WE217831-sho-benefits-targeted-NGS-tech

Get more from your tumor sample with next-generation sequencing

With next-generation sequencing (NGS) you can get more results, more quickly in a single test. Traditional genetic testing methods involve the use of single gene tests performed in succession to determine the presence or absence of variants of interest. Because of the sample size requirements for running each of these tests and the number of tests required to narrow in on the right answer, sequential testing can often lead to inconclusive results. Additionally, sequential testing can be laborious and expensive, requiring many days or weeks of work before finding the right answer.

或者，通过 NGS，您可在单次实验中使用单一样本，同时搜索目标变体。您可通过单次运行获取 SNP、indel、CNV、基因融合和表达结果。使用 Ion PGM 系统和 Ion AmpliSeq 技术，您只需 10 ng 样本即可获得这些结果。

了解有关 Ion AmpliSeq 技术的更多信息

使用 NGS 的癌症研究人员已贡献了大量遗传信息，这有助于在功能性水平上阐明许多癌症基因中突变的影响。

Dr.Cree

"通过 Ion AmpliSeq 结肠&肺癌检测组合的 Ion PGM 系统上的基因检测组合测序，我们可以一次检测数十个基因的变化，而不仅仅是您碰巧在少数热点区查找的特定突变。"

Ian Cree，医学博士、博士
病理学教授
华威大学
英国
OncoNetwork Consortia

仅供科研使用，不可用于诊断目的。