Single copy FISH
Our online single copy FISH (scFISH) catalog:
A subscription to our MutationForecaster system provides genome browser access to our genome-wide custom probe designs through the cytogenetic Visual Analytics Decision Support Tool. This tool displays the locations of FISH and oligonucleotide products used in microarray design and hybridization enrichment for Next generation sequencing. If you don’t want to subscribe, you may also contact us to inquire about the probe catalog.
Discovery: Epigenetic differences in metaphase chromosomes detected by single copy fluorescence in situ hybridization (scFISH)!
Cytognomix is the exclusive provider of scFISH products to detect differential chromosome accessibility, as described in these recent peer-reviewed articles:
Khan W, Rogan PK*, Knoll JHM*. Localized, Non-random Differences in Chromatin Accessibility between Homologous Metaphase Chromosomes, Molecular Cytogenetics, 7: 70, 2014.
Khan W, Rogan PK*, Knoll JHM*. Reversing chromatin accessibility differences that distinguish homologous mitotic metaphase chromosomes. Molecular Cytogenetics 8: 65, 2015.
DNA Probes previously verified by FISH. Probes available for numerous congenital disorders, leukemia and other cancer abnormalities. Request one of our standard probes…
FISH probes, genomic microarrays and capture reagents for NGS are based on our patented ab initio technology (US Patents 7,734,424, 8,209,129, and 8,407,013).
Our portfolio also includes other US and international patents covering scFISH probes (eg. US Patents 6,828,097, 7,014,997) , and pending patent applications.
- February 27, 2017. CytoGnomix finalizes contract with Government of Canada
- Jan. 28, 2017. New version of F1000Research paper on chemotherapy response in breast cancer
- January 25, 2017. Comment from the Transforming Genetic Medicine Initiative Blog
- Jan. 23, 2017. Automated interpretation of digital pathology images is currently at an embryonic stage of development