Whole Genome Sequencing Non-Human

Flexible solutions for non-human samples, including bacteria, animals, plants, yeast, other eukaryotes, or viruses to capture and map all genetic information, encompassing both coding and non-coding regions, and to detect genetic variations and mutations.

Whether using short-read sequencing to identify mutations, or long-read sequencing for de novo assemblies and to detect structural variants or phase mutations, Eurofins provides the optimal tools to support your research needs.

Bacteria Sequencing

INVIEW Resequencing Bacteria

Illumina NovaSeq

INVIEW Resequencing is a streamlined, efficient, and certified NGS service for bacterial genome resequencing, offering high coverage and optional bioinformatics enhancements.

ONT Lite Bacteria Genome Sequencing

ONT GridION

Ultra-fast turnaround long-read sequencing for bacteria with up to 20 Mb genome. Includes high-quality de novo assembly, annotation of all genomic features, and species determination.

Hybrid Assembly Bacteria

ONT GridION & Illumina NovaSeq

Combines 30x long-read data with 300x short-read accuracy to enhances consensus quality at homopolymer regions and methylation motifs, delivering the most precise and reliable bacterial assembly.

Plants, Fungi, Animals

Short-read WGS Non-Human

Illumina NovaSeq

Flexible sequence coverage from 30x to ultra deep including a wide range of input materials inclluding low input DNA.

INVIEW Resequencing Yeast, Fungi

Illumina NovaSeq

For all genomes up to 180 Mb including Yeast and Fungi. The perfect product for a coverage of min 30x.

Long-read WGS Non-Human

ONT GridION

Ultra long-read sequencing with up to 100 kb read length to span large repeat regions and structural variants. Ideal for de novo assemblies.

Features

Services are performed in ISO17025 certified labs in Europe
Latest long-read technologies powered by Oxford Nanopore Technologies
High-quality genome data for de novo assemblies and detection of single nucleotide polymorphisms (SNPs), insertions & deletions (InDels), structural variants (SVs), methylation analysis and copy number variations (CNVs)
Flexible data quantity options.
Wide range of bioinformatics services & interactive analysis reports to provide publication-ready data
Data transfer via secure FTP

High-Throughput Whole Genome Sequencing – Also with MGI DNBSEQ-T7

For large-scale non-human whole genome sequencing (WGS) projects, we also offer sequencing on the MGI DNBSEQ-T7 platform.

This ultra-high-throughput system enables cost-efficient, rapid processing of large sample cohorts — ideal for population studies, breeding programs, biodiversity research, and more.

With its advanced DNB technology and patterned flow cells, the DNBSEQ-T7 delivers high data quality and scalability, making it a powerful alternative to traditional short-read platforms.

Planning a large project?

We’d be happy to discuss your specific requirements and provide a tailored solution. Just get in touch with our NGS experts!

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