Xpress genomics page

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 →

Plate-based full-length scRNA-seq

We provide large-scale service of full-length single-cell RNA-seq to customers worldwide.

Xpress-seq profiles polyA+ RNA with state-of-the-art sensitivity and coverage.

Development of single-cell RNA-seq methods has traditionally focused on increasing cell numbers profiled or improving the transcriptome information. Xpress-seq is the first method to enable high-quality data for large numbers of cells.

Xpress-seq resolves cell types and sub types in complex tissues at unprecendeted resolution.

Thanks to the sensitive capturing of RNAs per cell, low-expressed marker genes are reliably detected in most cells. This significantly improves the identification of cell types and sub types from complex biological samples.

Xpress-seq empowers alternative splicing analyses in single-cells.

Xpress-seq has optimized full-length coverage of short reads along RNA transcripts and thus captures splice junctions. Thus, our users are empowered to analyze alternative splicing at high scale.

Xpress-seq enables allelic RNA profiling in single-cells.

Thanks to Xpress-seq full-length coverage of short reads along the RNA transcripts, transcribed genetic variation can be used to measure allele-resolved gene expression. This is important for studies of cancer, allelic regulation (including genomic imprinting, X-chromosome inactivation, allelic exclusion) and stochastic transcription.

How to Order

Email to order

Receive 384-well lysis plates from Xpress Genomics. To request lysis plates, please email us - we are happy to help you out.

The customer sorts individual cells of interest into the 384-well plates ( → we provide SOP on FACS sorting), stores the plates in -80. When sufficient numbers of plates are ready, the customer returns the plates to Xpress Genomics.

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.

Email us now → to explore all service options and pricing

Xpress Genomics, Stockholm, Sweden. 2024.