Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Unsupervised clustering and cell type identification for flow/mass cytometry. Covers FlowSOM, Phenograph, and CATALYST workflows. Use when discovering cell populations in high-dimensional cytometry data without predefined gates.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
설치 방법 보기설치하기 전에 에이전트에게 전달되는 지시 내용을 확인할 수 있습니다.
Reference examples tested with: FlowSOM 2.10+, scanpy 1.10+
Before using code patterns, verify installed versions match. If versions differ:
packageVersion('<pkg>') then ?function_name to verify parametersIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Cluster my cytometry data to find cell types" → Discover cell populations in high-dimensional flow/mass cytometry data using unsupervised clustering without predefined gates.
FlowSOM::FlowSOM() for self-organizing map clusteringCATALYST::cluster() with Phenograph or FlowSOMGoal: Cluster cytometry events into cell populations using self-organizing maps.
Approach: Build a FlowSOM grid on marker channels, then extract metacluster assignments per cell.
library(FlowSOM)
# Prepare data
expr <- exprs(fcs)
marker_cols <- grep('CD|HLA', colnames(fcs), value = TRUE)
# Build SOM
fsom <- FlowSOM(fcs,
colsToUse = marker_cols,
xdim = 10, ydim = 10,
nClus = 20,
seed = 42)
# Get cluster assignments
clusters <- GetMetaclusters(fsom)
# Add to flowFrame
exprs(fcs) <- cbind(exprs(fcs), cluster = clusters)
Goal: Run the complete CATALYST clustering pipeline from flowSet to annotated cell populations.
Approach: Convert flowSet to SingleCellExperiment with prepData, then cluster on type markers with FlowSOM via CATALYST.
library(CATALYST)
library(SingleCellExperiment)
# Create SCE from flowSet
sce <- prepData(fs, panel, md, transform = TRUE, cofactor = 5)
# Clustering
sce <- cluster(sce,
features = 'type', # Use 'type' markers from panel
xdim = 10, ydim = 10,
maxK = 20,
seed = 42)
# View cluster assignments
table(cluster_ids(sce, 'meta20'))
Goal: Identify cell populations using graph-based community detection on marker expression.
Approach: Build a k-nearest-neighbor graph on type markers, then partition with Louvain community detection via Rphenograph.
library(Rphenograph)
# Extract expression matrix
expr <- assay(sce, 'exprs')
# Run Phenograph
pheno_result <- Rphenograph(t(expr[rowData(sce)$marker_class == 'type', ]), k = 30)
# Get clusters
sce$phenograph <- factor(membership(pheno_result[[2]]))
Goal: Project high-dimensional cytometry data into 2D for visualization of cell populations.
Approach: Run UMAP or tSNE on type marker channels using CATALYST's runDR wrapper, then plot colored by cluster.
# UMAP
sce <- runDR(sce, dr = 'UMAP', features = 'type')
# tSNE
sce <- runDR(sce, dr = 'TSNE', features = 'type')
# Plot
plotDR(sce, 'UMAP', color_by = 'meta20')
Goal: Assign cell type labels to clusters based on marker expression profiles.
Approach: Visualize median marker expression per cluster with a heatmap, then map cluster IDs to cell type names.
# Heatmap of marker expression by cluster
plotExprHeatmap(sce, features = 'type',
by = 'cluster_id', k = 'meta20',
scale = 'first', row_anno = FALSE)
# Manual annotation
cluster_annotation <- c(
'1' = 'CD4 T cells',
'2' = 'CD8 T cells',
'3' = 'B cells',
'4' = 'NK cells',
'5' = 'Monocytes'
)
sce$cell_type <- cluster_annotation[as.character(cluster_ids(sce, 'meta20'))]
Goal: Reduce overclustering by merging similar clusters into biologically meaningful groups.
Approach: Define a mapping table from original to merged cluster IDs, then apply with CATALYST's mergeClusters.
# Merge similar clusters
merging_table <- data.frame(
original = 1:20,
merged = c(1, 1, 2, 2, 3, 3, 4, 4, 5, 5,
6, 6, 7, 7, 8, 8, 9, 9, 10, 10)
)
sce <- mergeClusters(sce, k = 'meta20', table = merging_table, id = 'merged')
Goal: Quantify the relative frequency of each cell population across samples and conditions.
Approach: Cross-tabulate cluster assignments by sample ID, convert to proportions, and plot grouped by condition.
# Cluster frequencies per sample
abundances <- table(cluster_ids(sce, 'meta20'), sce$sample_id)
freq <- prop.table(abundances, margin = 2)
# Plot
plotAbundances(sce, k = 'meta20', by = 'cluster_id', group_by = 'condition')
Goal: Summarize and compare marker expression levels across clusters and conditions.
Approach: Plot per-cluster median expression with CATALYST's plotClusterExprs and pseudo-bulk expression faceted by cluster.
# Median expression per cluster
plotClusterExprs(sce, k = 'meta20', features = 'type')
# Expression by cluster and condition
plotPbExprs(sce, k = 'meta20', features = 'type', facet_by = 'cluster_id')
Goal: Save clustering results and annotated SCE object for downstream analysis or sharing.
Approach: Extract cluster assignments into colData, export as CSV, and serialize the full SCE as RDS.
# Add cluster info to metadata
colData(sce)$cluster <- cluster_ids(sce, 'meta20')
# Export to CSV
results <- as.data.frame(colData(sce))
write.csv(results, 'clustering_results.csv', row.names = FALSE)
# Save SCE
saveRDS(sce, 'sce_clustered.rds')
Goal: Determine the optimal number of metaclusters for the dataset.
Approach: Compare normalized reduction stability (NRS) plots and heatmaps at different K values to find where clusters remain distinct.
# Delta area plot
plotNRS(sce, features = 'type')
# Or visual inspection of heatmap at different K
plotExprHeatmap(sce, features = 'type', by = 'cluster_id', k = 'meta10')
plotExprHeatmap(sce, features = 'type', by = 'cluster_id', k = 'meta20')
Goal: Remove batch effects from cytometry data before or after clustering.
Approach: Detect batch effects by coloring UMAP by batch variable, then apply MNN correction with batchelor if needed.
# If batch effects present
library(batchelor)
sce <- runDR(sce, dr = 'UMAP', features = 'type')
# Check for batch effects
plotDR(sce, 'UMAP', color_by = 'batch')
# MNN correction if needed
sce_corrected <- fastMNN(sce, batch = sce$batch)
아직 리뷰가 없습니다. 사용해 본 소감을 남겨 주세요.
로그인 없이 쓸 수 있습니다. 사용 후기, 질문, 작동하지 않은 환경 등을 편하게 남겨 주세요.
아직 댓글이 없습니다. 첫 댓글을 남겨 보세요.
Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
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.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
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.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.
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.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.