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Products
View our integrated portfolio of SureSeq™ NGS panels, Cytocell® FISH probes and CytoSure™ arrays for cancer, constitutional and rare disease research applications.
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 myPanel™ NGS Custom AML Panel
Choose your perfect AML NGS panel from our range of fully tested and optimised panel content. Simply mix and match the genes or individual exons you require and get the most out of your sequencing runs.
SureSeq myPanel™ NGS Custom Breast Cancer Panel
Choose your perfect breast cancer NGS panel from our range of fully tested and optimised panel content. Simply mix and match the genes or individual exons you require and get the most out of your sequencing runs.
SureSeq myPanel™ NGS Custom Colorectal Cancer Panel
Choose your perfect colorectal NGS panel from our range of fully tested and optimised panel content. Simply mix and match the genes or individual exons you require and get the most out of your sequencing runs.
SureSeq myPanel™ NGS Custom Melanoma Cancer Panel
Choose your perfect Melanoma NGS panel from our range of fully tested and optimised panel content. Simply mix and match the genes or individual exons you require and get the most out of your sequencing runs.
SureSeq myPanel™ NGS Custom Prostate Cancer Panel
Choose your ideal prostate cancer NGS panel from our range of fully optimised NGS panel content. Simply mix and match the genes or individual exons you require and get the most out of your sequencing runs.
SureSeq myPanel™ NGS Custom FH Panel
Choose your perfect Familial Hypercholesterolemia (FH) panel from our range of fully tested and optimised content.
SureSeq™ CLL + CNV Panel
The SureSeq CLL + CNV Panel has been designed in collaboration with recognised cancer experts to detect 12 key genes and 5 chromosomal regions implicated in CLL progression.
SureSeq™ Core MPN Panel
The SureSeq Core MPN Panel delivers accurate detection of somatic variants in 3 clinically relevant myeloid-associated genes, JAK2, MPL and CALR.
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™ 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
The complete library preparation solution for unparalleled next generation sequencing (NGS) results.
SureSeq™ Interpret Software
SureSeq Interpret is a powerful and easy-to-use next generation sequencing analysis solution. Optimised for use with SureSeq NGS panels for confident annotation and reporting of low frequency variants.