WGS Non-Human

Whole Genome Sequencing Non-Human

Whole Genome Sequencing (WGS) - 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.

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.

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.

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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..

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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!

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