Smart NGS Solutions and Bioinformatics for Research and Health
From minute amounts of material to high-resolution data: full service or kits for all your samples
Plan your next NGS project with us here !
MACE kit
cfDNA-Seq Kit
Gel Free smallRNASeq kit
TrueQuant (UMI) Adaptor kits for up to 386 samples
16s-RNA Seq Kit for Microbiomes
N501Y qPCR Test Kit
E484K-specific qPCR Assay
SARS-CoV-2 qPCR Assay
RELY-viral medium
Whole Genome Sequencing (German)
News |
We mourn the loss of our CEO and founder Dr. Peter Winter (Pit)
His vision drove GenXPro and will continue to drive us. Our thoughts are with his wife and our colleague Cornelia and her family.
CORONA / Sars-CoV-2 /Covid-19
GenXPro partner in EU project for colorectal cancer stratification
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. MACE in the May edition of SCIENCEScience 03 May 2018 MACE in the May edition of NEURONMACE-Seq reveals how 3′ UTRs Modify the Localization, Regulatory Potential, Stability, and Plasticity of mRNAs in Neuronal Compartments NEURON; Volume 98, Issue 3, p495–511.e6, 2 May 2018 MACE kit comes to JapanWe 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. 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! |
Drug decision based on gene expression and mutations>> read more about precision medicine at GenXPro NEW Kit:GenXPro launches single tube, gel-free smallRNA kit for as low as 0.01 ng of total RNA input material. New smallRNA Biomarkers for Pulmonary Hypertension found in Blood with our TechniqueTrueQuant smallRNA kitLange CAK, Lehnert P, Boneva SK, Zhang P, Ludwig F, Boeker M, Hoffmeier K, Horres R, Schlunck G, Reinhard T, Böhringer D, Auw-Haedrich C.Increased expression of hypoxia-inducible factor-1 alpha and its impact on transcriptional changes and prognosis in malignant tumours of the ocular adnexa.Eye (Lond). 2018 Jul 31. Tushev G, Glock C, Heumüller M, Biever A, Jovanovic M, Schuman EM.Alternative 3′ UTRs Modify the Localization, Regulatory Potential, Stability, and Plasticity of mRNAs in Neuronal Compartments.Neuron. 2018 May 2;98(3):495-511 Santos C, Almeida NF, Alves ML, Horres R, Krezdorn N, Leitão ST, Thaïs AF, Rotter B, Winter P, Rubiales D & Vaz Patto MC. First genetic linkage map of Lathyrus ciceraHorticulture Researchvolume 5, Article number: 45 (2018) based on RNA sequencing-derived markers: Key tool for genetic mapping of disease resistance Horticulture Researchvolume 5, Article number: 45 (2018) Tosches MA, Yamawaki TM, Naumann RK, Jacobi AA, Tushev G, Laurent G. Evolution of pallium, hippocampus, and cortical cell types revealed by single-cell transcriptomics in reptiles. Science. 2018 May 25;360(6391):881-888. |
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 apply the most advanced methods and designs individual solutions to handle the data on our powerful CPU clusters in order to provide the optimal analysis pipelines for your data.
Data is delivered in a 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, ctDNA, cfDNA, 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, Tag-Seq, TagSeq, TrueQuant, UMI, Molecular Barcodes, Target sequencing of Poly-A tags, PATs, ATAC-Seq, Microbiome, Metagenome; Amplicon-Seq, small RNA sequencing from palsma, serum (blood).
Disclaimer:
Our services and producs are for research use only.
For testimonials please click here.