SERVICES


Single-cell RNA-seq →
Bulk RNA-seq →
Spatial Transcriptomics →
DNA-seq →
Library Sequencing →

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Xpress Genomics
Single-cell RNA-seq →
Bulk RNA-seq →
Spatial Transcriptomics →
DNA-seq →
Library Sequencing →
DNA Sequencing
Flexible services for DNA sequencing
We provide DNA sequencing services that are applicable to many applications and can help facilitate any type of research area.
Versatile
We support a wide range of applications including WGS, WES and amplicon sequencing.
Fast
We offer fast turnaround times and consistent data by leveraging full automation of workflows.
Cost effective
Optimized workflows and cost effective sequencing to enable you to run larger projects with your budget.
DNA-seq service specifications
Input sample type
Genomic DNA, amplicons, plasmids, etc
Library Prep
Enzymatic fragmentation, PCR and PCR-free
Input amount
from 1 ng (PCR-based) or 100 ng (PCR-free)
Multiplexing
Up to 384 samples, higher plex-level on demand
Service
Library construction, sequencing, QC and demultiplexing
Sequencing options
DNBSEQ G99, DNBSEQ G400, DNBSEQ T7 platforms
Read length & depth
SE100, PE100, PE150. Sequencing depth customizable depending on application
Email us now → to explore all service options and pricing
Xpress Genomics, Stockholm, Sweden. 2024.