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omero-integration
// Microscopy data management platform. Access images via Python, retrieve datasets, analyze pixels, manage ROIs/annotations, batch processing, for high-content screening and microscopy workflows.
// Microscopy data management platform. Access images via Python, retrieve datasets, analyze pixels, manage ROIs/annotations, batch processing, for high-content screening and microscopy workflows.
Deep generative models for single-cell omics. Use when you need probabilistic batch correction (scVI), transfer learning, differential expression with uncertainty, or multi-modal integration (TOTALVI, MultiVI). Best for advanced modeling, batch effects, multimodal data. For standard analysis pipelines use scanpy.
Biological data toolkit. Sequence analysis, alignments, phylogenetic trees, diversity metrics (alpha/beta, UniFrac), ordination (PCoA), PERMANOVA, FASTA/Newick I/O, for microbiome analysis.
Modal is a serverless cloud platform for running Python on demand, including on-demand GPUs. Use when deploying or serving AI/ML models, running GPU-accelerated workloads (training, fine-tuning, inference), serving web endpoints, scheduling batch jobs, or scaling Python code to cloud containers with the Modal SDK.
End-to-end bulk RNA-seq orchestrator — takes raw FASTQ reads through QC and trimming (FastQC, fastp/Trim Galore), alignment and quantification (STAR, Salmon, featureCounts), assembles a gene-level counts matrix, then hands off to differential expression (pydeseq2), pathway/GSEA enrichment (pathway-enrichment), and publication figures (scientific-visualization). Use whenever the user has bulk RNA-seq reads or quant output and wants a complete, reproducible differential-expression workflow — e.g. "analyze my RNA-seq", "FASTQ to DESeq2", "run nf-core/rnaseq", "STAR/Salmon quantification", "build a counts matrix for DESeq2", or "go from reads to differentially expressed genes and enriched pathways". Routes between an nf-core/rnaseq (Nextflow) path and a standalone STAR/Salmon path, and covers experimental design, strandedness, and QC gates. For single-cell RNA-seq use the scanpy skill instead.
Run pathway and gene-set enrichment analysis on gene lists or ranked gene data, then interpret the results. Use whenever the user has a set of genes (differentially expressed genes from PyDESeq2/Scanpy, CRISPR-screen hits, cluster marker genes, proteomics hits) and wants to know which biological pathways, GO terms, or gene sets are over-represented or enriched. Covers over-representation analysis (ORA / Enrichr / Fisher / hypergeometric), ranked Gene Set Enrichment Analysis (GSEA / preranked), single-sample scoring (ssGSEA/GSVA), and functional profiling via gseapy, g:Profiler, Enrichr libraries, MSigDB, GO, KEGG, Reactome, and WikiPathways — plus gene-ID mapping, choosing the right background universe, multiple-testing correction, redundancy reduction, dotplots/enrichment maps, and publication-ready tables. Use this for "pathway analysis", "enrichment analysis", "GO enrichment", "KEGG/Reactome pathways", "GSEA", "over-representation", "functional annotation", or "what pathways are my genes in".
Build, run, and debug Nextflow data pipelines and nf-core workflows end to end. Use whenever the user mentions Nextflow, nf-core, .nf files, nextflow.config, DSL2, processes/channels/operators, samplesheets, or wants to run a community pipeline (e.g. nf-core/rnaseq, nf-core/sarek), write or test a module/subworkflow with nf-test, configure executors/containers (Docker, Singularity/Apptainer, Conda, Wave), scale a workflow to HPC/SLURM or cloud (AWS Batch, Google Batch, Azure, Kubernetes), or debug a failed/-resume run. Make sure to use this skill for any reproducible scientific/bioinformatics workflow work even if the user does not say the word "Nextflow", and for authoring nf-core-compliant pipelines, modules, configs, and linting.
| name | omero-integration |
| description | Microscopy data management platform. Access images via Python, retrieve datasets, analyze pixels, manage ROIs/annotations, batch processing, for high-content screening and microscopy workflows. |
| license | Unknown |
| metadata | {"version":"1.0","skill-author":"K-Dense Inc."} |
OMERO is an open-source platform for managing, visualizing, and analyzing microscopy images and metadata. Access images via Python API, retrieve datasets, analyze pixels, manage ROIs and annotations, for high-content screening and microscopy workflows.
This skill should be used when:
This skill covers eight major capability areas. Each is documented in detail in the references/ directory:
File: references/connection.md
Establish secure connections to OMERO servers, manage sessions, handle authentication, and work with group contexts. Use this for initial setup and connection patterns.
Common scenarios:
File: references/data_access.md
Navigate OMERO's hierarchical data structure (Projects → Datasets → Images) and screening data (Screens → Plates → Wells). Retrieve objects, query by attributes, and access metadata.
Common scenarios:
File: references/metadata.md
Create and manage annotations including tags, key-value pairs, file attachments, and comments. Link annotations to images, datasets, or other objects.
Common scenarios:
File: references/image_processing.md
Access raw pixel data as NumPy arrays, manipulate rendering settings, create derived images, and manage physical dimensions.
Common scenarios:
File: references/rois.md
Create, retrieve, and analyze ROIs with various shapes (rectangles, ellipses, polygons, masks, points, lines). Extract intensity statistics from ROI regions.
Common scenarios:
File: references/tables.md
Store and query structured tabular data associated with OMERO objects. Useful for analysis results, measurements, and metadata.
Common scenarios:
File: references/scripts.md
Create OMERO.scripts that run server-side for batch processing, automated workflows, and integration with OMERO clients.
Common scenarios:
File: references/advanced.md
Covers permissions, filesets, cross-group queries, delete operations, and other advanced functionality.
Common scenarios:
uv pip install omero-py
Requirements:
Basic connection pattern:
from omero.gateway import BlitzGateway
# Connect to OMERO server
conn = BlitzGateway(username, password, host=host, port=port)
connected = conn.connect()
if connected:
# Perform operations
for project in conn.listProjects():
print(project.getName())
# Always close connection
conn.close()
else:
print("Connection failed")
Recommended pattern with context manager:
from omero.gateway import BlitzGateway
with BlitzGateway(username, password, host=host, port=port) as conn:
# Connection automatically managed
for project in conn.listProjects():
print(project.getName())
# Automatically closed on exit
For data exploration:
references/connection.md to establish connectionreferences/data_access.md to navigate hierarchyreferences/metadata.md for annotation detailsFor image analysis:
references/image_processing.md for pixel data accessreferences/rois.md for region-based analysisreferences/tables.md to store resultsFor automation:
references/scripts.md for server-side processingreferences/data_access.md for batch data retrievalFor advanced operations:
references/advanced.md for permissions and deletionreferences/connection.md for cross-group queriesreferences/connection.md)references/data_access.md)references/data_access.md)references/image_processing.md)references/tables.md or references/metadata.md)references/rois.md)references/rois.md)references/tables.md)references/scripts.md)Always wrap OMERO operations in try-except blocks and ensure connections are properly closed:
from omero.gateway import BlitzGateway
import traceback
try:
conn = BlitzGateway(username, password, host=host, port=port)
if not conn.connect():
raise Exception("Connection failed")
# Perform operations
except Exception as e:
print(f"Error: {e}")
traceback.print_exc()
finally:
if conn:
conn.close()