Workflow for read alignment, sorting, indexing, mapping statistics, and downstream-ready alignment artifacts.
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Perform differential expression analysis of miRNAs between conditions using DESeq2 or edgeR with small RNA-specific considerations. Use when identifying miRNAs that change between treatment groups, disease states, or developmental stages.
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실행 점수 미검증
설치 방법 보기설치하기 전에 에이전트에게 전달되는 지시 내용을 확인할 수 있습니다.
Reference examples tested with: DESeq2 1.42+, edgeR 4.0+, ggplot2 3.5+, 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.
"Find differentially expressed miRNAs between my conditions" → Perform statistical testing on miRNA count matrices to identify miRNAs with significant expression changes, accounting for small RNA-specific normalization considerations.
DESeq2::DESeq() or edgeR::glmQLFTest() on miRNA count datalibrary(DESeq2)
# Load miRge3 or miRDeep2 counts
counts <- read.csv('miR.Counts.csv', row.names = 1)
# Create sample metadata
coldata <- data.frame(
sample = colnames(counts),
condition = factor(c('control', 'control', 'treated', 'treated')),
row.names = colnames(counts)
)
Goal: Identify miRNAs with significant expression changes between experimental conditions, accounting for small RNA-specific normalization.
Approach: Create a DESeqDataSet from miRNA counts, filter low-expressed miRNAs using a lower threshold than mRNA (10 reads total), run the DESeq2 pipeline, and extract results with BH-corrected p-values.
# Create DESeq2 dataset
dds <- DESeqDataSetFromMatrix(
countData = round(counts), # DESeq2 requires integers
colData = coldata,
design = ~ condition
)
# Filter low-expressed miRNAs
# miRNAs typically have fewer total counts than mRNAs
# Keep miRNAs with at least 10 reads across samples
keep <- rowSums(counts(dds)) >= 10
dds <- dds[keep, ]
# Run DESeq2
dds <- DESeq(dds)
# Get results
res <- results(dds, contrast = c('condition', 'treated', 'control'))
res <- res[order(res$padj), ]
# apeglm shrinkage for more accurate log2 fold changes
# Particularly important for low-count miRNAs
library(apeglm)
res_shrunk <- lfcShrink(
dds,
coef = 'condition_treated_vs_control',
type = 'apeglm'
)
# Standard thresholds for miRNA DE
# padj < 0.05: FDR-corrected significance
# |log2FC| > 1: 2-fold change minimum
sig <- subset(res_shrunk, padj < 0.05 & abs(log2FoldChange) > 1)
sig <- sig[order(sig$padj), ]
# Separate up and down-regulated
up <- subset(sig, log2FoldChange > 0)
down <- subset(sig, log2FoldChange < 0)
cat('Upregulated:', nrow(up), '\n')
cat('Downregulated:', nrow(down), '\n')
library(edgeR)
# Create DGEList
dge <- DGEList(counts = counts, group = coldata$condition)
# Filter low expression
keep <- filterByExpr(dge)
dge <- dge[keep, , keep.lib.sizes = FALSE]
# Normalize
dge <- calcNormFactors(dge)
# Design matrix
design <- model.matrix(~ condition, data = coldata)
# Estimate dispersion
dge <- estimateDisp(dge, design)
# Fit model and test
fit <- glmQLFit(dge, design)
qlf <- glmQLFTest(fit, coef = 2)
# Get results
res_edger <- topTags(qlf, n = Inf)$table
library(ggplot2)
library(EnhancedVolcano)
# Volcano plot
EnhancedVolcano(
res_shrunk,
lab = rownames(res_shrunk),
x = 'log2FoldChange',
y = 'padj',
pCutoff = 0.05,
FCcutoff = 1,
title = 'Differential miRNA Expression'
)
# MA plot
plotMA(res_shrunk, ylim = c(-4, 4))
library(pheatmap)
# Get normalized counts
vsd <- vst(dds, blind = FALSE)
# Select significant miRNAs
sig_mirnas <- rownames(sig)
mat <- assay(vsd)[sig_mirnas, ]
# Z-score scale rows
mat_scaled <- t(scale(t(mat)))
pheatmap(
mat_scaled,
annotation_col = coldata['condition'],
cluster_rows = TRUE,
cluster_cols = TRUE,
show_rownames = nrow(mat) < 50
)
# Full results with normalized counts
res_df <- as.data.frame(res_shrunk)
res_df$miRNA <- rownames(res_df)
res_df$baseMean_norm <- rowMeans(counts(dds, normalized = TRUE)[rownames(res_df), ])
write.csv(res_df, 'DE_miRNAs_full.csv', row.names = FALSE)
# Significant only
write.csv(as.data.frame(sig), 'DE_miRNAs_significant.csv')
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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.
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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.
한국어 요약은 준비 중입니다. 원문 설명을 표시하고 있습니다.