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