“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
Get uniform amplification of your low input samples. Start with as low as a single cell and get enough DNA for Whole Genome Sequencing on Long or Short reads platforms.
With Samplix Whole Genome Amplification Services you can:
Want to check our performance? Look up this dedicated site and download the Application Note and the Poster.
Amplifying every template in separate droplets (droplet MDA) provides a highly uniform sequence coverage, while bulk MDA (Standard WGA) preferentially amplifies certain templates.
Don't hesitate in contacting us. Fill the form below and learn more in details how we can help you amplifying your samples.
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“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