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。
Designs experiments to minimize and account for batch effects using balanced layouts and blocking strategies. Use when planning multi-batch experiments, assigning samples to sequencing lanes, or designing studies where technical variation could confound biological signals.
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Reference examples tested with: limma 3.58+
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.
"Design experiment to avoid batch effects" → Plan sample-to-batch assignments that confound biology with technical variation, and apply correction methods post-hoc.
sva::ComBat(), limma::removeBatchEffect()scanpy.pp.combat() for single-cell dataBatch effects are unavoidable. Good design makes them correctable.
# BAD: Confounded design
# Batch 1: All treated samples
# Batch 2: All control samples
# -> Cannot separate batch from treatment
# GOOD: Balanced design
# Batch 1: 3 treated, 3 control
# Batch 2: 3 treated, 3 control
# -> Batch effect can be estimated and removed
library(designit)
# Create balanced assignment
samples <- data.frame(
sample_id = paste0('S', 1:24),
condition = rep(c('ctrl', 'treat'), each = 12),
sex = rep(c('M', 'F'), 12)
)
# Optimize batch assignment
batch_design <- osat(samples, batch_size = 8,
balance_cols = c('condition', 'sex'))
Goal: Identify hidden batch effects in expression data by estimating surrogate variables that capture unmodeled technical variation.
Approach: Fit a model matrix for the biological variable, estimate the number of surrogate variables using num.sv, then compute surrogate variables with sva for inclusion in downstream differential analysis.
library(sva)
# From count matrix
mod <- model.matrix(~condition, colData)
mod0 <- model.matrix(~1, colData)
# Estimate number of surrogate variables (hidden batches)
n_sv <- num.sv(counts_normalized, mod)
# Estimate surrogate variables
svobj <- sva(counts_normalized, mod, mod0, n.sv = n_sv)
| Method | When to Use |
|---|---|
| ComBat | Known batches, moderate effects |
| SVA | Unknown batches, exploratory |
| RUVseq | Using control genes |
| limma::removeBatchEffect | Visualization only |
Always record:
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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。