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> Transcriptome

> RNA-Seq > MACE > Small RNA-Seq/miRNA> Metatranscriptome

> Genome

> Exome Seq > Whole Genome Seq > Target Enrichment

> Epigenome

> Methyl-Seq > Bisulfide-Seq

> Metagenome

> Shotgun-Metagenomics

> Amplicons and Aptamers

qPCR

> Gene Expression Levels

> smallRNA/miRNA

> Copy number variations

> Plasmid number quantification

> Methylation specific qPCR

> Microbe quantification, e.g. 16s RNA

Applications

> Medicine/Pharma

> Agro Sciences

> Non-models

MACEMACE kitTrueQuantBioinformatics> Login

> Omiras

> APADB

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Smart NGS Solutions and Bioinformatics for Research and Health

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News

GenXPro: 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.

>> read more

MACE in Blood

Using the high-resolution MACE Technique, gene expression profiles of newly identified subpopulations of monocytes show distinct expression patterns of SLAN+ cells.

>> read more

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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, applieing 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 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 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:

RNAseq, deep Sequencing, 3Seq, 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

Disclaimer:

Our services and producs are for research use only.

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