Frequently asked questions

  • We offer all sorts of analysis as well as pre-experiment advice and troubleshooting. So, whatever you need, just contact us and explain us what you need.

  • We offer a wide range of analyses. You can find some examples of previous analysis types we performed. RNA-seq and pathway analysis is the most popular, but most other types of analysis can be performed too. Is your analysis not in this list, not problem, contact us and explain what you need.

  • The fastq files generated by the sequencing machine are all we need.

  • Yes, we can give you publication-ready figures. If you have special wishes, just let us know.

  • We don’t have a set price, as it depends on the type of analysis, the number and size of the samples and what exactly you would need. But just contact us, with the details and we’ll provide you with a quote.

  • Turnover time depends on the type and size of the analysis, but in general we aim to provide you with the results within two weeks. However, if your experiment is really urgent (e.g. resubmission of a paper within a specified deadline), let us know and we can discuss what’s the earliest possible.

  • Yes, our RNA-seq analysis includes pathway analysis too.

  • We offer all sorts of data analysis, including RNA-Seq, scRNA-Seq, Metagenomics, epigenetics and more.

  • We are very happy to give you advice. The combination of many years of wet-lab experience with in-depth knowledge of NGS data analysis places us in the best position to help you achieve the best results

  • Most types of analysis can be done on single-end data, but usually paired-end is better. If you want to know what is best for your experiment, we have this videos that explain how paired-end sequencing works and why paired-end sequencing is usually (but not always) better. This could help you to decide what you need for your experiment. Still not sure? Just contact us and we can advise you.

  • Quality control ensures the accuracy of the data generated by NGS, covering aspects like DNA sample integrity, sequencing accuracy, and base calling.

Do you have a question that is not in the list or do you want more information, contact us here: