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Lexogen’s Data Analysis Solutions

Your analyzed data is just a few clicks away!

  • Based on state-of-the-art Lexogen’s proprietary pipeline

  • User-friendly – no bioinformatic skills required

Lexogen’s Data Analysis Solutions

We offer an automated solution for QuantSeq and CORALL data analysis based on state-of-the-art Lexogen’s proprietary pipeline. Thus, every user, even without bioinformatics experience, can analyze RNA-seq data conveniently and quickly.

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QuantSeq 3′ mRNA-Seq

QuantSeq technology is a simple method focusing on 3’ ends of mRNA molecules to assess gene expression profiles by RNA sequencing easily. For more information, visit QuantSeq Webpage.

Lexogen’s automated solution for data analysis allows researchers to analyze QuantSeq samples conveniently and quickly, even for users without bioinformatics experience. The workflow for our QuantSeq pipeline is shown on the right.

Each QuantSeq FWD and REV kit is provided with codes for free data analysis on Lexogen’s data analysis solution, including differential expression. Data analysis codes for additional runs or bigger files can be purchased from Lexogen. Please get in touch with us at


The CORALL Total RNA-Seq Library Prep Kit enables fast and cost-efficient generation of UMI labelled, stranded libraries for whole transcriptome analyses using Illumina® NGS platforms. For more information, visit CORALL Webpage.

Lexogen’s automated solution for data analysis allows researchers, even those without bioinformatics experience, to analyze CORALL samples in a convenient and fast way. The workflow for our CORALL pipeline is shown on the right.

Data analysis codes for CORALL data analysis are available for purchase. Please contact us at

NOTE! Data Analysis on Lexogen’s data analysis solution is available for a various range of species. Reference genomes for new species can be added upon request. Please note this will incur a fee.

Due to feasibility checks and formatting adjustments, new reference genome implementation timelines are dynamic and, therefore, cannot be precisely guaranteed. We recommend submitting your request as early as possible before sequencing your libraries. New genome upload acceptance is also subject to change in the case of compatibility issues. For all related inquiries, please get in touch with


Frequently Asked Questions

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