Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Detect and remove doublets from flow and mass cytometry data. Covers FSC/SSC gating and computational doublet detection methods. Use when filtering out cell aggregates before clustering or quantitative analysis.
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설치 방법 보기설치하기 전에 에이전트에게 전달되는 지시 내용을 확인할 수 있습니다.
Reference examples tested with: flowCore 2.14+, ggplot2 3.5+
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.
"Remove doublets from my flow cytometry data" → Detect and filter out cell aggregates using FSC-A/FSC-H gating or computational methods before clustering or quantitative analysis.
flowCore rectangular gates on FSC-A vs FSC-Hlibrary(flowCore)
library(ggcyto)
# Load data
fs <- read.flowSet(list.files('data/', pattern = '\\.fcs$', full.names = TRUE))
# FSC-A vs FSC-H for doublet discrimination
# Singlets fall on diagonal, doublets have higher FSC-A for given FSC-H
# Manual rectangular gate
singlet_gate <- rectangleGate(
filterId = 'singlets',
'FSC-A' = c(50000, 250000),
'FSC-H' = c(50000, 250000)
)
# Or use polygon gate for diagonal
singlet_polygon <- polygonGate(
filterId = 'singlets',
.gate = data.frame(
'FSC-A' = c(50000, 250000, 250000, 50000),
'FSC-H' = c(40000, 200000, 260000, 60000)
)
)
# Apply gate
singlets <- Subset(fs, singlet_gate)
# Visualize
autoplot(fs[[1]], 'FSC-A', 'FSC-H') + geom_gate(singlet_gate)
library(flowDensity)
# Automatic singlet gate
singlet_result <- flowDensity(
fs[[1]],
channels = c('FSC-A', 'FSC-H'),
position = c(TRUE, TRUE),
gates = c(NA, NA)
)
# Get gated population
singlets <- getflowFrame(singlet_result)
# Percentage singlets
pct_singlets <- nrow(singlets) / nrow(fs[[1]]) * 100
cat('Singlets:', round(pct_singlets, 1), '%\n')
library(flowAI)
# flowAI performs comprehensive QC including:
# - Flow rate anomaly detection
# - Signal acquisition anomaly detection
# - Dynamic range anomaly detection
# Run flowAI
fs_qc <- flow_auto_qc(
fs,
folder_results = 'flowAI_results',
fcs_QC = TRUE,
fcs_highQ = TRUE
)
# Results include singlet detection based on flow rate stability
# Some instruments provide FSC-W (width) instead of FSC-H
# FSC-A = FSC-H × FSC-W
# Doublets have higher width
if ('FSC-W' %in% colnames(fs[[1]])) {
singlet_gate_w <- rectangleGate(
filterId = 'singlets',
'FSC-A' = c(50000, 250000),
'FSC-W' = c(50000, 100000) # Lower width = singlets
)
singlets <- Subset(fs, singlet_gate_w)
}
# Calculate FSC-A/FSC-H ratio
# Singlets have ratio close to constant (based on pulse geometry)
# Doublets have elevated ratio
calculate_fsc_ratio <- function(ff) {
fsc_a <- exprs(ff)[, 'FSC-A']
fsc_h <- exprs(ff)[, 'FSC-H']
ratio <- fsc_a / (fsc_h + 1) # Add small value to avoid division by zero
return(ratio)
}
# Add ratio as derived parameter
for (i in 1:length(fs)) {
ratio <- calculate_fsc_ratio(fs[[i]])
fs[[i]] <- cbind2(fs[[i]], ratio)
colnames(fs[[i]])[ncol(fs[[i]])] <- 'FSC_ratio'
}
# Gate on ratio
ratio_cutoff <- quantile(exprs(fs[[1]])[, 'FSC_ratio'], 0.95)
singlet_gate_ratio <- rectangleGate(filterId = 'singlets', 'FSC_ratio' = c(0, ratio_cutoff))
# For cell types where FSC doesn't discriminate well,
# use SSC-A vs SSC-H additionally
ssc_singlet_gate <- rectangleGate(
filterId = 'ssc_singlets',
'SSC-A' = c(10000, 200000),
'SSC-H' = c(10000, 200000)
)
# Combine FSC and SSC gates
combined_gate <- singlet_gate & ssc_singlet_gate
singlets <- Subset(fs, combined_gate)
library(CATALYST)
# For CyTOF data, use DNA channels or event length
# DNA-based doublet detection (if DNA channels present)
# Doublets have ~2x DNA content
sce <- prepData(fs, panel, md)
# If Event_length channel exists
if ('Event_length' %in% rownames(sce)) {
event_length <- assay(sce)['Event_length', ]
singlet_idx <- event_length < quantile(event_length, 0.95)
sce_singlets <- sce[, singlet_idx]
cat('Removed', sum(!singlet_idx), 'doublets based on event length\n')
}
# DNA intercalator method
if (all(c('DNA1', 'DNA2') %in% rownames(sce))) {
dna_total <- assay(sce)['DNA1', ] + assay(sce)['DNA2', ]
dna_cutoff <- quantile(dna_total, 0.95)
singlet_idx <- dna_total < dna_cutoff
sce_singlets <- sce[, singlet_idx]
}
Goal: Detect and remove cell doublets from a CyTOF/flow dataset using a regression-based approach on scatter parameters.
Approach: Model the expected FSC-A vs FSC-H relationship for singlets with linear regression, classify events with large residuals (above the 95th percentile) as doublets, and filter them out.
library(CATALYST)
# Load and prepare data
sce <- prepData(fs, panel, md, transform = TRUE, cofactor = 5)
# Remove doublets using marker-based method
sce <- filterSCE(sce, !is_doublet(sce))
# Custom doublet detection based on FSC
fsc_a <- colData(sce)$FSC_A
fsc_h <- colData(sce)$FSC_H
# Model expected singlet relationship
fit <- lm(fsc_a ~ fsc_h)
residuals <- abs(fsc_a - predict(fit))
threshold <- quantile(residuals, 0.95)
# Mark doublets
colData(sce)$doublet <- residuals > threshold
sce_singlets <- sce[, !colData(sce)$doublet]
cat('Doublet rate:', round(mean(colData(sce)$doublet) * 100, 1), '%\n')
# Process all samples
detect_doublets <- function(ff, method = 'fsc') {
if (method == 'fsc') {
fsc_a <- exprs(ff)[, 'FSC-A']
fsc_h <- exprs(ff)[, 'FSC-H']
fit <- lm(fsc_a ~ fsc_h)
residuals <- abs(fsc_a - predict(fit))
threshold <- quantile(residuals, 0.95)
singlet_idx <- residuals <= threshold
} else if (method == 'ratio') {
ratio <- exprs(ff)[, 'FSC-A'] / (exprs(ff)[, 'FSC-H'] + 1)
singlet_idx <- ratio < quantile(ratio, 0.95)
}
return(ff[singlet_idx, ])
}
# Apply to all samples
fs_singlets <- fsApply(fs, detect_doublets, method = 'fsc')
# Report
doublet_rates <- sapply(1:length(fs), function(i) {
1 - nrow(fs_singlets[[i]]) / nrow(fs[[i]])
})
cat('Mean doublet rate:', round(mean(doublet_rates) * 100, 1), '%\n')
library(ggplot2)
# Extract data for plotting
plot_data <- data.frame(
FSC_A = exprs(fs[[1]])[, 'FSC-A'],
FSC_H = exprs(fs[[1]])[, 'FSC-H']
)
# Calculate doublet status
fit <- lm(FSC_A ~ FSC_H, data = plot_data)
plot_data$residual <- abs(plot_data$FSC_A - predict(fit))
plot_data$doublet <- plot_data$residual > quantile(plot_data$residual, 0.95)
# Plot
ggplot(plot_data, aes(x = FSC_H, y = FSC_A, color = doublet)) +
geom_point(alpha = 0.3, size = 0.5) +
scale_color_manual(values = c('gray', 'red')) +
theme_bw() +
labs(title = 'Doublet Detection', x = 'FSC-H', y = 'FSC-A')
ggsave('doublet_detection.png', width = 8, height = 6)
Workflow order: cytometry-qc → doublet-detection → bead-normalization → clustering
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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.