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.

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 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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Our Services:

Our customers say... 

“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

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