install
source · Clone the upstream repo
git clone https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills
Claude Code · Install into ~/.claude/skills/
T=$(mktemp -d) && git clone --depth=1 https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills "$T" && mkdir -p ~/.claude/skills && cp -r "$T/skills/bio-epitranscriptomics-m6a-peak-calling" ~/.claude/skills/freedomintelligence-openclaw-medical-skills-bio-epitranscriptomics-m6a-peak-call && rm -rf "$T"
OpenClaw · Install into ~/.openclaw/skills/
T=$(mktemp -d) && git clone --depth=1 https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills "$T" && mkdir -p ~/.openclaw/skills && cp -r "$T/skills/bio-epitranscriptomics-m6a-peak-calling" ~/.openclaw/skills/freedomintelligence-openclaw-medical-skills-bio-epitranscriptomics-m6a-peak-call && rm -rf "$T"
manifest:
skills/bio-epitranscriptomics-m6a-peak-calling/SKILL.mdsource content
<!--
# COPYRIGHT NOTICE
# This file is part of the "Universal Biomedical Skills" project.
# Copyright (c) 2026 MD BABU MIA, PhD <md.babu.mia@mssm.edu>
# All Rights Reserved.
#
# This code is proprietary and confidential.
# Unauthorized copying of this file, via any medium is strictly prohibited.
#
# Provenance: Authenticated by MD BABU MIA
-->
name: bio-epitranscriptomics-m6a-peak-calling description: Call m6A peaks from MeRIP-seq IP vs input comparisons. Use when identifying m6A modification sites from methylated RNA immunoprecipitation data. tool_type: mixed primary_tool: exomePeak2 measurable_outcome: Execute skill workflow successfully with valid output within 15 minutes. allowed-tools:
- read_file
- run_shell_command
m6A Peak Calling
exomePeak2 (Recommended)
library(exomePeak2) # Peak calling with biological replicates result <- exomePeak2( bam_ip = c('IP_rep1.bam', 'IP_rep2.bam'), bam_input = c('Input_rep1.bam', 'Input_rep2.bam'), gff = 'genes.gtf', genome = 'hg38', paired_end = TRUE ) # Export peaks exportResults(result, format = 'BED')
MACS3 Alternative
# Call peaks treating input as control macs3 callpeak \ -t IP_rep1.bam IP_rep2.bam \ -c Input_rep1.bam Input_rep2.bam \ -f BAMPE \ -g hs \ -n m6a_peaks \ --nomodel \ --extsize 150 \ -q 0.05
MeTPeak
library(MeTPeak) # GTF-aware peak calling metpeak( IP_BAM = c('IP_rep1.bam', 'IP_rep2.bam'), INPUT_BAM = c('Input_rep1.bam', 'Input_rep2.bam'), GENE_ANNO_GTF = 'genes.gtf', OUTPUT_DIR = 'metpeak_output' )
Peak Filtering
# Filter by fold enrichment and q-value # FC > 2, q < 0.05 typical thresholds awk '$7 > 2 && $9 < 0.05' peaks.xls > filtered_peaks.bed
Related Skills
- merip-preprocessing - Prepare data for peak calling
- m6a-differential - Compare peaks between conditions
- chip-seq/peak-calling - Similar concepts