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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.
WGS - Human
Illumina NovaSeq, MGI DNBSEQ-T7
State-of-the-art genomic packages for human genomes using short- and long-read technologies.
WGS - Non-Human
Illumina NovaSeq, MGI DNBSEQ-T7 or ONT GridION
Find perfect flexible solutions for non-human samples, including bacteria, animals, plants, yeast, other eukaryotes, or viruses.
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Features
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!
Literature
Press Release: Eurofins’ Scientists Discover Genetic Differences Between “Identical” Twins
Press Release: Genome Sequencing Analysis Of Ash
DNA Universe Blog
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Resequencing
For all genomes up to 180 Mb
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WGS using Illumina
Whole genome sequencing (Human / Mammal)
WGS using GridION
Long read technology for WGS
RNA-Seq
Transcriptome sequencing of Pro- or Eukaryotes
Quality is important for us at Eurofins
Our products and services are produced and performed under strict quality management and quality assurance systems.