Next Generation Sequencing Service by Eurofins Genomics

Manufacturer Eurofins Genomics  |  Available Worldwide
4.2
/
5.0
  |  9 reviews
High throughput sequencing powered by innovation & expertise. Next generation sequencing is not only deep sequencing but also data analysis and project consulting. Eurofins Genomics is dedicated to defining projects that perfectly fit all your needs by combining state-of-the-art bioinformatics and different NGS technologies.The Eurofins Genomics next generation sequencing service is available on 5 different instruments. To offer you the optimum solution for your application the best technologie... Read more
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Next Generation Sequencing Service by Eurofins Genomics product image
Next Generation Sequencing Service



Average Rating: 4.2
9 Scientists have reviewed this product

5 out of 5
Ease of use
4 out of 5
After sales service
4 out of 5
Value for money


  • Status:

    Reviewer
  • Member since: 2015

  • Organization: Goethe-University Hospital Frankfurt



  • Ease of use
    5 out of 5
    After sales service
    5 out of 5
    Value for money
    5 out of 5
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Rating: 5.0

  • Application Area: if time matters, then I use this product

"This product enable very high Quality results, care is great before, during, AND after sales! You only have to send the samples, so it very easy to use and well, Quality costs!"

Review date: 18 May 2015 | Next Generation Sequencing Service
  • Status:

    Reviewer

  • Member since: 2015

  • Organization: Institute of Environmental Biotechnology, Graz University of Technology



  • Ease of use
    5 out of 5
    After sales service
    3 out of 5
    Value for money
    3 out of 5
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Rating: 3.7

  • Application Area:shotgun metagenomes and marker gene amplicon analysis

"- read counts per sample should be more homogenous - negative controls and blanks could have lower counts of contaminated read fragments - Compatibility of data with standard bioinformatic analysis tools like QIIME could be enhanced - especially due to the barcode design and by providing a barcode read file."

Review date: 07 May 2015 | Next Generation Sequencing Service
  • Status:

    Reviewer

  • Member since: 2015

  • Organization: Helmholtz



  • Ease of use
    4 out of 5
    After sales service
    3 out of 5
    Value for money
    3 out of 5
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Rating: 3.3

  • Application Area:ChIP-Seq library prep and NGS service (1x)

"Service was easy to use. Before sale, extensive contact with sales personnel and tech support. : ) Results fast, but expensive. However, results were of low quality (most likely due to our own fault, not the NGS service), but not follow-up was carried out to troubleshoot."

Review date: 07 May 2015 | Next Generation Sequencing Service
  • Status:

    Reviewer

  • Member since: 2014

  • Organization: Babylon University



  • Ease of use
    5 out of 5
    After sales service
    4 out of 5
    Value for money
    3 out of 5
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Rating: 4.0

  • Application Area: Genetic Engineering, Genetic

"It has high frequency and throughput and you are not dependent on a Sanger reaction."

Review date: 22 Apr 2015 | Next Generation Sequencing Service
  • Status:

    Reviewer

  • Member since: 2015

  • Organization: University of Oxford



  • Ease of use
    3 out of 5
    After sales service
    4 out of 5
    Value for money
    5 out of 5
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Rating: 4.0

  • Application Area:sequencing of plasmids

"Works okay, is easy to use, good value for money. Got an email back from the after sales care person within two hours. "

Review date: 12 Feb 2015 | Next Generation Sequencing Service
  • Status:

    Reviewer

  • Member since: 2015

  • Organization: DWI Leibniz-Institute f. interactive Materials, Aachen, Germany



  • Ease of use
    5 out of 5
    After sales service
    3 out of 5
    Value for money
    5 out of 5
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Rating: 4.3

  • Application Area:I used the service for de novo sequencing a bacterial genome

"NGS library preparation and sequencing service (Roche 454 paired end) as well as sanger sequencing and bioinformatic services were excellent."

Review date: 12 Feb 2015 | Next Generation Sequencing Service
  • Status:

    Reviewer

  • Member since: 2015

  • Organization: IATA-CSIC



  • Ease of use
    5 out of 5
    After sales service
    4 out of 5
    Value for money
    2 out of 5
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Rating: 3.7
"I was very surprised because the high quality of sequencing reads obtained from sequencing project sent to Eurofins Genomics. Additionally, customer support was excellent because technical staff had no problems to accomplish our experimental set up. Communication between both sides was permanent and useful to solve any issue. I have sent two sequencing projects involving DNA amplicon, RNA, and genomic DNA sequencing by MiSeq Illumina technology. I have requested new quotes for additional project and I hope to get better prices in near future. I always recommend your company because the quality of sequencing and customer service despite your prices are little bit higher than competitors. Congrats."

Review date: 12 Feb 2015 | Next Generation Sequencing Service
  • Status:

    Reviewer

  • Member since: 2015

  • Organization: John Innes Centre



  • Ease of use
    5 out of 5
    After sales service
    5 out of 5
    Value for money
    5 out of 5
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Rating: 5.0

  • Application Area:I use the SmartSeq Kit service

"Results are generally fine and reliable. Short sequence runs can be overcome by an increase in plasmid concentration, I have found."

Review date: 11 Feb 2015 | Next Generation Sequencing Service
  • Status:

    Reviewer

  • Member since: 2015

  • Organization: University of Tromsø



  • Ease of use
    5 out of 5
    After sales service
    5 out of 5
    Value for money
    5 out of 5
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Rating: 5.0

  • Application Area:Sequencing of total RNA from kidneys of lupus prone mice

"It was very easy to send the samples and we received very high quality results. The follow up after receiving the results was excellent and we believe that we have got very good value for the money spent. We highly recommend others to use the same service."

Review date: 10 Feb 2015 | Next Generation Sequencing Service
High throughput sequencing powered by innovation & expertise.

Next generation sequencing is not only deep sequencing but also data analysis and project consulting. Eurofins Genomics is dedicated to defining projects that perfectly fit all your needs by combining state-of-the-art bioinformatics and different NGS technologies.

The Eurofins Genomics next generation sequencing service is available on 5 different instruments. To offer you the optimum solution for your application the best technologies are combined individually.

A multitude of well-known and new next generation sequencing (NGS) applications powered by the Illumina HiSeq 2500, Illumina MiSeq and PacBio RSII, Ion Proton and Genome Sequencer FLX+, GS Junior are available. The Eurofins Genomics service is complimented by extremely flexible service times and express delivery which is available upon request.

Our NGS services currently offer:

  • Genome sequencing
  • Transcriptome sequencing
  • Resequencing & amplicons
  • Libraries & bioinformatics

Advantages of our services:

  • Fast turnaround times using latest technology standards
  • More than 5 years of experience in NGS
  • Combined expertise from several partners (e.g. Genomatix, Integrated Genomics)

NGS Favourites
The NGS Favourites are predefined packages which are optimised for specific applications. NGS Favourites were developed and continuously extended based on Eurofins Genomics' expertise from several years in business and thousands of successfully finalised projects.

Product Overview

Next Generation Sequencing Service by Eurofins Genomics product image

Next Generation Sequencing Service

Manufacturer Eurofins Genomics  |  Available Worldwide

4.2 / 5.0 | 9 reviews