Transcriptomics, Genomics, Epigenomics, Bioinformatics
Nucleotide-based information screening.
By combining intelligent sample preparation with latest next generation- or "deep sequencing" methods, we analyse transcriptomes, genomes and epigenomes at highest resolution.
Our service comprises project planning, consulting, sample preparation, sequencing and bioinformatics.
Meet us in Barcelona at the "Omics meet translational Research" workshop, the 25th and 26th of September!
Thanks to many years of experience with deep sequencing, we have accumulated vast knowledge in low-bias sample preparation of all kinds of different biological samples and provide appropriate solutions for all areas of life science.
Our team of bioinformaticians applies most advanced methods and designs individual solutions to handle the data on our powerful CPU clusters.
Data is delivered in ready-to-use format and includes quality information, quantification, annotation, mapping, Gene Ontology analysis, plots and other graphics.
Our unique “TrueQuant” methodology eliminates PCR-introduced bias. We therefore provide truly reliable quantification of transcripts, copy number variations, or methylation-specific tag-counts- even if it was PCR-amplified from minute amounts.
We would be looking forward to discussing your project with you!
Please click here for our brochure in English or in German language.
Please click here for more information about our service:
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Keywords of our portfolio are:
RNAseq, deep Seqeuncing, 3’ DGE, SuperSAGE, MACE, PARE, Transcriptomics, De novo Sequencing, Assembly, SNPs, Copy Number Variations (CNVs) , RADseq, Reduced Representation Libraries, Normalisation of cDNA and DNA, CpG Islands, Methylation, Digital Karyotyping, Exome Sequening, Target enrichment, qPCR, ChiP Seq and barcoded Sequencing, Bioinformatics.