Visualisation software
CytoSure visualisation software is an easy to use data viewing tool complimentary with every Syndrome Plus and ChrX array order. This software provides accurate views of copy number changes relative to genomic position.
CytoSure visualisation software is based on the latest build (36 NCBI) of the human genome and incorporates Copy Number Variation, gene, exon and syndrome annotation to ease data interpretation and build confidence.
Data smoothing and data normalisation can be performed rapidly in just one click.
Data obtained using CytoSure Syndrome Plus arrays and visualised using CytoSure visualisation software.
Results of a dye swap experiment using DNA from a Smith Magenis cell line compared to a normal reference. The Smith Magenis can be clearly seen and the breakpoint accurately mapped.
Data obtained using CytoSure ChrX arrays and visualised using CytoSure visualisation software.
Using the Chromosome X (exon specific) array an approximate 1.5Mb deletion has been identified including the STS gene.
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