Targeted Sequencing

Our targeted sequencing assays harness the power of next-generation sequencing (NGS) to focus on the specific genes that matter most to your research. Whether you're analyzing a handful of genes or hundreds, our custom panels are designed for high accuracy and depth.

These solutions enable reliable detection of:

Single nucleotide variants (SNVs)
Small insertions and deletions (INDELs)
Copy number alterations (CNVs)
Structural variants, including gene fusions and rearrangements

Focused, Cost-Effective Genomic Insights

Targeted sequencing offers a streamlined approach for investigating variants in selected genomic regions or genes of interest. Because it concentrates on a defined subset of the genome, this method delivers fast, efficient results while reducing sequencing costs. It's ideal for exploring gene function within specific biological pathways and provides a practical alternative to whole genome sequencing (WGS), which requires analysis of significantly larger data sets.

By narrowing the scope of sequencing, researchers benefit from deeper coverage and better resolution in areas of interest—without the added complexity and expense of WGS.

Tailored Panels for Cancer & Beyond

Eurofins offers one of the industry’s most comprehensive cancer gene panel, alongside fully customizable targeted resequencing solutions. Our panels can be adapted to include any genes relevant to your study, whether you're researching cancer-specific mutations or broader genetic questions. We are proud to have been the first to introduce our INVIEW Oncoprofiling panel for circulating cell-free DNA (cfDNA) enabling non-invasive cancer profiling.

Product selection

INVIEW Oncoprofiling 728

Illumina NovaSeq

Our most comprehensive cancer profiling solution, covering all exons of 728 well-characterized tumor suppressor genes and oncogenes, as well as miRNAs and additional key cancer-related regions.

Custom Target Sequencing

Illumina NovaSeq

Benefit from our extensive experience in designing customized enrichment panels.

Whole Exome Sequencing

Illumina NovaSeq

Human exome sequencing at a fraction of the cost of WGS.

Features

• Services are performed in ISO17025 certified labs in Europe
• Fast turn-around times
• Flexible data quantity options
• Optional DNA extraction services available
• Wide range of bioinformatics services & interactive analysis reports to provide publication-ready data
• Data transfer via secure FTP

Wide Range of applications & services

Explore our comprehensive bioinformatics services designed to meet diverse research needs. Our offerings include data analysis, interpretation, and visualization tailored to your specific projects. Benefit from interactive analysis reports that provide clear insights, enabling you to make informed decisions quickly. Our expert team is here to support you every step of the way. Elevate your research with our cutting-edge bioinformatics solutions today!

Quality is important for us at Eurofins

Our products and services are produced and performed under strict quality management and quality assurance systems.

Find Certificates here