Cytocell® FISH Probes
High-quality range of FISH probes for the detection of gene rearrangements related to inherited genetic disease and cancer.
SureSeq myPanel™ NGS Custom Cancer Panels
A regularly updated, expert-curated library of pre-optimised cancer panel content for you to select from. Simply mix and match the gene, exonic or intronic content you need to create an NGS cancer panel that meets your exact requirements.
SureSeq™ Ovarian Cancer Panel
A hybridisation-based NGS enrichment panel with complimentary SureSeq Interpret Software that delivers accurate and easy identification of variants.
SureSeq™ Myeloid Panel
A 25-gene myeloid disorders hybridisation-based NGS enrichment panel with complimentary SureSeq Interpret Software that delivers accurate and easy identification of variants.
SureSeq™ Solid Tumour Panel
Fully validated on FFPE samples, the 60-gene NGS SureSeq Solid Tumour Panel allows discovery of novel and known variants in a range of solid tumours.
SureSeq™ FFPE DNA Repair Mix*
Effectively repairs DNA damage, common in FFPE samples, improving library yields, on-target rates and mean target coverage, while removing fixation and storage artefacts, and reducing the amount of starting material required.
SureSeq™ NGS Library Preparation Kit
Streamlined library preparation for industry-leading next generation sequencing (NGS) results.
CytoSure™ Cancer +SNP Arrays
Reliable detection of copy number changes and loss of heterozygosity on a single array for the haematological malignancies and solid cancers
CytoSure™ Custom Designed aCGH Arrays
Focused custom aCGH arrays designed by the microarray experts.
CytoSure™ Genomic DNA Labelling Kits
Efficient and reproducible labelling of DNA samples for use in aCGH.
CytoSure™ Interpret Software
Effortless translation of oligo aCGH data into meaningful results.
High-quality products for processing aCGH samples.