Read more about Xpress Genomics services.
Email us to learn more and get a quote.
RNA-seq services for any research question
We provide several options for large-scale service of bulk RNA-seq to customers worldwide.
Rapid
We offer the fastest turnaround times on the market.
Scalable
Our efficient workflow saves precious consumables so you benefit from cost-effective prices.
Affordable
Xpress Genomics prepares libraries and performs sequencing (at the customer selected depth). The customers obtains all raw sequencing data (fastq files). Experiments on cells form the human or mouse species also obtains quality control information, as well as alignments (BAM files) towards the current assembly, and gene expression quantifications. Upon delivery of sequencing data, each set of returned plates are invoiced accordingly.
RNA-sequencing qualities with excellent gene detection, read statistics and reproducibility.
We prepare RNA-seq libraries from purified RNA or frozen tissue samples. We operate in 96-well plates and can processed several hundreds of RNA-seq libraries per day.
Xpress bulk RNA-sequencing specifications
Input RNA amounts
0.5-10 ng total RNA (low input) or 10 - 1000 ng total RNA
RNA captured
PolyA+ RNA or total RNA (with rRNA depletion)
Coverage
Full-coverage, including splice variants and transcribed genetic variation
Format
96-well plates, fully automated
Scale
Unlimited
Service
Library construction, sequencing, QC, read alignments and gene quantifications
Sequencing options
PE100 or PE150
Sequencing depth
Default 30M reads per sample, can be customized with competitve cost for sequencing
Email us now → to explore all service options and pricing
SERVICES
Xpress Genomics, Stockholm, Sweden. 2024.