Further Information:
>> EVOcard
>> Product FAQs
>> SALE %
Benefit from more than 25 years of experience in oligonucleotide synthesis!
Optimise your research and save time with high quality gene synthesis and molecular biology services.
Hiqh quality Sanger sequencing with highest flexibility for every sample type.
NGS from experts - ISO-certified, fully automated and easy to order online.
Cell line authentication, Mycoplasmacheck, Fragment length analysis & tailored projects.
>> Quality
>> Events
Our genomics solutions support you along your drug development chain of small and large molecules and in precision medicine.
Benefit from our range of tailored, high throughput genotyping solutions to help you achieve your goals faster, for less.
Welcome to your full-service laboratory. Benefit from our end-to end solutions for sample collection kit logistics and genomic solutions.
DNA-based solutions to improve and support your analysis, monitoring and traceability across your value chain.
Our scalable and high-quality oligonucleotides synthesis offer makes us an ideal partner for your industry applications.
For your research project in academic, governmental and industrial environment we have the right genomic service.
Eurofins GenomicsGermany GmbHAnzinger Str. 7a85560 EbersbergGermany
You need support or advice with your order? You don't find the perfect product or you like to get consultation regarding your results?
Please login with your email address and password!
Register a new account at Eurofins Genomics!
Administration
Julian Schlossmacher
Login / Register
Dr. Melvin Siliakus
0 Item(s)
Go to Cart
What are industrial-grade products? <<click here >>
Oligonucleotide Synthesis
Gene Synthesis & Molecular Biology
Next Generation Sequencing
Genotyping & Genexpression
Primers & Probes for qPCR Applications
Oligos for Next Generation Sequencing
Primers for Sanger Sequencing
Oligos for Cloning Applications
Custom Oligos
Oligo Tools
Synthetic genes
GeneStrands
Molecular Biology Services
Sanger Sequencing Services
Prepaid Products for Sanger Sequencing
Additional Services
Genome Sequencing
Transcriptome Sequencing
Metagenome / Microbiome
Exome Sequencing & Oncology Solutions
CRISPR & Prepaid NGS Coupons
VIRUS
Plasmid Sequencing
Amplicon sequencing & Ready-to-Load
Oxford Nanopore projects (WGS, Amplicons, 16S)
ONT Lite
Mycoplasmacheck
CLA & FLA
Others
Order / Refill EVOcard
Long Read Human Whole Genome Sequencing
Human Whole Genome Sequencing (WGS) with long-read technology captures DNA in long, continuous stretches, enabling the detection of structural variants, highly repetitive regions, and complex rearrangements that cannot be resolved by short-read sequencing. This approach provides more complete genome assemblies, revealing large insertions, deletions, and other structural variations. Additionally, it enhances haplotype phasing, aiding in the distinction between maternal and paternal alleles and allows simultaneous methylation analysis for epigenetic studies.
>> Get Quote
>> Order Barcodes
Applications & Services
Additionally, we provide optional services such as structural variant analysis, copy number variation, short tandem repeat (STR) expansion genotyping, and 5-methylcytosine (5mC), and 5-hydroxymethylcytosine (5hmC) detection .
Specifications
>> FAQ's wGS
>> Sample Submission
More details
Important
Please note that only S1-classified material is accepted for DNA isolation ordered online. More information about current classification of biological material can be found here. Please contact us for further information on DNA isolation from material classified as S2.
Solutions you may also like
INVIEW Transcriptome
Analyse the expression levels or splice variants
>> READ MORE
INVIEW Resequencing
Variant analysis for all genomes up to 180 Mb
Eurofins Genome-SeqPortfolio
Get a comprehensive overview
EVOCard
The prepaid card for more flexibility in your research
Quality is important for us at Eurofins
Our products and services are produced and performed under strict quality management and quality assurance systems.