Christian Panse avatar

Christian Panse

Community

@cpanse · 47N 008E

53Followers
|
129Public Repos
|
37Published Skills

proteome informatics; ms comp; visualization; maps; code; reproducible research @[email protected]

Skills Distribution
DomainData Systems...Single-Cell & Spat.. (45%)LIMS & Data Proven.. (20%)HPC & Infrastructu.. (15%)Genomics Pipeline .. (12%)

Agent Skills by Christian Panse

Showing 37 vetted skills indexed across 1 GitHub repositories.

cpansecpanse

bfabric-query

Query and trace lineage of projects, samples, and datasets in B-Fabric LIMS.

Community
Intermediate
cpansecpanse

bfabric-tools

Registers datasets and queries project metadata in B-Fabric LIMS via btools CLI and Python API.

Community
Intermediate
cpansecpanse

skill-audit

Lints SKILL.md files and scripts for credentials, broken references, and convention violations.

Community
Advanced
cpansecpanse

fgcz-context

Provides canonical institutional context for FGCZ infrastructure, tools, and conventions.

Community
Basic
cpansecpanse

multi-llm-review

Orchestrates parallel multi-LLM reviews of fgcz-skills plugins and aggregates findings by agreement strength.

Community
Advanced
cpansecpanse

sample2barcode-generation

Generate Sample2Barcode CSV files for CellRanger multi demultiplexing on FGCZ SUSHI infrastructure.

Community
Intermediate
cpansecpanse

mixcr-analysis

Analyze bulk TCR and BCR repertoires from amplicon FASTQ data using MiXCR.

Community
Advanced
cpansecpanse

draugr-demultiplexing

Automates and troubleshoots sequencing run demultiplexing via draugr, B-Fabric, and bcl2fastq.

Community
Advanced
cpansecpanse

genome-reference-build

Build and deploy genome references on FGCZ infrastructure using ezRun conventions.

Community
Advanced
cpansecpanse

spaceranger-fgcz

Runs SpaceRanger for Visium and VisiumHD spatial transcriptomics on FGCZ SUSHI infrastructure.

Community
Advanced
cpansecpanse

nextflow-development

Run nf-core pipelines for RNA-seq, WGS/WES, and ATAC-seq analysis on local or GEO/SRA sequencing data.

Community
Advanced
cpansecpanse

rapids-gpu-analysis

Accelerate single-cell and spatial transcriptomics analysis on NVIDIA GPUs using rapids_singlecell.

Community
Advanced
cpansecpanse

cytetype-annotation

Annotate cell types in clustered Seurat objects using the CyteTypeR API.

Community
Advanced
cpansecpanse

scvi-tools

Train deep generative models for single-cell integration, annotation, and multi-modal analysis with scvi-tools.

Community
Advanced
cpansecpanse

rctd-py

Runs GPU-accelerated RCTD cell type deconvolution on spatial transcriptomics data via Python.

Community
Advanced
cpansecpanse

scevan-analysis

Identifies malignant cells in scRNA-seq data via CNV analysis with SCEVAN on FGCZ infrastructure.

Community
Intermediate
cpansecpanse

seurat-analysis

Analyze single-cell and spatial transcriptomics data with Seurat v5 on FGCZ infrastructure.

Community
Advanced
cpansecpanse

cytotrace2-analysis

Predict cellular potency and differentiation states from scRNA-seq Seurat objects using CytoTRACE2.

Community
Advanced
cpansecpanse

xenium-ccf-registration

Registers 10x Xenium spatial transcriptomics sections to the Allen Brain CCFv3 atlas using STalign LDDMM alignment.

Community
Advanced
cpansecpanse

slingshot-trajectory

Infer differentiation trajectories and pseudotime from Seurat v5 single-cell data using Slingshot.

Community
Advanced
cpansecpanse

insitucnv-analysis

Detect copy number variations and tumor subclones in Xenium spatial transcriptomics data using infercnvpy.

Community
Advanced
cpansecpanse

scomatic-analysis

Detect somatic mutations in single-cell RNA-seq and ATAC-seq data using the SComatic pipeline.

Community
Advanced
cpansecpanse

clusterprofiler-pathways

Performs GO, KEGG, and GSEA enrichment analysis on single-cell DEG lists using clusterProfiler.

Community
Intermediate
cpansecpanse

cellchat-analysis

Infer and compare cell-cell communication networks from single-cell RNA-seq data using CellChat.

Community
Advanced

Frequently Asked Questions About Christian Panse

FAQPage Schema
What tasks can I accomplish with cpanse's FGCZ skills?

You can process 10x Genomics data with CellRanger, run nf-core pipelines, perform Seurat/scVI/RCTD single-cell and spatial analysis, detect CNVs and somatic mutations, query B-Fabric LIMS for lineage, submit SUSHI jobs, deploy ShinyProxy apps, and render self-correcting R Markdown reports.

Who are these skills designed for?

Bioinformaticians, computational biologists, and core-facility staff at FGCZ or similar genomics centers. Personas include single-cell analysts running Seurat/scvi-tools, spatial transcriptomics researchers using Visium/Xenium, LIMS administrators managing B-Fabric metadata, and developers building SUSHI apps with ezRun and Ruby on Rails.

How do the skills run in practice on FGCZ infrastructure?

Skills execute on FGCZ's SLURM cluster using Lmod modules, SBATCH GPU templates for L40S nodes, and pixi environments. Jobs are submitted via SUSHI apps or sushi_fabric commands, datasets flow through B-Fabric and gStore, and reports render as R Markdown with automated retry-and-validate loops.

What prerequisites and dependencies are required?

Access to FGCZ infrastructure: B-Fabric credentials, gitlab.bfabric.org PAT authentication, SLURM compute nodes, and Lmod modules for R, Python, and CellRanger. Specific skills require Seurat v5, scvi-tools, infercnvpy, spacexr, MiXCR, or NVIDIA GPUs; genome reference builds must run on fgcz-r-029.

How is quality and consistency enforced across the skill marketplace?

The skill-audit linter deterministically detects plaintext credentials, personal paths, broken references, and version drift in CI or pre-commit hooks. The multi-llm-review skill then runs parallel Claude, Codex, and Cursor reviews with per-finding agreement scoring to catch remaining semantic issues.