Status:
ReviewerMember since: 2015
Organization: Goethe-University Hospital Frankfurt
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!"
Status:
ReviewerMember since: 2015
Organization: Institute of Environmental Biotechnology, Graz University of Technology
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."
Status:
ReviewerMember since: 2015
Organization: Helmholtz
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."
Status:
ReviewerMember since: 2014
Organization: Babylon University
Application Area: Genetic Engineering, Genetic
"It has high frequency and throughput and you are not dependent on a Sanger reaction."
Status:
ReviewerMember since: 2015
Organization: University of Oxford
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. "
Status:
ReviewerMember since: 2015
Organization: DWI Leibniz-Institute f. interactive Materials, Aachen, Germany
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."
Status:
ReviewerMember since: 2015
Organization: IATA-CSIC
"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."
Status:
ReviewerMember since: 2015
Organization: John Innes Centre
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."
Status:
ReviewerMember since: 2015
Organization: University of Tromsø
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."
Advantages of our services:
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.
Manufacturer Eurofins Genomics | Available Worldwide
4.2 / 5.0 | 9 reviews