MACE-Seq Service

NGS Service

Service for high-sensitive 3'mRNA-sequencing by MACE-Seq for genome-wide gene expression analyses of any poly-adenylated RNA, incl. pat. WO2009152928A2. Suitable for a wide range of tissues and input including single-cell-, FFPE-derived- and other low-input or partly-degraded RNA.

smallRNA-Seq Service

NGS Service

High-sensitive smallRNA-sequencing using the TrueQuant-smallRNA-Seq kit for the analyses of RNA-molecules with a size of 20-80 bps, including miRNA, piRNA, siRNA. snRNA/U-RNA, snoRNA, srRNA, tRF, ysRNA viral or bacterial RNA; pat. nr. WO2009152928A2.

Methyl-Seq Service

NGS Service

Service for comprehensive, genome-wide DNA methylation analysis by Methyl-Seq, optimized for high sensitivity and precision. Ideal for diverse DNA samples, including low-input and partially degraded sources, enabling accurate methylation profiling across a wide range of applications.

TrueQuant MACE-Seq Kit

Kits

TrueQuant MACE-Seq Library Preparation Kit with UMI and UDI for in-house preparation of high-sensitive 3'mRNA-Seq including patented UMI-adapters (WO2009152928A2) for genome wide gene expression analyses of poly-adenylated RNA.

TrueQuant small RNA-Seq Kit (V2)

Kits

TrueQuant small RNA-Seq Library Preparation Kit (V2) including patented UMI-adapters (WO2009152928A2) for high-sensitive smallRNA-Sequencing of any RNA between 20 and 80 bps, suited for EV-derived and single-cell amounts of RNA, detects miRNA, piRNA, siRNA. snRNA/U-RNA, snoRNA, srRNA, tRF, ysRNA viral or bacterial RNA.

Bioinformatics for Exome-Seq

Bioinformatics

Our Exome-Seq bioinformatics service provides comprehensive analysis of coding regions, optimized for high-resolution variant detection, functional annotation, and interpretation. In addition to variant calling, SNP, and indel identification, we offer specialized analyses including Homologous Recombination Deficiency (HRD) assessment, Tumor Mutational Burden (TMB) calculation, and Human Leukocyte Antigen (HLA) typing.

MACE-Seq Service

NGS Service

Service for high-sensitive 3'mRNA-sequencing by MACE-Seq for genome-wide gene expression analyses of any poly-adenylated RNA, incl. pat. WO2009152928A2. Suitable for a wide range of tissues and input including single-cell-, FFPE-derived- and other low-input or partly-degraded RNA.

PanRNA-Seq Service

NGS Service

Simultaneous analyses of smallRNA and mRNA of model organisms.

QC of RNA

NGS Service

Quality control of RNA with LabChipDXII, quantification with Qubit

smallRNA-Seq Service

NGS Service

High-sensitive smallRNA-sequencing using the TrueQuant-smallRNA-Seq kit for the analyses of RNA-molecules with a size of 20-80 bps, including miRNA, piRNA, siRNA. snRNA/U-RNA, snoRNA, srRNA, tRF, ysRNA viral or bacterial RNA; pat. nr. WO2009152928A2.

RNA-Seq Service

NGS Service

Service for high-resolution transcription profiling through full-length RNA sequencing, targeting poly-adenylated or non-ribosomal RNA. Suitable for comprehensive transcriptome analysis across various sample types, providing insights into gene expression dynamics and enabling detailed study of both coding and non-coding RNA.

Ribo-Seq Service

NGS Service

Analyses of formally ribosome-bound mRNA-fragments (ribosome footprinting) for the analyses of the translatome using our high-sensitive TrueQuant smallRNA-Seq protocol / kit based on pat. WO2009152928A2. The service does not incude the isolation of the ribosomal-bound-RNA, the latter must be provided by the customer.

tRNA-Seq Service

NGS Service

Service for high-sensitive analyses of tRNA fragment (tRF) based on our TrueQuant-smallRNA sequencing protocol and kit (pat. Nr. WO2009152928A2), which was adapted for increased performance for tRNA fragment analyses. The results will also include other smallRNAs.

Targeted Metagenomics (16S) Service

NGS Service

Analyses of 16s rRNA-coding regions (V3 and V4) for high-resolution quantification of bacterial communities by NGS.

Amplicon-Seq Service

NGS Service

Sequencing of PCR products by NGS for the quantitative and qualitative determination of the different PCR-products /amplicons. The results are displayed in a table showing the sequence and its abundance.

Exome-Seq Service

NGS Service

Sequencing of the coding regions of genes from the human genome after hybrid capture using the Illumina whole exome sequencing chemistry 2.5.

ATAC-Seq Service

NGS Service

DNA-Seq Service

NGS Service

Aptamer-Seq Service

NGS Service

5'-MACE-Seq Service

NGS Service

CAGE-Seq Service

NGS Service

Sequencing of capped 5' mRNAs.

Degradome-Seq Service

NGS Service

Methyl-Seq Service

NGS Service

Service for comprehensive, genome-wide DNA methylation analysis by Methyl-Seq, optimized for high sensitivity and precision. Ideal for diverse DNA samples, including low-input and partially degraded sources, enabling accurate methylation profiling across a wide range of applications.

CoV-Seq Service

NGS Service

Whole-Genome-Seq Service

NGS Service

Control Human Reference RNA

Kits

This Control Human Reference RNA serves as a positive control for use with the TrueQuant MACE-Seq library preparation kit and other NGS protocols. It is suitable for various RNA-seq applications, including library preparation and sequencing workflows.

DNA Removal Kit for MACE-Seq

Kits

The DNA Removal Supplementary Kit eliminates residual genomic DNA by specifically degrading DNA while preserving the integrity of RNA.

FFPE Enhancer for MACE-Seq

Kits

FFPE Supplementary Kit is designed to adress Formalin-Fixed Paraffin-Embedded (FFPE) or substantial RNA degradated or fragmented samples, improving cDNA synthesis.

Nuclease-free Water

Kits

qPCR for library quantification

Kits

qPCR kit for library quantification prior to pooling for 24 reactions

qPCR Supplement Kit for MACE-Seq

Kits

The qPCR Supplementary Kit is designed to determine the precise cycle number required for the subsequent PCR amplification of the library

qPCR Supplement Kit for small RNA-Seq

Kits

The qPCR Supplementary Kit is designed to determine the precise cycle number required for the subsequent PCR amplification of the library.

supplemental qPCR kit for smallRNA 96x

Kits

qPCR kit for quanntification of smallRNA NGS libraries 96 reactions

TE Buffer

Kits

TrueQuant MACE-Seq Kit

Kits

TrueQuant MACE-Seq Library Preparation Kit with UMI and UDI for in-house preparation of high-sensitive 3'mRNA-Seq including patented UMI-adapters (WO2009152928A2) for genome wide gene expression analyses of poly-adenylated RNA.

TrueQuant smallRNA-Seq v2 Kit 24x

Kits

TrueQuant smallRNA Seq Kit 24 reactions

TrueQuant small RNA-Seq Kit (V2)

Kits

TrueQuant small RNA-Seq Library Preparation Kit (V2) including patented UMI-adapters (WO2009152928A2) for high-sensitive smallRNA-Sequencing of any RNA between 20 and 80 bps, suited for EV-derived and single-cell amounts of RNA, detects miRNA, piRNA, siRNA. snRNA/U-RNA, snoRNA, srRNA, tRF, ysRNA viral or bacterial RNA.

RSE Kit

Kits

Kit for region-specific extraction (RSE, Generation BIotech) for target enrichment prior to sequencing by NGS.

GXP-16s V3V4 rRNA Kit

Kits

Kit for amplfication and sequencing of 16s rRNA-coding regions (V3 and V4) for high-resolution quantification of members of bacterial communities.

TrueQuant DNA Library Preparation Kit

Kits

TQ-I5; Dual Index Adapter with p7+p5 UMI Index

Kits

TQ-I7I5; Dual Index Adapter with p7+p5 UMI Index

Kits

TQ-DNA-Seq-Library-Preparation Kit

Kits

Bioinformatics Report

Bioinformatics

Comprehensive report for the gene expression results including plots, GSEA, ORA e.g about enriched pathways and detailed descriptions.

Bioinformatics for MACE-Seq

Bioinformatics

Our MACE-Seq bioinformatics service provides comprehensive analysis for high-sensitive 3' mRNA sequencing data, enabling precise genome-wide gene expression profiling. From raw data processing to differential expression analysis, we offer customizable options for transcript quantification, gene expression comparison, and pathway enrichment, delivering actionable insights into gene regulation and expression patterns.

Bioinformatics for smallRNA-Seq

Bioinformatics

Our SmallRNA-Seq bioinformatics service supports in-depth exploration of microRNAs, piRNAs, ncRNAs, and other small regulatory RNAs. We offer end-to-end processing, including small RNA identification, quantification, and differential expression analysis, along with pathway enrichment and microRNAs target prediction to provide a complete understanding of small RNA function and impact.

Bioinformatics for Targeted Metagenomics (16S)

Bioinformatics

Our targeted metagenomics bioinformatics service provides in-depth analysis of microbial communities, including OTU and ASV analysis for species annotation and abundance profiling. We deliver statistical insights like Beta-Diversity, along with a comprehensive list of identified strains/species. The service also features interactive microbiome visualizations, such as Krona plots, heatmaps, and other customizable graphics.

Bioinformatics for Exome-Seq

Bioinformatics

Our Exome-Seq bioinformatics service provides comprehensive analysis of coding regions, optimized for high-resolution variant detection, functional annotation, and interpretation. In addition to variant calling, SNP, and indel identification, we offer specialized analyses including Homologous Recombination Deficiency (HRD) assessment, Tumor Mutational Burden (TMB) calculation, and Human Leukocyte Antigen (HLA) typing.

Bioinformatics for DNA-Seq

Bioinformatics

Bioinformatics for RNA-Seq

Bioinformatics

Our RNA-Seq bioinformatics service provides in-depth transcriptional analysis through RNA-Seq, covering genome-wide profiling of splicing variants, Differential Exon Usage (DEU), and fusion events. Our comprehensive pipeline includes variant calling and differential expression analysis at both transcript and gene levels, providing valuable insights into gene regulation and complex expression patterns.

Bioinformatics for Aptamer-Seq

Bioinformatics

Our Aptamer-Seq bioinformatics service provides precise analysis of Aptamer-Seq data, offering raw data processing and frequency counting of unique tags. Our workflow enables accurate quantification of aptamer enrichment and target binding, making it ideal for high-throughput screening applications and biomarker discovery.

Bioinformatics for 5'-MACE-Seq

Bioinformatics

Bioinformatics for Amplicon-Seq

Bioinformatics

Our Amplicon-Seq bioinformatics service for targeted sequencing analysis delivers high-resolution insights into genetic variants within specific genomic regions. It includes raw data processing, variant calling, and comprehensive allele frequency analysis, enabling accurate profiling of mutations and polymorphisms.

Bioinformatics for Shotgun Metagenomics

Bioinformatics

Our bioinformatics service includes species-level annotation, functional profiling, and abundance estimation, providing a detailed view of community composition and metabolic potential. This service also includes interactive data visualizations, such as Krona plots, heatmaps, and pathway maps, for intuitive exploration of complex microbiome data.

Bioinformatics for tRNA-Seq

Bioinformatics

Bioinformatics for ATAC-Seq

Bioinformatics

Bioinformatics for Degradome-Seq

Bioinformatics

Bioinformatics for Methyl-Seq

Bioinformatics

Our Methyl-Seq bioinformatics service offers a comprehensive pipeline for DNA methylation analysis, optimized for high accuracy and resolution. We handle all stages, including bisulfite conversion, alignment, and peak calling, to deliver precise methylation profiling across the genome.

Bioinformatics for Ribo-Seq

Bioinformatics

Bioinformatics for CoV-Seq

Bioinformatics

Bioinformatics for Whole-Genome-Seq

Bioinformatics

Bioinformatics for Genomics

Bioinformatics

Bioinformatics for Transcriptomics

Bioinformatics

Bioinformatics analysis of transcriptomic features like miRNA, piRNA, tRNA and mRNA.

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