You’re asking complex genomics questions. We use Xdrop® to answer them. Partner with the Samplix® Service Team and enrich genome regions longer than 100 kb.

“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

colabs Keyi Geng

“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

colabs Leif Andersson pgotographer Mikael Wallerstedt

Photographer: Mikael Wallerstedt

Samplix Services Overview

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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