Bioinformatiker (w/m/d)
Tasks
- Analyze annotate prioritize genomic variants
- Build reproducible analysis workflows with documentation and version control
- Collaborate with clinicians and scientists on case discussions
- Contribute to precision medicine diagnostic methods
- Develop bioinformatics pipelines for long read genomics
- Implement ai assisted variant prioritization and patient stratification
- Integrate multi omics data and clinical phenotype data
- Prepare standardized outputs for human genetics evaluation
- Process long read sequencing data and perform sample qc
- Support publication and grant preparation
Perks/Benefits
- Access to high-performance computing
- Additional pension benefits
- Collaborative interdisciplinary research
- Conference participation
- Corporate discounts
- Health promotion programs
- Opportunities for scientific qualification
- Public sector job security
- Structured onboarding
- Training opportunities
Skills/Tech-stack
ACMG AMP | Apptainer | BAM | BCF | BED | Bash | CNV analysis | CRAM | Docker | Epigenomics | FASTQ | FIBER-seq | Fusion detection | GFF | GTF | Git | HPC | HPO | Haplotype analysis | IGV | JBrowse | Linux | Long read transcriptomics | Long-read | Long-read Sequencing | Methylation analysis | Nextflow | PacBio HiFi | Phasing | Python | R | RNA-seq | Singularity | Snakemake | Splice analysis | Structural Variant | Structural variant analysis | VCF | Variant analysis | Variant calling | Workflow Management
Education
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