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Products
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 FH panel
Choose your perfect Familial Hypercholesterolemia (FH) panel from our range of fully tested and optimised content.
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™ 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™ Constitutional v3 and Constitutional v3 +LOH Arrays
Enhanced exon-level CNV coverage of developmental disorder genes and reliable detection of loss of heterozygosity, all on a single array
CytoSure™ Medical Research Exome Array
Comprehensive coverage of medically relevant genes at exon-level resolution.
CytoSure™ Autism Research Array
Exon-focused, high-resolution, 4x180k aCGH array design covering medically-relevant genes for autism research.
CytoSure™ Epilepsy Research Array
Exon-focused, high-resolution, 4x180k aCGH array design covering medically-relevant genes for epilepsy research.