: v4•Public deck•Updated: 8/1/2026

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#1
Front (Question)

multicolor FISH assay for detection of chromosomal abnormalities in sperm cells

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Centromere-FISH

#2
Front (Question)

42-color M-FISH variant that allows the detection of chromosomal abnormalities in the p- and q-arms of all 24 human chromosomes, except the p-arm of the Y and acrocentric chromosomes

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armFISH

#3
Front (Question)

very useful for detection, identification, and quantification of microorganisms involved in bioleaching processes

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Catalyzed Reporter Deposition-FISH (CARD-FISH)

#4
Front (Question)

used to determine the interactions of neuronal populations associated with different behaviors

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Cellular Compartment Analysis of Temporal (Cat) Activity by Fish (catFISH)

#5
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involves hybridization on binucleated cells in which cytokinesis has been blocked by treatment with cytochalasin B (CB)

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Cytochalasin B (CB-FISH)

#6
Front (Question)

allows to determine the relative orientation of two or more DNA sequences along a chromosome; useful in assessing chromosomal translocations and inversions

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Chromosome Orientation (CO)-FISH

#7
Front (Question)

enables recognition of all human chromosome arms on the basis of color and mapping of gene and viral integration site in the context of chromosome arm painting

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Combined Binary Ratio (COBRA)-FISH

#8
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This protocol is similar to CO-FISH except for the information about the directional organization of telomeric sequences.

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Chromosome Orientation and Direction (COD)-FISH

#9
Front (Question)

used for specific labeling of genomic sites. It takes advantage of homopurine/homopyrimidine oligonucleotides that form triple helices with intact duplex genomic DNA.

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Combinatorial Oligonucleotide (COMBO)-FISH

#10
Front (Question)

combination of comet assay and FISH analysis. It is used to detect genome region-specific DNA damage. successfully used to determine the sensitivity of telomeres to damage.

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Comet-FISH

#11
Front (Question)

makes use of ultrathin cryosections (150 nm thick) of sucrose-embedded cells. The spatial interrelationship of chromosome territories and the genome organization in the cell nucleus has been successfully studied with this technique.

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Cryo-FISH

#12
Front (Question)

In this FISH, a secondary color is observed since the adjacent colors overlap.

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Double Fusion FISH (D-FISH)

#13
Front (Question)

used to determine DNA fragmentation levels in sperms

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DNA Breakage Detection FISH (DBD-FISH)

#14
Front (Question)

BLAST-based FISH simulation program, which can predict the out- come of hybridization experiments

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e-FISH

#15
Front (Question)

a technique in which DNA fibers or chromatin fibers are released from cell nuclei by salt or solvent extraction and stretched on a microscope slide prior to hybridization

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Fiber-FISH

#16
Front (Question)

in situ hybridization is combined with flow cytometry for measurement of the telomeric signals from cells in suspension

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Flow-FISH

#17
Front (Question)

initially used for identification of the 9;22 Philadelphia translocation in peripheral blood and bone marrow cells of CML patients to detect minimal residual disease after bone marrow transplantation

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Fusion-Signal FISH

#18
Front (Question)

the cells are first permeabilized and then extracted with high salt to remove soluble protein

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Halo-FISH

#19
Front (Question)

a method for cell cycle-controlled chromosome analysis in human lymphocytes that allows a precise quantification of induced chromosome damage for human biodosimetry

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Harlequin-FISH

#20
Front (Question)

a combination of standard FISH and indirect or direct immuno- fluorescence. With this technique, the antigens can be visualized within the sample.

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Immuno-FISH

#21
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more useful for the detection of mRNA and genes on the chromosomes

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Locked Nucleic Acids (LNAs)-FISH

#22
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the ability to identify several regions or genes simultaneously using different colors; used to analyze specific chromosomal subregions, like centromeres and sub-centromeres

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Multiplex (M)-FISH

#23
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refers to the simultaneous use of multiple probes in multicolor FISH. This FISH assay was initially designed to screen for multiple microdeletion syndromes in patients with unexplained developmental delay and/or mental retardation.

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Multilocus or ML-FISH

#24
Front (Question)

first used to measure individual telomere lengths on metaphase chromosomes

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Peptide Nucleic ACid (PNA)-FISH