Don’t forget…Our FAS team can be contacted online with free support advice
OGT’s Chromosome search tool explores hundreds of genes included in the CytoSure® Constitutional NGS panel, their chromosomal locations, common alterations in these genes, and resulting phenotypic characteristics.
Measurable residual disease (MRD) detection via NGS has become an essential tool in myeloid malignancies research. This scientific poster discusses how OGT’s Universal NGS Workflow library preparation demonstrates capabilities suitable for MRD detection, with a VAF down to 0.02%.
Take your research to the gold standard. Interested in learning how SNP arrays are being used in cancer research? View our recent seminar at the Cancer Genomics Consortium (CGC) 2022.
Reduce your NGS library preparation with OGT's Universal NGS Complete Workflow Solution. Our library preparation provides a fast, accurate, and cost-effective workflow.
When it comes to NGS, your results are only as good as your starting material. Discover our six top tips to help you improve your sequencing library. Discover our six top tips to help you improve your sequencing library.