CTA Icon

Coming soon! CytoCell IVDR-certified FISH probes. Be the first to know when they are available...

CytoCell Logo

Choose from over one hundred high-quality DNA FISH probes for the detection of genetic aberrations found in cancer and inherited genetic diseases.

Discover more
CytoSure Logo

Featuring the new constitutional NGS platform for cytogenetic research, alongside a broad range of arrays for rare disease and cancer research.

Discover more
SureSeq Logo

Choose from preloaded NGS panels for haematological and solid tumour cancer research or we can help you create your own.

Discover more

Try our handy FISH and NGS product tools

FISH chromosome search

View

Constitutional NGS chromosome search

View

Custom NGS cancer panel builder

View

Featured products

Detect 49 key genes implicated in myeloid disorders

SureSeq Myeloid Plus Workflow

The panel accurately detects SNVs and indels in genes such as CEBPA, JAK2, CALR and MPL, as well as structural variants including FLT3-ITDs and KMT2A-PTDs, and is able to detect low-frequency SNVs and indels with confidence. The figure (right) shows a PTD detection spanning exons 2-8 of the KMT2A gene.

SureSeq Myeloid Plus Workflow Image
CytoSure Comprehensive FH Panel Image

The optimal solution for your FH research

CytoSure Comprehensive FH Panel

Familial Hypercholesterolaemia (FH) is a genetic condition which results in a high cholesterol level and subsequently leads to a higher risk of early heart disease. OGT is offering an optimised NGS panel which has selected the most relevant genes and SNPs implicated in FH, for your research needs. The figure (left) shows a double deletion on the LDLR gene, as visualised by Interpret software.

CytoCell FISH probes for AML and MDS analysis

New...Del(5q) Plus Tri-Colour Deletion & CBFB Breakapart Probes

The triple colour design of the Del(5q) Plus Tri-Colour Deletion Probe facilitates the detection of 5q interstitial proximal and distal deletions, in addition to monosomy 5 in AML and MDS analysis. The CytoCell CBFB Breakapart Probe, with its dual colour, dual fusion probe design, detects rearrangements in the 16q22 region and overcomes limitations associated with the proximity of signals on chromosome 16 during interphase FISH for AML detection.

New...Del(5q) Plus Tri-Colour Deletion & CBFB Breakapart Probes Image

Featured resources & support

View more resources

What binds us, makes us.

We believe that collaboration is key to improving patient lives. By sharing our knowledge and expertise, we ensure that we move forward with our customers, bound by a collective commitment to unlocking the future of genetic clinical care. See our story.

See our story of partnership (130 seconds) Image
Play Icon

See our story of partnership (130 seconds)

Latest OGT news

View all OGT News
OGT launches SureSeq Myeloid Plus panel and Universal NGS Complete Workflow Image

OGT launches SureSeq Myeloid Plus panel and Universal NGS Complete Workflow

05 Oct 2022

Enhanced NGS portfolio includes Interpret Software updates and enables rapid and confident variant detection even in difficult-to-sequence regions.

Read
OGT significantly expands global reach Image

OGT significantly expands global reach

12 Jul 2022

Expansion of access to clinical support network and market-leading genomic solutions aims to improve patient outcomes.

Read
OGT welcomes Adrian Smith as CEO Image

OGT welcomes Adrian Smith as CEO

04 Apr 2022

New leadership will drive OGT’s mission to improve clinical care by partnering with customers.

Read
CTA Icon

Stay up-to-date with the latest news from OGT, including new products, support resources, and our DNA Dispatch newsletter