Read more about Xpress Genomics services.
Email us to learn more and get a quote.
High throughput sequencing of ready-made libraries
We utilize our extensive experience in NGS and large in-house sequencing capacity to provide sequencing of ready-made libraries at any scale.
Scalable
We support data generation from low output pilots up to the largest projects with an output of billions of reads per day.
Customizable
We are compatible with standard library types and read lengths, but also support custom sequencing primers and setups so our customers can run any type of sequencing project.
Fast
We always strive to deliver the data to you as soon as we can.
Library sequencing service specifications
Input library type
Any type of MGI- or Illumina-compatible library
Library amount
From 60 ng of dsDNA library
Service
Incoming QC, sequencing, and demultiplexing
Sequencing platforms
DNBSEQ G99, DNBSEQ G400, DNBSEQ T7 platforms
Read length
SE100, PE100, PE150. Custom read layouts are supported.
Read depth
80M - 5000M reads per flow cell.
Email us now → to explore all service options and pricing
SERVICES
Xpress Genomics, Stockholm, Sweden. 2024.