“We investigate a complex genomic and molecular interaction induced by CRISPR/Cas9 deletion that requires highly efficient and sensitive target enrichment followed by long-read sequencing. The Samplix Service Team was very knowledgeable and experienced in the specifics of our project. We also received very helpful advice on the data analysis.”
- Keyi Geng, Karolinska Institutet, Sweden
“We used Samplix Xdrop™ and Sequencing Services in a project aiming at closing genomic gaps of the herring Y chromosome. We were pleased with the advice we received from Samplix experts regarding experimental design as well as with the speed and quality of the delivered Service.”
- Prof. Leif Andersson, Uppsala University, Sweden
Photographer: Mikael Wallerstedt
“The Service team has been very efficient, and I have been advised during all steps: from the design of the experiment to optimized methods for high-quality and high-molecular weight DNA extraction from plant tissues. I like the updates I got at each step. I could see the progress of the project and discuss with the team any adjustments that were necessary.”
- Alessandro Tondelli, Council for Agricultural Research and Economics, Italy
Samplix provides target enrichment services using the Xdrop platform together with Oxford Nanopore and/or Illumina sequencing. The properties of our Xdrop platform allow to target and enrich very long DNA fragments. We are therefore able to perform unique enrichment and sequencing projects, including:
• Identify Genomic Integrations, e.g. viral • Verify CRISPR edits • Sequence of repetitive elements, e.g. tandem repeats • Gap closing in difficult genomes • Phase Haplotypes • Amplify Whole Genomes with uniform coverage
See all Xdrop applications
Don't hesitate to contact us, using the form below to learn how your project can be helped by our target enrichment and sequencing services
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