Abstract

The simultaneous and unequivocal discernment of all human chromosomes in different colors would be of significant clinical and biologic importance. Whole-genome scanning by spectral karyotyping allowed instantaneous visualization of defined emission spectra for each human chromosome after fluorescence in situ hybridization. By means of computer separation (classification) of spectra, spectrally overlapping chromosome-specific DNA probes could be resolved, and all human chromosomes were simultaneously identified.

Keywords

KaryotypeChromosomeFluorescence in situ hybridizationCentromereHuman genomeBiologyGeneticsHybridization probeCytogeneticsGenomeComputational biologyMolecular biologyDNAGene

Affiliated Institutions

Related Publications

Parameters of the human genome.

Chromosome arm lengths are the critical parameters of the human genome. The physical length is required to scale radiation hybrid and other maps to megabases. The genetic length...

1991 Proceedings of the National Academy o... 519 citations

Publication Info

Year
1996
Type
article
Volume
273
Issue
5274
Pages
494-497
Citations
1749
Access
Closed

External Links

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

1749
OpenAlex

Cite This

Evelin Schröck, Stanislas du Manoir, Timothy Veldman et al. (1996). Multicolor Spectral Karyotyping of Human Chromosomes. Science , 273 (5274) , 494-497. https://doi.org/10.1126/science.273.5274.494

Identifiers

DOI
10.1126/science.273.5274.494