/bio-atac-seq-motif-deviation
Analyze transcription factor motif accessibility variability using chromVAR. Use when identifying which TF motifs show variable accessibility across samples or conditions in ATAC-seq data.
$ npx -y skills add FreedomIntelligence/OpenClaw-Medical-Skills --skill bio-atac-seq-motif-deviation --agent claude-codeHow it fires
How this skill gets triggered: by you, by Claude, or both.
- Fires itselfAuto-invocation. Claude auto-loads it when your prompt matches the work.Auto-invocation is when the right skill fires by itself at the right moment, driven by a FLOW.md router and a hook, instead of you invoking it by name. It is the difference between a skill being installed and a skill actually getting used.Read the full definition →
- You can call itInvoke it directly when you want it.
- Slash command
/bio-atac-seq-motif-deviation
Context preview
The summary Claude sees to decide when to auto-load this skill.
Analyze transcription factor motif accessibility variability using chromVAR. Use when identifying which TF motifs show variable accessibility across samples or conditions in ATAC-seq data.
SKILL.md
bio-atac-seq-motif-deviation.SKILL.mdname: bio-atac-seq-motif-deviation
description: Analyze transcription factor motif accessibility variability using chromVAR. Use when identifying which TF motifs show variable accessibility across samples or conditions in ATAC-seq data.
tool_type: r
primary_tool: chromVAR
Version Compatibility
Reference examples tested with: ggplot2 3.5+, limma 3.58+
Before using code patterns, verify installed versions match. If versions differ:
- R: `packageVersion('<pkg>')` then `?function_name` to verify parameters
If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
Motif Deviation Analysis
**"Which TF motifs show variable accessibility across my samples?"** → Compute per-sample deviation scores for TF motif accessibility to identify regulators driving chromatin state differences.
- R: `chromVAR::computeDeviations(counts, motifs)`
Measure per-sample variability in transcription factor motif accessibility using chromVAR. This identifies TFs whose binding sites show differential accessibility across conditions.
Required Packages
library(chromVAR)
library(motifmatchr)
library(BSgenome.Hsapiens.UCSC.hg38) # or appropriate genome
library(JASPAR2020)
library(TFBSTools)
library(SummarizedExperiment)
Basic Workflow
**Goal:** Run chromVAR to compute per-sample TF motif deviation scores from ATAC-seq peak counts.
**Approach:** Load peak counts into a SummarizedExperiment, correct for GC bias, filter low-quality peaks, match JASPAR motifs, and compute deviation z-scores.
1. Load Peak Counts
library(chromVAR)
library(SummarizedExperiment)
# From count matrix and peak ranges
peaks <- read.table('peaks.bed', col.names = c('chr', 'start', 'end'))
peak_ranges <- GRanges(seqnames = peaks$chr, ranges = IRanges(peaks$start, peaks$end))
counts <- read.table('counts.txt', header = TRUE, row.names = 1)
counts_matrix <- as.matrix(counts)
fragment_counts <- SummarizedExperiment(
assays = list(counts = counts_matrix),
rowRanges = peak_ranges
)2. Add GC Bias Correction
library(BSgenome.Hsapiens.UCSC.hg38)
fragment_counts <- addGCBias(fragment_counts, genome = BSgenome.Hsapiens.UCSC.hg38)
3. Filter Low-Quality Peaks
# min_depth=1500: Minimum total reads per sample. Adjust based on library size.
# min_in_peaks=0.15: Minimum fraction of reads in peaks (FRiP). 0.15 = 15%.
fragment_counts <- filterSamples(fragment_counts, min_depth = 1500, min_in_peaks = 0.15)
# min_count=10: Require peaks with >=10 reads across samples.
# n_samples_frac=0.1: Peak must be detected in >=10% of samples.
fragment_counts <- filterPeaks(fragment_counts, non_overlapping = TRUE,
min_count = 10, n_samples_frac = 0.1)Get Motif Annotations
From JASPAR
library(JASPAR2020)
library(TFBSTools)
library(motifmatchr)
# Get vertebrate motifs from JASPAR
pfm <- getMatrixSet(JASPAR2020, opts = list(collection = 'CORE', tax_group = 'vertebrates'))
# Match motifs to peaks
# p.cutoff=5e-5: Motif match p-value threshold. Lower = more stringent.
motif_ix <- matchMotifs(pfm, fragment_counts, genome = BSgenome.Hsapiens.UCSC.hg38, p.cutoff = 5e-5)
From CIS-BP or Custom PWMs
# Load custom motifs from file
library(universalmotif)
motifs <- read_meme('custom_motifs.meme')
pfm_list <- lapply(motifs, function(m) convert_motifs(m, class = 'TFBSTools-PFMatrix'))
motif_ix <- matchMotifs(pfm_list, fragment_counts, genome = BSgenome.Hsapiens.UCSC.hg38)Compute Deviations
# Compute chromVAR deviation scores
dev <- computeDeviations(object = fragment_counts, annotations = motif_ix)
# Extract deviation scores (z-scores)
deviation_scores <- deviations(dev)
# Extract variability across samples
variability <- computeVariability(dev)
Interpreting Results
Deviation Scores
# Deviation z-scores: positive = more accessible than expected
# Compare across samples
dev_matrix <- deviations(dev)
print(dim(dev_matrix)) # motifs x samples
# Get top variable motifs
var_df <- variability
var_df <- var_df[order(-var_df$variability), ]
head(var_df, 20)
Variability Interpretation
| Variability | Interpretation | |-------------|----------------| | > 2.0 | Highly variable across samples | | 1.0 - 2.0 | Moderately variable | | < 1.0 | Low variability |
Visualization
Deviation Heatmap
library(pheatmap)
# Get top variable motifs
# n_top=50: Number of top variable motifs to display.
n_top <- 50
top_motifs <- head(rownames(var_df), n_top)
top_dev <- deviation_scores[top_motifs, ]
# Add sample annotations
sample_info <- data.frame(
Condition = colData(fragment_counts)$condition,
row.names = colnames(top_dev)
)
pheatmap(top_dev, annotation_col = sample_info, scale = 'row',
clustering_method = 'ward.D2', show_rownames = TRUE)Variability Plot
plotVariability(variability, use_plotly = FALSE)
PCA of Deviation Scores
library(ggplot2)
# PCA on deviation scores
pca <- prcomp(t(deviation_scores), scale. = TRUE)
pca_df <- data.frame(PC1 = pca$x[,1], PC2 = pca$x[,2],
Condition = colData(fragment_counts)$condition)
ggplot(pca_df, aes(x = PC1, y = PC2, color = Condition)) +
geom_point(size = 3) +
theme_minimal() +
labs(title = 'PCA of chromVAR Deviations')Differential Motif Accessibility
**Goal:** Identify TF motifs with significantly different accessibility between experimental groups.
**Approach:** Fit a linear model (limma) to deviation z-scores across groups and extract significant motifs with empirical Bayes moderation.
Compare Two Groups
library(limma)
# Get sample groups
groups <- factor(colData(fragment_counts)$condition)
# Design matrix
design <- model.matrix(~ groups)
# Fit linear model to deviation scores
fit <- lmFit(deviation_scores, design)
fit <- eBayes(fit)
# Get differenti
Read more
name: bio-atac-seq-motif-deviation description: Analyze transcription factor motif accessibility variability using chromVAR. Use when identifying which TF motifs show variable accessibility across samples or conditions in ATAC-seq data. tool_type: r primary_tool: chromVAR
Version Compatibility
Reference examples tested with: ggplot2 3.5+, limma 3.58+
Before using code patterns, verify installed versions match. If versions differ:
- R: `packageVersion('<pkg>')` then `?function_name` to verify parameters
If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
Motif Deviation Analysis
**"Which TF motifs show variable accessibility across my samples?"** → Compute per-sample deviation scores for TF motif accessibility to identify regulators driving chromatin state differences.
- R: `chromVAR::computeDeviations(counts, motifs)`
Measure per-sample variability in transcription factor motif accessibility using chromVAR. This identifies TFs whose binding sites show differential accessibility across conditions.
Required Packages
library(chromVAR) library(motifmatchr) library(BSgenome.Hsapiens.UCSC.hg38) # or appropriate genome library(JASPAR2020) library(TFBSTools) library(SummarizedExperiment)
Basic Workflow
**Goal:** Run chromVAR to compute per-sample TF motif deviation scores from ATAC-seq peak counts.
**Approach:** Load peak counts into a SummarizedExperiment, correct for GC bias, filter low-quality peaks, match JASPAR motifs, and compute deviation z-scores.
1. Load Peak Counts
library(chromVAR)
library(SummarizedExperiment)
# From count matrix and peak ranges
peaks <- read.table('peaks.bed', col.names = c('chr', 'start', 'end'))
peak_ranges <- GRanges(seqnames = peaks$chr, ranges = IRanges(peaks$start, peaks$end))
counts <- read.table('counts.txt', header = TRUE, row.names = 1)
counts_matrix <- as.matrix(counts)
fragment_counts <- SummarizedExperiment(
assays = list(counts = counts_matrix),
rowRanges = peak_ranges
)2. Add GC Bias Correction
library(BSgenome.Hsapiens.UCSC.hg38) fragment_counts <- addGCBias(fragment_counts, genome = BSgenome.Hsapiens.UCSC.hg38)
3. Filter Low-Quality Peaks
# min_depth=1500: Minimum total reads per sample. Adjust based on library size.
# min_in_peaks=0.15: Minimum fraction of reads in peaks (FRiP). 0.15 = 15%.
fragment_counts <- filterSamples(fragment_counts, min_depth = 1500, min_in_peaks = 0.15)
# min_count=10: Require peaks with >=10 reads across samples.
# n_samples_frac=0.1: Peak must be detected in >=10% of samples.
fragment_counts <- filterPeaks(fragment_counts, non_overlapping = TRUE,
min_count = 10, n_samples_frac = 0.1)Get Motif Annotations
From JASPAR
library(JASPAR2020) library(TFBSTools) library(motifmatchr) # Get vertebrate motifs from JASPAR pfm <- getMatrixSet(JASPAR2020, opts = list(collection = 'CORE', tax_group = 'vertebrates')) # Match motifs to peaks # p.cutoff=5e-5: Motif match p-value threshold. Lower = more stringent. motif_ix <- matchMotifs(pfm, fragment_counts, genome = BSgenome.Hsapiens.UCSC.hg38, p.cutoff = 5e-5)
From CIS-BP or Custom PWMs
# Load custom motifs from file
library(universalmotif)
motifs <- read_meme('custom_motifs.meme')
pfm_list <- lapply(motifs, function(m) convert_motifs(m, class = 'TFBSTools-PFMatrix'))
motif_ix <- matchMotifs(pfm_list, fragment_counts, genome = BSgenome.Hsapiens.UCSC.hg38)Compute Deviations
# Compute chromVAR deviation scores dev <- computeDeviations(object = fragment_counts, annotations = motif_ix) # Extract deviation scores (z-scores) deviation_scores <- deviations(dev) # Extract variability across samples variability <- computeVariability(dev)
Interpreting Results
Deviation Scores
# Deviation z-scores: positive = more accessible than expected # Compare across samples dev_matrix <- deviations(dev) print(dim(dev_matrix)) # motifs x samples # Get top variable motifs var_df <- variability var_df <- var_df[order(-var_df$variability), ] head(var_df, 20)
Variability Interpretation
| Variability | Interpretation | |-------------|----------------| | > 2.0 | Highly variable across samples | | 1.0 - 2.0 | Moderately variable | | < 1.0 | Low variability |
Visualization
Deviation Heatmap
library(pheatmap)
# Get top variable motifs
# n_top=50: Number of top variable motifs to display.
n_top <- 50
top_motifs <- head(rownames(var_df), n_top)
top_dev <- deviation_scores[top_motifs, ]
# Add sample annotations
sample_info <- data.frame(
Condition = colData(fragment_counts)$condition,
row.names = colnames(top_dev)
)
pheatmap(top_dev, annotation_col = sample_info, scale = 'row',
clustering_method = 'ward.D2', show_rownames = TRUE)Variability Plot
plotVariability(variability, use_plotly = FALSE)
PCA of Deviation Scores
library(ggplot2)
# PCA on deviation scores
pca <- prcomp(t(deviation_scores), scale. = TRUE)
pca_df <- data.frame(PC1 = pca$x[,1], PC2 = pca$x[,2],
Condition = colData(fragment_counts)$condition)
ggplot(pca_df, aes(x = PC1, y = PC2, color = Condition)) +
geom_point(size = 3) +
theme_minimal() +
labs(title = 'PCA of chromVAR Deviations')Differential Motif Accessibility
**Goal:** Identify TF motifs with significantly different accessibility between experimental groups.
**Approach:** Fit a linear model (limma) to deviation z-scores across groups and extract significant motifs with empirical Bayes moderation.
Compare Two Groups
library(limma) # Get sample groups groups <- factor(colData(fragment_counts)$condition) # Design matrix design <- model.matrix(~ groups) # Fit linear model to deviation scores fit <- lmFit(deviation_scores, design) fit <- eBayes(fit) # Get differenti
The largest open-source medical AI skill library for OpenClaw.
Other skills on openclaw-medical-skills.
- /aav-vector-design-agent
<!--
Open skill - /adaptyv
Cloud laboratory platform for automated protein testing and validation. Use when designing proteins and needing experimental validation including binding assays, expression testing, thermostability measurements, enzyme activity assays, or protein sequence optimization. Also use
Open skill - /adhd-daily-planner
Time-blind friendly planning, executive function support, and daily structure for ADHD brains. Specializes in realistic time estimation, dopamine-aware task design, and building systems that
Open skill - /aeon
This skill should be used for time series machine learning tasks including classification, regression, clustering, forecasting, anomaly detection, segmentation, and similarity search. Use when working with temporal data, sequential patterns, or time-indexed observations
Open skill - /agent-browser
Browse the web for any task — research topics, read articles, interact with web apps, fill forms, take screenshots, extract data, and test web pages. Use whenever a browser would be useful, not just when the user explicitly asks.
Open skill - /agentd-drug-discovery
<!--
Open skill

