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Next generation sequencing services: fast turnaround times using latest technology standards – such as the PacBio RS system, the Illumina HiSeq 2000 system and the Roche GS FLX system, operated with Titanium reagents.

PacBio RS – third generation Single Molecule Real Time (SMRT) sequencing

By including the Single Molecule Real Time (SMRT) DNA sequencing technology from Pacific Biosciences in our portfolio, you have now access to the latest NGS technology on the market.

Current average read length is more than 1000 bp, with more than 10% of reads in a range of 1500 bp to 2500 bp. Some reads are already longer than 4500 bp. With the recent technical updates, the sequencer delivers approximately 35 Mbp of sequencing data per SMRT cell.

Because of the long read length, the SMRT technology is particular well-suited to de novo sequencing of viruses, bacteria, and fungi. SMRT technology also offers advantages for resequencing and scaffolding projects.

HiSeq 2000 – cost efficient Illumina Sequencing

Illumina HiSeq 2000 delivers up to 250 Gb per sequencing run with the 2x100 bp module. This makes HiSeq 2000 the ideal solution for resequencing of genomes or exomes where reference sequences are available.

We offer a broad HiSeq 2000 portfolio that guarantees cost-efficient sequencing data for your applications.

Genome sequencing >
Targeted resequencing of sequence capture experiments >
Illumina mRNA sequencing
Illumina ChIP sequencing
Illumina small RNA sequencing
Bioinformatics services >
Library generation services >

Roche Genome Sequencer – GS Sequencing by the Experts

Roche GS FLX sequencing is the technology of choice for de novo sequencing of genomes of any size. The long read length, together with our well-established expertise in long paired-end (LPE) libraries from 3 kb to 40 kb, guarantees the best possible quality of assembly data. With the addition of the GS Junior to our sequencer fleet, we also offer small scale projects with even faster turnaround times.

Genome sequencing >
Transcriptome sequencing >
Resequencing of exons and genome fragments >
Small RNA sequencing
Amplicon sequencing >
Ultra deep sequencing of exons and genome fragments >
Bioinformatics Services >
Library generation services >

Next Generation Sequencing – Tailored Solutions for your Projects

Depending on your final objective, we will assist you in designing the appropriate sequencing experiment for your research. In close consultation with you, we will work out the strategy to deliver the best possible data quality.

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