Genome Sequencing - Services By Experts

Whole Genome Sequencing

Whole genome sequencing (WGS) analyzes the complete DNA sequence of an organism's genome, offering detailed insights into its genetic makeup including single-nucleotide polymorphisms (SNPs), insertions and deletions (InDels), copy number variations (CNVs) and structural variations (SVs). At Eurofins, we provide a wide range of cutting-edge long- and short-read sequencing technologies to meet diverse research needs, such as generation of single contiq assemblies.

short-read WGS

Illumina NovaSeq, MGI DNBSEQ-T7

State-of-the-art genomic packages for all genomes using short- and long-read technologies.

long-read WGS

ONT GridION & PromethION

Find perfect flexible solutions for all samples, including bacteria, animals, plants, human, yeast, other eukaryotes, or viruses.

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Features

Services are performed in ISO17025 certified labs in Europe
Fast turn-around times
Flexible data quantity options
Optional DNA extraction services available
Flexible data quantity options
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!