Agent skill
bio-data-visualization-genome-tracks
Create genome browser-style visualizations showing multiple data tracks (coverage, peaks, genes) using pyGenomeTracks, Gviz, and IGV. Use when visualizing genomic data at specific loci with multiple aligned tracks.
Stars
163
Forks
31
Install this agent skill to your Project
npx add-skill https://github.com/majiayu000/claude-skill-registry/tree/main/skills/data/genome-tracks
SKILL.md
Genome Track Visualization
pyGenomeTracks (Python/CLI)
bash
# Create tracks configuration file
cat > tracks.ini << 'EOF'
[bigwig]
file = coverage.bw
title = Coverage
height = 4
color = #4DBBD5
min_value = 0
[spacer]
height = 0.5
[peaks]
file = peaks.bed
title = Peaks
color = #E64B35
height = 2
labels = false
[spacer]
height = 0.5
[genes]
file = genes.gtf
title = Genes
height = 5
fontsize = 10
style = flybase
color = #3C5488
[x-axis]
EOF
# Generate plot
pyGenomeTracks --tracks tracks.ini --region chr1:1000000-2000000 \
--outFileName tracks.png --dpi 150
pyGenomeTracks with Multiple Samples
ini
[sample1 coverage]
file = sample1.bw
title = Sample 1
height = 3
color = #4DBBD5
min_value = 0
max_value = auto
[sample2 coverage]
file = sample2.bw
title = Sample 2
height = 3
color = #E64B35
min_value = 0
max_value = auto
[sample1 peaks]
file = sample1_peaks.narrowPeak
title = Sample 1 Peaks
color = #4DBBD5
height = 1
file_type = narrowPeak
[sample2 peaks]
file = sample2_peaks.narrowPeak
title = Sample 2 Peaks
color = #E64B35
height = 1
file_type = narrowPeak
pyGenomeTracks Programmatic
python
import pygenometracks.tracks as pygtk
tracks = pygtk.PlotTracks('tracks.ini', fig_width=40, dpi=150)
tracks.plot('output.png', 'chr1', 1000000, 2000000)
Gviz (R)
r
library(Gviz)
library(GenomicRanges)
# Genome axis
gtrack <- GenomeAxisTrack()
# Ideogram
itrack <- IdeogramTrack(genome = 'hg38', chromosome = 'chr1')
# Gene model
library(TxDb.Hsapiens.UCSC.hg38.knownGene)
txdb <- TxDb.Hsapiens.UCSC.hg38.knownGene
grtrack <- GeneRegionTrack(txdb, genome = 'hg38', chromosome = 'chr1',
name = 'Genes', transcriptAnnotation = 'symbol')
# Data track from BigWig
dtrack <- DataTrack(range = 'coverage.bw', genome = 'hg38', chromosome = 'chr1',
name = 'Coverage', type = 'histogram', col.histogram = '#4DBBD5')
# Annotation track from BED
atrack <- AnnotationTrack(range = 'peaks.bed', genome = 'hg38', chromosome = 'chr1',
name = 'Peaks', fill = '#E64B35')
# Plot tracks
plotTracks(list(itrack, gtrack, dtrack, atrack, grtrack),
from = 1000000, to = 2000000, sizes = c(1, 1, 3, 1, 3))
Gviz with Multiple Samples
r
# Create overlay data track
dtrack1 <- DataTrack(range = 'sample1.bw', name = 'Sample1', col = '#4DBBD5')
dtrack2 <- DataTrack(range = 'sample2.bw', name = 'Sample2', col = '#E64B35')
overlay <- OverlayTrack(trackList = list(dtrack1, dtrack2))
plotTracks(list(gtrack, overlay, grtrack), from = 1000000, to = 2000000,
type = 'histogram', legend = TRUE)
Gviz Customization
r
# Highlight regions
ht <- HighlightTrack(trackList = list(dtrack, atrack),
start = c(1200000, 1500000),
end = c(1300000, 1600000),
chromosome = 'chr1')
# Custom display parameters
displayPars(dtrack) <- list(
background.title = '#3C5488',
fontcolor.title = 'white',
col.axis = 'black',
ylim = c(0, 100)
)
plotTracks(list(gtrack, ht, grtrack), from = 1000000, to = 2000000)
IGV.js (Web)
html
<!DOCTYPE html>
<html>
<head>
<script src="https://cdn.jsdelivr.net/npm/igv@3.0.0/dist/igv.min.js"></script>
</head>
<body>
<div id="igv-div"></div>
<script>
var options = {
genome: "hg38",
locus: "chr1:1,000,000-2,000,000",
tracks: [
{
name: "Coverage",
url: "coverage.bw",
type: "wig",
color: "#4DBBD5"
},
{
name: "Peaks",
url: "peaks.bed",
type: "annotation",
color: "#E64B35"
}
]
};
igv.createBrowser(document.getElementById('igv-div'), options);
</script>
</body>
</html>
Create BigWig from BAM
bash
# Using deepTools
bamCoverage -b sample.bam -o coverage.bw \
--binSize 10 --normalizeUsing RPKM --effectiveGenomeSize 2913022398
# Using bedtools + wigToBigWig
bedtools genomecov -bg -ibam sample.bam > coverage.bedGraph
sort -k1,1 -k2,2n coverage.bedGraph > coverage.sorted.bedGraph
bedGraphToBigWig coverage.sorted.bedGraph chrom.sizes coverage.bw
Multi-Region Plot
bash
# pyGenomeTracks with BED regions
pyGenomeTracks --tracks tracks.ini --BED regions.bed \
--outFileName multi_region.pdf --dpi 150
r
# Gviz with multiple regions
regions <- GRanges(seqnames = 'chr1', ranges = IRanges(start = c(1e6, 2e6), end = c(1.5e6, 2.5e6)))
pdf('multi_region.pdf', width = 10, height = 8)
for (i in seq_along(regions)) {
plotTracks(track_list, from = start(regions[i]), to = end(regions[i]))
}
dev.off()
Related Skills
- genome-intervals/bigwig-tracks - BigWig file handling
- chip-seq/chipseq-visualization - ChIP-specific tracks
- hi-c-analysis/hic-visualization - Hi-C contact maps
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