Multiplatform strategies as the means to success
High quality results through optimized project design
Exploit our many years of experience in genome projects - de novo and re-sequencing projects of any size – and achieve top quality results through combining different sample preparation methods, the latest sequencing technologies and adapted bioinformatics tools, e.g.:
De novo sequencing
= Backbone sequencing with Roche GS FLX+ or Illumina HiSeq 2000
+ scaffolding & contig orientation using paired end reads from different sized insert libraries
+ finishing using Sanger sequencing on ABI 3730xl
+ made-to-measure bioinformatics for every budget: From raw data via the assembly right through to the annotation
Re-sequencing
= Illumina HiSeq 2000 | single or paired end reads from different sized insert libraries for the analysis of SNPs, InDels or re-arrangements
+ made-to-measure bioinformatics for every budget: From raw data via the mapping right through to the SNP and InDel analysis
Spotlight
Customer Service
(D) +49 - 7531 81 60 68
(F) +33 - 4 91 82 84 88
(GB) +44 - 207 691 4921
(S) +46 - 8 655 3609
Opening hours:
8 am - 6 pm CET (Mon-Fri)
NEW! Sequencing Service featuring PacBio RS
Next Generation Sequencing Seminar
Next Gen Specialists on site
Genomics & Transcriptomes
Analyses & Visualisation
On the path to a deep understanding of the organism, two parameters are important to the interpretation of the Next Gen sequencing data: The use of various Next Gen systems to take advantage of each technology and the combination of different bioinformatic tools and their stepwise application.
Interested? Like to book us for a seminar? Contact us!
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