List of services

We offer a range of services, many of which are clinically validated. Examples of the services we provide are listed below. For a more detailed description of the services we offer, see our complete list of services (pdf) Pdf, 105 kB..

Please contact us for further information about our services, pricing and how to set up a project.

Next-generation sequencing (NGS)
We offer NGS based profiling ranging from small gene panels to whole genome sequencing. Technologies that we use include:

  • Haloplex (Agilent Technologies) and Twist-based targeted resequencing
  • Multiplex PCR (Accel-Amplicon)-based resequencing
  • FusionPlex (Archer)-based detection of fusion genes
  • Whole exome sequencing (Twist)
  • Whole genome and transcriptome sequencing
  • Long-read sequencing using Oxford Nanopore or PacBio technology
  • MicroRNA sequencing

ARTIC and Midnight panels.

Detection of altered gene expression and fusion genes using Nanostring technology.

Ultrasensitive detection
Detection of specific genetic variants using Bio-Rad droplet digital PCR or superRCA technology.

Single cell analysis
Single-cell genomics and multi-omics (DNA and protein) using the Tapestri Platform from Mission Bio. We offer customized solutions starting from your single-cell suspension including library preparation, sequencing and data analysis.

Tissue processing
In connection to molecular profiling, we provide support with all tissue processing prior to DNA extraction, including sectioning, staining, slide scanning and determination of tumor cell content (for solid tumors).

Bioinformatics and clinical interpretation
We provide assistance with both standard and project-specific bioinformatic analyses. For clinically validated methods, we also provide clinical interpretation of variants.

Method development
We can undertake projects aimed at development of new, improved methods or applications for diagnostics.

Staff working with sequencing instrument

Photo: Mikael Wallerstedt