NGS Pre-Analytics


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Automate and accelerate: Focus on insights, not library prep

The faster you can prepare high-quality NGS libraries, the faster you can proceed with sequencing your sample and uncovering insights that accelerate your understanding of its underlying biology. But what if you have thousands of samples? Issues such as manual handling errors, irreproducibility and batch-to-batch inconsistency become magnified the more samples you have to process…. Read article →


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RNA-seq Week 2018 – valuable insights and Q&A from the webinar series

Life science research is constantly on the edge of new technology developments. This trend is especially apparent in advanced transcriptomics and gene expression research. In December 2018, we hosted “RNA-seq Week”, where we presented five different webinars addressing the complete gene expression workflow, starting from sample preparation and ending with bioinformatics analysis. It also included… Read article →


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Find every variant that matters – head-to-head comparison of targeted sequencing methods

In precision medicine, only a handful of DNA variants are going to be relevant for a specific disease or a targeted treatment. Identifying these variants can be difficult, depending on the DNA sample, the specific gene or region and the methodology used to detect them. Next-generation sequencing can deliver precise and accurate information on variants… Read article →