NGS data analysis
Bulk RNA-seq, DNA-seq, WGS, WES, panels, small RNA-seq, single-cell RNA-seq, ChIP-seq, ATAC-seq, bisulfite-seq, and metagenomics.
- FASTQ, BAM, VCF, count matrices
- QC, statistics, visualization
- Publication-ready deliverables
Send us a short description of the required service — such as sequencing type, number of samples, reads per sample, data format, timeline, and desired deliverables — and we will help define the next steps for your project.
The more project context you provide, the faster we can estimate feasibility, timeline, deliverables, and price.
Bulk RNA-seq, DNA-seq, WGS, WES, panels, small RNA-seq, single-cell RNA-seq, ChIP-seq, ATAC-seq, bisulfite-seq, and metagenomics.
Support for translational genomics, rare disease, oncology sequencing, tumour biopsy data, liquid biopsy projects, and variant-oriented workflows.
AI-assisted bioinformatics workflows for research and industrial partners who need automation, knowledge extraction, or scalable reporting.
You can contact SciBerg by email, phone, or using the project form.
SciBerg is located in Mannheim, close to the Heidelberg biomedical research and life-science ecosystem.
Use the form below to describe your project. This static version uses your email application to send the message to SciBerg.
You can also indicate dates and times convenient for an initial phone call or video conference.