Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Read and manipulate Flow Cytometry Standard (FCS) files. Covers loading data, accessing parameters, and basic data exploration. Use when loading and inspecting flow or mass cytometry data before preprocessing.
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Reference examples tested with: flowCore 2.14+, 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.
"Load my FCS files into R or Python" → Read Flow Cytometry Standard (FCS) files, access channel parameters and metadata, and explore event data for downstream analysis.
flowCore::read.FCS() or flowCore::read.flowSet() for multiple filesfcsparser.parse() or FlowCal.io.FCSData()Goal: Read a single FCS file and inspect its parameters and metadata.
Approach: Use flowCore's read.FCS with transformation disabled to load raw data, then examine parameter names and descriptions.
library(flowCore)
# Read single FCS file
fcs <- read.FCS('sample.fcs', transformation = FALSE, truncate_max_range = FALSE)
# File info
print(fcs)
# Parameter names
colnames(fcs) # Short names
pData(parameters(fcs)) # Full metadata including descriptions
Goal: Read a batch of FCS files into a single flowSet container for uniform processing.
Approach: List FCS files from a directory and load them into a flowSet with read.flowSet.
# Read multiple files into flowSet
files <- list.files('data', pattern = '\\.fcs$', full.names = TRUE)
fs <- read.flowSet(files, transformation = FALSE, truncate_max_range = FALSE)
# Sample names
sampleNames(fs)
# Access individual samples
fcs1 <- fs[[1]]
Goal: Extract the expression matrix from a flowFrame for numeric analysis.
Approach: Call exprs() to get the cells-by-channels matrix, then subset or summarize as needed.
# Get expression matrix
expr <- exprs(fcs)
head(expr)
# Dimensions
dim(expr) # cells x channels
# Channel statistics
summary(expr)
# Get specific channels
cd4_expr <- expr[, 'CD4']
Goal: Retrieve channel names, descriptions, and ranges from the FCS parameter table.
Approach: Access the parameters slot via pData(parameters(fcs)) and build a short-name to description mapping.
# Parameter information
params <- pData(parameters(fcs))
print(params)
# Parameter columns:
# - name: short name (e.g., "FL1-A")
# - desc: description (e.g., "CD4")
# - range: max value
# - minRange: min value
# Get channel mapping
channel_map <- setNames(params$desc, params$name)
# Rename using descriptions
rename_channels <- function(fcs) {
params <- pData(parameters(fcs))
new_names <- ifelse(is.na(params$desc) | params$desc == '',
params$name, params$desc)
colnames(fcs) <- new_names
return(fcs)
}
fcs_renamed <- rename_channels(fcs)
# Subset by cells (rows)
fcs_subset <- fcs[1:1000, ]
# Subset by channels (columns)
fcs_markers <- fcs[, c('CD4', 'CD8', 'CD3')]
# Subset by expression values
high_cd4 <- fcs[exprs(fcs)[, 'CD4'] > 1000, ]
# Combine multiple flowSets
fs_combined <- rbind2(fs1, fs2)
# Or concatenate into single flowFrame
all_data <- fsApply(fs, exprs)
all_data <- do.call(rbind, all_data)
# Write single file
write.FCS(fcs, 'output.fcs')
# Write flowSet
write.flowSet(fs, outdir = 'output_dir')
# Add sample annotations
pData(fs) <- data.frame(
name = sampleNames(fs),
condition = c('Control', 'Control', 'Treatment', 'Treatment'),
patient = c('P1', 'P2', 'P1', 'P2')
)
# Access
pData(fs)
library(ggcyto)
# Density plot
autoplot(fcs, 'FSC-A')
# Bivariate plot
autoplot(fcs, 'CD4', 'CD8')
# Multiple samples
autoplot(fs, 'CD4', 'CD8')
# Time parameter check
if ('Time' %in% colnames(fcs)) {
time <- exprs(fcs)[, 'Time']
plot(time, type = 'l', main = 'Acquisition Time')
}
# Event count per file
fsApply(fs, nrow)
# Check for saturated events
saturation <- apply(exprs(fcs), 2, function(x) mean(x == max(x)) * 100)
print(saturation)
# For use with tidyverse
library(tidyverse)
df <- as.data.frame(exprs(fcs))
df$sample <- 'sample1'
# From flowSet
df_all <- fsApply(fs, function(f) {
d <- as.data.frame(exprs(f))
d$sample <- identifier(f)
d
}, simplify = FALSE)
df_all <- bind_rows(df_all)
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Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
中文简介正在准备中。当前显示原文说明。
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.
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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.
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Workflow for event-level and isoform-level splicing analysis with sashimi-ready outputs and splice QC.
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ATAC-seq processing with assay QC, MACS3 peak calling, consensus peak matrices, differential accessibility, and motif or footprint follow-up.
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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.
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