NGS Sequencing
We perform next-generation DNA and RNA sequencing for research, diagnostic and biotech/pharma laboratories. The scope covers library preparation, sequencing and bioinformatics analysis. Results are delivered as raw data (FASTQ) and a report.
Sequencing scope
Whole-genome sequencing (WGS)
Full genome sequencing of prokaryotes and eukaryotes, delivered with FASTQ files, assembly and annotation.
Request a quote →16S rRNA / ITS microbiome profiling
Taxonomic identification of bacteria (16S rRNA gene) and fungi (ITS region) from environmental, clinical and industrial samples.
Request a quote →Shotgun metagenomics
Sequencing the entire DNA pool in a sample to determine the taxonomic composition and functional potential of the microbiome.
Request a quote →Targeted panels and amplicons
Sequencing selected genomic regions or gene sets using amplicon panels, delivered with VCF files.
Request a quote →Transcriptome sequencing (RNA-seq)
Gene expression analysis, identification of splice variants and fusion transcripts, delivered with expression tables and a DEG report.
Request a quote →Bioinformatics analysis
Read quality control, mapping to a reference genome or de novo assembly, functional annotation and statistical analysis.
Request a quote →Workflow
Project specification
We define the research goal, sample type, method and coverage depth.
Library preparation
Nucleic acid extraction, quality control (Qubit, TapeStation) and NGS library construction.
Sequencing
Sequencing on the selected platform with read quality control (FastQC).
Results and report
We deliver FASTQ files (and optionally BAM/VCF) together with a bioinformatics report.
Who is it for?
NGS project quote
Send the number of samples, material type and analysis goal. We will reply with a quote and a proposed workflow.