Macsr

MACSr

Workflows

Standard Workflow

library(MACSr)

# Call narrow peaks
cp1 <- callpeak(CHIP, CTRL, gsize = 5.2e7, store_bdg = TRUE,
                name = "run_callpeak_narrow0", outdir = tempdir(),
                cutoff_analysis = TRUE)

# Call broad peaks
cp2 <- callpeak(CHIP, CTRL, gsize = 5.2e7, store_bdg = TRUE,
                name = "run_callpeak_broad", outdir = tempdir(),
                broad = TRUE)

Input: ChIP-seq treatment and control alignment files (e.g., BED or BAM format). Output: A macsList object containing paths to called peaks (narrow or broad), summits, and bedGraph files.

When to Use

• Calling narrow or broad peaks from ChIP-seq alignment files using callpeak().
• Performing ATAC-seq chromatin accessibility peak calling using the Hidden Markov Model-based hmmratac().
• Comparing two signal tracks in bedGraph format using bdgcmp() or detecting differential peaks using bdgdiff().
• Predicting fragment size or d from alignment results using predictd().

When NOT to Use

• For initial sequence alignment or quality control of raw fastq files, use aligners like Rsubread or external tools like Bowtie2.
• For downstream peak annotation and motif discovery, use packages like ChIPseeker or motifStack.

Data Requirements

• Alignment files in BED, BAM, or other supported formats (can be gzipped).
• Effective genome size (gsize) corresponding to the organism of interest.

Key Parameters

• gsize (required): Effective genome size (e.g., 5.2e7 for a subset or standard values for organisms).
• store_bdg (FALSE): Logical indicating whether to save pileup and lambda signal tracks in bedGraph format.
• broad (FALSE): Logical indicating whether to call broad peaks instead of narrow peaks.
• cutoff_analysis (FALSE): Logical indicating whether to perform cutoff vs peak count analysis.
• name ("NA"): Character string prefix for output files.
• outdir ("."): Directory path where output files will be written.

Best Practices

• Always provide a control/input sample (CTRL) to increase peak-calling specificity and reduce false positives.
• Enable store_bdg = TRUE to generate signal tracks for downstream visualization in genome browsers.
• Inspect the execution log stored in the macsList object using cat(paste(cp1$log, collapse="\n")) to verify model building and fragment size prediction.

Common Pitfalls

• Using an incorrect effective genome size (gsize): This will lead to inaccurate p-value and q-value calculations. Ensure gsize matches your target organism.
• Forgetting that MACSr writes files directly to disk: Always specify a valid, writable outdir (e.g., tempdir()) to avoid permission issues.

Alternatives

• BayesPeak: For Bayesian analysis of ChIP-seq data.
• csaw: For window-based de novo detection of differentially bound regions.

Citations

• Zhang et al. (2008) "Model-based Analysis of ChIP-Seq (MACS)" (implied by the package description and vignette introduction).

References

• Homepage: bioconductor.org/packages/MACSr
• Vignette: https://bioconductor.org/packages/release/bioc/vignettes/MACSr/inst/doc/MACSr.html