10 years GenXPro:

Smart NGS Solutions and Bioinformatics for Research and Health



MACE – the Kit!

GenXPRo has forged its 10 years of experience in NGS library production in its MACE kit for 3′ End Sequencing!

The MACE kit is available in a 6x version (miSeq) and a 24x (HiSeq) version and can be combined to analyse 96 or more samples simultaneously.

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The Virtual Tumor Board

Our unique tool for precision medicine is available. Our tool identifies the druggable pathways and targets in a tumor. Please inquire for further information.


>> read more about precision medicine at GenXPro

Meet us at the Analytica in Munich!

10-13 Mai 2016

Messe München

Halle A3| Stand 320

Experts for sample preparation, sequencing and bioinformatics:

Transcriptomics, Genomics, Epigenomics, Metagenomics

By combining intelligent sample preparation with latest next generation sequencing methods, we analyse transcriptomes, genomes and epigenomes at highest resolution.

Our service comprises project planning, consulting, sample preparation, sequencing and bioinformatics.

In 2008 we invented “TrueQuant” – applying unique molecule identifiers for PCR bias reduction of NGS data.

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 data analyses solutions for all areas of life sciences.

Our team of bioinformaticians applies most advanced methods and designs individual solutions to handle the data on our powerful CPU clusters and provides the optimal analysis pipelines for your data.

Data is delivered in ready-to-use format and includes quality information, quantification, annotation, mapping, Gene Ontology analysis, plots and other graphics.

Keywords of our portfolio are:

Precision Medicine, Theranostics, RNAseq, deep Sequencing, massively
parallel sequencing, 3’Seq, exosomes, small RNA, miRNA, micro RNA, SuperSAGE, MACE, Massive Analysis of cDNA Ends, PARE, Transcriptomics, De novo Sequencing, Assembly, SNPs, Copy Number Variations (CNVs) , RC-Seq (a variant of RADseq), Genotyping by Sequencing, GBS,  Normalisation of cDNA and DNA, CpG Islands, Methylation, MehtylSeq, Exome Sequencing, Target enrichment, qPCR,  Bioinformatics, SMART Breeding, TrueQuant, UMI, Molecular Barcodes, Target sequencing of Poly-A tags, PATs


Our services and producs are for research use only.