full-length RNA-seq
We provide large-scale service of bulk polyA+ 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
0.5-10n ng total RNA
RNA captured
PolyA+ RNA
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 10M reads per sample, can be extended at cost for sequencing
Email us now → to explore all service options and pricing
Opening
Opens Sept 2023 for everyone - without waiting times.
SERVICES
Xpress Genomics, Stockholm, Sweden. 2024.