Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
日本語の概要は準備中です。原文の説明を表示しています。
Automated and marker-guided single-cell cell type annotation using CellTypist, marker review, reference transfer, and confidence-aware label curation.
インストールする前に、エージェントに与えられる指示の中身を確認できます。
Reference examples assume:
scanpy 1.10+celltypist 1.6+pandas 2.2+Before using code patterns, verify installed versions match the environment:
python -c "import scanpy, celltypist; print(scanpy.__version__, celltypist.__version__)"Use this skill when the user wants cluster labels or per-cell labels for scRNA-seq. The default stance is:
Unknown, Uncertain, or Ambiguous when evidence is weak.h5ad with clusters and embeddingsresults/annotated.h5adresults/cell_labels.tsvresults/cluster_annotation_summary.tsvfigures/umap_cell_types.pdffigures/marker_dotplot.pdfscanpycelltypistpandasmatplotlibimport scanpy as sc
import celltypist
adata = sc.read_h5ad("results/processed.h5ad")
pred = celltypist.annotate(adata, model="Immune_All_Low.pkl", majority_voting=True)
adata = pred.to_adata()
adata.obs["cell_type_raw"] = adata.obs["majority_voting"]
adata.obs["cell_type_confidence"] = adata.obs["conf_score"]
adata.write("results/annotated.h5ad")
Check canonical lineage markers on UMAP, dotplots, or heatmaps. If clusters do not support a plausible biological separation, do not lock in labels yet.
Use CellTypist or another compatible reference transfer method. Store:
Review top markers per cluster and compare them against predicted labels. Rename or collapse labels if fine categories are not robust.
At minimum, keep:
cell_type_rawcell_type_confidencecell_type_finalresults/annotated.h5adresults/cell_labels.tsvresults/cluster_annotation_summary.tsvfigures/umap_cell_types.pdffigures/marker_dotplot.pdfCellTypist conf_score > 0.5 is usually comfortable for a provisional label.0.2-0.5 should be manually reviewed against markers.< 0.2 should usually remain Unknown or Uncertain unless markers are compelling.scanpyscvi-toolsまだレビューはありません。使ってみた感想をお寄せください。
概要と使いどころ
Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
日本語の概要は準備中です。原文の説明を表示しています。
Validate protein designs using AlphaFold2 structure prediction. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm. For QC thresholds, use protein-qc.
日本語の概要は準備中です。原文の説明を表示しています。
AlphaFold2 / AlphaFold-Multimer structure prediction for validation and confidence scoring. Use this skill when: (1) Validating designed sequences fold correctly, (2) Predicting binder-target complex structures, (3) Calculating confidence metrics (pLDDT, pTM, ipTM), (4) Self-consistency validation of designs, (5) Multi-chain complex prediction with AlphaFold-Multimer. For faster single-chain prediction, use esm2-sequence-scoring. For QC thresholds, use protein-design-qc.
日本語の概要は準備中です。原文の説明を表示しています。
Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
日本語の概要は準備中です。原文の説明を表示しています。
ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
日本語の概要は準備中です。原文の説明を表示しています。
End-to-end binder design using BindCraft hallucination. Use this skill when: (1) Designing protein binders with built-in AF2 validation, (2) Running production-quality binder campaigns, (3) Using different design protocols (fast, default, slow), (4) Need joint backbone and sequence optimization, (5) Want high experimental success rate. For backbone-only generation, use rfdiffusion. For QC thresholds, use protein-qc. For tool selection guidance, use binder-design.
日本語の概要は準備中です。原文の説明を表示しています。