REEF: disease-level signature explorer
With Dr. Burak Demircan, Hematology and Oncology, University Hospital Frankfurt
Pools cell lines belonging to one disease and extracts the signature they share:
commonly and selectively essential genes from CRISPR screens, plus consensus up- and
down-regulated genes from expression data. Scoring combines effect size with
cross-line consistency, so single-line outliers do not dominate.
Manuscript in preparation.
- R
- Shiny
- CRISPR screens
- DepMap-style data
Open the app
hosted on a free tier, allow a moment to wake
TurboID interactome pipeline
RWTH Aachen, Institute of Molecular Immunology and Biochemistry
Analysis pipeline for TurboID and BioID proximity-labeling proteomics: contaminant
handling, enrichment against the appropriate labeling control, statistical testing and
interpretation of proximal interactors.
Underlies the IRE1 interactome published in Cells (2024).
- R
- Proteomics
- Mass spectrometry
Repository
Paper
Base editing screen with single-cell readout
University Hospital Frankfurt, Department of Hematology
Built a CROP-seq system for cytosine and adenine deaminase base editors, from vector
design and viral transduction through to editing validation, so that guide identity and
transcriptome can be read out from the same cell.
Screening system established and handed over; wet-lab work,
not yet published.
- CRISPR base editing
- CROP-seq
- Lentiviral transduction
- Cloning
TMT proteomics with internal reference scaling
Training project, University Hospital Frankfurt
Worked through a multi-plex TMT dataset carrying a pooled reference channel and
deliberate plex-level batch differences, to show why internal reference scaling is
required before any cross-plex comparison is meaningful.
Documented as a reproducible walkthrough.
Repository
flowGateR
Independent tool
Scripted gating workflow for flow cytometry in R, written to make gating decisions
explicit and repeatable rather than clicked through by hand in a GUI.
Grew out of several years on FACSCanto and LSRFortessa.
- R
- Flow cytometry
- Reproducibility
Repository
Mitochondrial DNA NGS workflow
Training project, CQ Mplus Academy, Berlin
Snakemake workflow for mtDNA sequencing from blood samples, covering read processing
through variant calling with the steps and dependencies declared rather than implied.
Reusable across sample batches.
Repository