Smart NGS Solutions and Bioinformatics for Research and Health
From tissue to results- full service for all your samples
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.
MACE kit comes to Japan
We are glad to announce that we have signed an agreement for the distribution of our MACE kit in Japan with FUNAKOSHI, one of the leading life science traders in Japan.
GenXPro at the “Innovation Days 2016”
CEO Dr. Peter WInter presenting the Innovative MACE Technology at the Innovation Days 2016 in Bonn.
Drug decision based on gene expression and mutations
GenXPro wins PerMediCon-Award!
We are proud to have received the PerMediCon award 2016 with our Triple-T: Rationalized Tailored Targeted Therapy concept
inhibition in cancers!
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.
Our portfolio comprises:
Precision Medicine, Theranostics, Liquid Biopsy, Illumina, 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, MethylSeq, Exome Sequencing, Target enrichment, qPCR, Bioinformatics, SMART Breeding, TrueQuant, UMI, Molecular Barcodes, Target sequencing of Poly-A tags, PATs, ATAC-Seq, Microbiome, Metagenome
Our services and producs are for research use only.