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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.
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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
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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
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Whole Genome Sequencing Select - Long Read
Whole Genome Sequencing (WGS) with long-read technology captures DNA in long, continuous stretches, enabling de novo assemblies, the detection of structural variants, highly repetitive regions, and complex rearrangements missed 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.
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Application & Services
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Library preparation (amplification-free) including fragmentation to ~20kb fragment length ; using v14 library prep chemistry
Sequencing using Oxford Nanopore PromethION or GridION (flow cell R10.4.1)
Whole flow cells dedicated to your samples
Approx. 50 - 100 Gb per PromethION or 6-7 Gb per GridION flow cell (dependent on DNA quality and length)
Number of samples per flow cell depends on genome size and scientific question:
Theoretical coverage achieved based on genome size and sample number multiplexed per flow cell
*Expected output of approx. 7GB / GridION flow cell and approx. 90GB / PromethION flow cell and even read distribution between samples. Long read coverage is calculated as (giga bases (Gb) per flow cell) ÷ (genome size)
Depending on the goals of your studies, we recommend the following coverage for whole genome sequencing:
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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.