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OGT’s Expanded NGS Cancer Panels Enable Sequencing of Difficult Genes

publication date: May 26, 2017
 | 
author/source: Oxford Gene Technology

New SureSeq myPanel™ NGS Custom Cancer Panel content covers a wider range of cancer types with excellent coverage uniformity for confident results

OGT expanded NGS cancer panels enable sequencing of difficult genesOxford Gene Technology (OGT), The Molecular Genetics Company, has expanded its SureSeq myPanel™ NGS Custom Cancer Panel content. The expansion comes in response to NGS becoming ever more important for research into an increasing number of cancer types, and a need to obtain reliable data for difficult-to-sequence genes and mutations. The expanded content now covers over 70 genes, with many more available in the near future, optimised for haematology and solid tumours including breast, colorectal, lung, ovarian and prostate cancer, glioma, melanoma, sarcoma, leukaemias, myeloproliferative neoplasms and myelodysplastic syndrome.

The strength of OGT’s hybridisation-based bait design coupled with its unique expertise delivers excellent whole gene coverage, unparalleled uniformity and the ability to sequence even the most difficult of regions. This yields reproducible and meaningful data, enabling researchers to be confident in sequencing results and analyses.

Some of the most difficult cancer-associated genes to sequence are those that have high levels of GC-rich content, such as the tumour suppressor gene CEBPA in acute myeloid leukaemia, and TP53, which is frequently mutated in many cancer types including breast cancer. In addition, genes that contain internal tandem duplications are challenging to target due to their repetitive nature and length. Panels available from other suppliers can experience problems with data variability, coverage drop-out or masked mutations in these regions. In contrast, OGT’s innovative bait design uniquely overcomes these issues, delivering the high levels of uniform coverage required, and reducing the need for supplementary fill-in by Sanger sequencing.

This unique design allows researchers to detect low frequency variants consistently down to 1% VAF (variant allele frequency) at a read depth of >1000x. The panels are fully customisable—researchers can select the gene, exonic or intronic content needed to create an NGS cancer panel that meets their exact requirements. All the content is fully pre-optimised, removing the need for lengthy in-house optimisation, reducing assay development time.

Dr Anna Skowronska, R&D Scientist at West Midlands Regional Genetics Laboratory, has been using the SureSeq Myeloid Panel content. She commented: “We’ve found that the SureSeq Panel performs very well and has detected all known positives with an excellent variant detection of around 1%... we were positively surprised right from the very first analysis by the level of mutation detection achievable.”

OGT closely collaborates with leading experts and examines the current literature to provide the most up-to-date targeting of all relevant regions. This includes exonic, intronic and splice sites, and delivers comprehensive insight into disease-driving mutations. Dave Cook, Senior Product Manager at OGT elaborated: “We’re continually working to expand our custom NGS panel content to ensure we have the most recent and relevant content. Our coverage and reproducibility is unrivalled in the market and we wanted to expand the accessibility of quality NGS data to a wider range of cancer types—including genes and regions that are known to be difficult to sequence. We’re committed to helping customers reach their goals and we’re pleased to report that our expertise has enabled us to overcome these sequencing difficulties, giving them more confidence in the data they are generating”.


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