Use different dyes after fixing chromosomes in aldehyde or osmium tetraoxide. Make the chromosomes color with improved staining techniques, including R-, T-, C-, and G-staining.Comparative genomic hybridization (CGH) [19] and spectral karyotyping (SKY), which are based on the FISH technique, are relatively recent and improved techniques of chromosomal analysis. The most common methods of dyebased chromosome banding are G-(Giemsa), R-(reverse), C-(centromere) and Q-(quinacrine) banding. Bands that show strong staining are referred to as positive bands; weakly staining bands are negative bands. However the staining patterns are not black and white, different bands stain to different intensities (Francke, 1994). G-positive bands are usually just called G-bands and likewise for Rpositive (R-) bands. Positive C-bands contain constitutive heterochromatin. Q-bands are considered equivalent to Gbands. The most widely used function-based banding method is replication banding and is based on the fact that different bands replicate their DNA at different times during S phase of the cell cycle. Generally, R-band DNA is replicated earlier than G-bands (Dutrillaux et al., 1976). G-bands also correspond to the condensed chromomeres of meiotic chromosomes and R-bands to the interchromomeric regions.