Human Whole Genome Sequencing

Human Whole Genome Sequencing (WGS) captures and maps all genetic information, encompassing both coding and non-coding regions, to detect genetic variations and mutations.

Whether using short-read sequencing to identify germline or somatic mutations, long-read sequencing to detect structural variants or phase mutations, or shallow and low-pass sequencing for cost-efficient variant detection, Eurofins provides the optimal tools to support your research need. 

Short-read human WGS

Illumina NovaSeq

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

Low-Pass human WGS

Illumina NovaSeq

Identify genetic variations, achieving up to 99% accuracy in variant detection even at low sequence coverage (ranging from 0.1x to 10x coverage) by utilizing imputation algorithms.

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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 detection of single nucleotide polymorphisms (SNPs), insertions & deletions (InDels), structural variants (SVs), and copy number variations (CNVs)
Flexible data quantity options.
Wide range of bioinformatics services & interactive analysis reports to provide publication-ready data
Cost-effective low-pass sequencing, and imputation services for genome-wide association studies (GWAS).
Data transfer via secure FTP