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Next Generation Sequencing

RNAseq Solutions

End- to end NGS solutions with superior performance & simple workflows

NUGEN RNA-Seq: Modular solutions for any application and any organism

  • Whole transcriptome, expression profiling, viral detection and single cell studies (with UMis)
  • Complete RNAseq solutions also for model organisms (e.g. Arabidopsis, Drosophila)
  • Special: Targeted, customizable depletion of transcripts such as ribosomal RNA and other unwanted/uninformative transcripts:
  • Your benefit: increased dynamic range, reduced sequencing costs, and simplified data analysis
  • More data with less sequencing!

Lexogen – Technologies for transcriptome analysis

Methyl-seq Epigenetics

Swift Biosciences’ Methyl-Seq Products

Swift Biosciences offers solutions for whole genome bisulfite sequencing as well as targeted bisulfite sequencing applications, such as RRBS and hybridization capture.

Accel-NGS Methyl-Seq DNA Library Kit: The gold standard for single-base resolution of methylomes. Accel-NGS Adaptase Module: Prepare Single-Cell Methyl-Seq Libraries.

NuGEN’s Methyl-Seq product line

is comprised of library preparation and bisulfite conversion tools for a broad range of applications for NGS, methylation arrays, and more. Now, with the integration of TrueMethyl® oxBS chemistry, gain new insight into epigenetic modifications with the ability to interrogate both 5mC and 5hmC. Products: Ovation® Ultralow Methyl-Seq library system and The Ovation® RRBS Methyl-Seq system

DNAseq library preparation and panels

Swift Biosciences

Innovative NGS library prep solutions for whole genome, exome, targeted sequencing and epigenetic analysis. Compatible with degraded and limited samples with easy and fast workflows of appr. 2h. Applicable across the three major NGS platforms: Illumina, Ion Torrent, and Pacific Biosciences.

DNA sequencing library kits for use with double-stranded DNA, single-stranded DNA, and bisulfite-converted DNA.

Targeted Panels from Paragon Genomics and Swift Biosciences

CleanPlex® NGS panels are powered by Paragon Genomics’ CleanPlex Technology, which uses a proprietary multiplex PCR background cleaning chemistry to effectively remove non-specific PCR products, resulting in optimized, best-in-class target enrichment performance and efficient use of sequencing reads.

Low-input, fast 2-3h workflow and high performance NGS panels to target up to >20,000 amplicons in a single tube reaction. Available as catalog products and cost-efficient custom solutions. Especially suitable for clinical and translational research:

  • Tumor Mutation Burden (TMB) Profiling
  • Early Cancer Detection via Liquid Biopsies (with Molecular barcoding UMI)
  • Mitochondrial Disease Testing
  • Infectious Disease Research
  • Agrigenomics High-Throughput Genotyping




  • Accel-Amplicon® Plus Colorectal (CRC) Cancer Panel
  • Accel-Amplicon® Plus Lynch Syndrome Panel
  • Accel-Amplicon® Plus Lung Cancer Panel
  • Accel-Amplicon® Plus Myeloid Panel


  • Accel-Amplicon® Plus 57G Pan-Cancer Profiling Panel
  • Accel-Amplicon® Plus Comprehensive TP53 Panel
  • Accel-Amplicon® Plus BRCA1 And BRCA2 Panel
  • Accel-Amplicon® Plus BRCA1, BRCA2, and PALB2 Panel
  • Accel-Amplicon® Plus EGFR Pathway Panel
  • Accel-Amplicon® Plus CFTR Panel
  • NEW: Swift Amplicon™ 16S + ITS Panel

NUGEN DNA-Seq – Quantitation-free, titration-free, dimer-free

  • Whole genome and targeted library construction for fresh/frozen, liquid biopsy, FFPE and ChIP samples
  • Simple, streamlined workflows that save time and improve consistency
  • DimerFree technology: no sequencing reads wasted to adaptor dimers
  • New Celero DNA-Seq: fast, addition only workflow with no inline bead purifications
  • NuQuant: novel library normalization method that eliminates qPCR and bioanalyzer for library pooling (included in Celero DNA-Seq)

Check also Allegro: A Cost-effective Solution for Targeted Genotyping with sequencing. Low cost per data point!


Lucigen DNAseq solutions

NxSeq® AmpFREE Low DNA Library Kit and Single Index Adaptors – No Amplification Bias

  • Higher percentage of DNA fragments are sequenceable
  • More uniform sequencing coverage of each sample
  • More complex libraries and better sequencing data
  • Fast and efficient protocol, DNA libraries in ~2 hours
  • Minimal Input (75 ng sheared DNA)


NxSeq® UltraLow DNA Library Kits – Single and Dual Indexing Kits
High Quality Data: Produces more complex libraries with more uniform
sequencing depth and better coverage due to high efficiency adaptor ligation

  • Sensitive: Works with as little as 50 pg to as much 75 ng of fragmented DNA input
  • Minimal Bias: Robust, uniform PCR amplification improves coverage uniformity
  • Fast: 3 hour protocol gets samples on the sequencer faster (Single tube libraries)
  • High Value: Cost-effective library and indexing kits without sacrificing sequencing
  • For high-troughput: NxSeq® UltraLow DNA Library Kit, 96 Reactions and NxSeq® HT Dual Indexing Kit – Optimized for 96-well Plates
  • Easy-to-use & Clear Protocol: Two color dual indexing primer sets facilitate visual verification of correct primer dispensing

Metabion oligos

High quality, cost-efficient & customizable oligos for all applications including PCR, qPCR and NGS. In tubes or in 96-format. Ask for a Metabion option!

Genevia Technologies

Genevia Technologies is a privately held Finnish bioinformatics company established in 2011. Genevia provides bioinformatics research services from planning to completion, usually a publication or a custom-made data analysis pipeline.