Agent skill · Content & Marketing

bio-chipseq-allele-specific-binding

Detects allele-specific transcription factor or histone modification binding from heterozygous-variant ChIP-seq using WASP (reference-bias filter; mandatory upstream), RASQUAL (joint QTL + bias-corrected testing), BaalChIP (Bayesian beta-binomial with copy-number-aware overdispersion), and AlleleSeq (personalized diploid genome). Handles imprinted-locus awareness, X-inactivation artifacts, cancer copy-number imbalance, and integration with downstream caQTL / bQTL mapping. Use when identifying variants with allelic effects on TF binding, fine-mapping causal regulatory variants, validating deep-

BioTender-maxgithub.com/BioTender-maxGitHub ↗
claude-codeNOASSERTION
Install
npx skills add BioTender-max/awesome-bio-agent-skills --skill allele-specific-binding --agent claude-code

Same command for any agent — swap --agent for codex, cursor, copilot.

Facts
Files in the skill folder: 3
SKILL.md size: 14 KB
Bundled scripts: none
Path: skills/bioskills/allele-specific-binding/SKILL.md
Open the folder on GitHub →
Where it comes from
Stars: 135
Language: Python

Weekly change comes from our own snapshots, not the repository page — it measures attention, not adoption.

From the SKILL.md

## Version Compatibility Reference examples tested with: WASP 0.3.4+, RASQUAL 1.1+, BaalChIP 1.30+ (Bioconductor), AlleleSeq 2.0+, samtools 1.19+, bcftools 1.19+, GATK 4.5+, pysam 0.22+. # Allele-Specific Binding (ASB) **"Identify variants that affect transcription factor or histone modification binding in cis"** -> Compare ChIP-seq read counts at the reference and alternate alleles of heterozygous variants in a single sample. Differential read counts (ALT vs REF at hetSNPs in peaks) reveal allele-specific binding. - CLI (mandatory bias filter): WASP `mapping pipeline` to remove reference-allele mapping bias - CLI (joint association): RASQUAL with `--n-permutations` for cis-QTL + ASB - R (Bayesian beta-binomial): BaalChIP with copy-number-aware overdispersion - CLI (personalized genome): AlleleSeq with phased diploid genome - Statistical test: beta-binomial likelihood ratio or chi-squared on count tables ASB analysis has three universal pitfalls: reference-allele mapping bias (universal across short-read aligners), imprinted loci (constitutively allele-skewed by biology), and copy-number variation (changes effective allele dose). All three must be addressed or results are unreliabl

What's inside
Steps it walks through
  1. Version Compatibility
  2. Method Taxonomy
  3. Universal First Step: WASP Reference-Bias Filter
  4. Workflow: BaalChIP (Recommended for Cancer / Copy-Number-Imbalanced Samples)
  5. Workflow: RASQUAL (Joint cis-QTL + ASB)
  6. Workflow: AlleleSeq (Personalized Diploid Genome)
  7. Three Universal Pitfalls
  8. Pitfall 1: Imprinted Loci Are Constitutively Skewed
  9. Pitfall 2: X-Inactivation in Females
  10. Pitfall 3: Copy-Number Imbalance (Cancer Genomes)
  11. Per-Tool Failure Modes
  12. WASP -- Reference panel mismatch
  13. WASP -- Excessive read loss
  14. RASQUAL -- Convergence failure
Ships with 2 files
  • examples/baalchip_workflow.R
  • usage-guide.md
Commands it runs
WASP mapping pipeline
bowtie2 -x hg38 -1 R1.fq -2 R2.fq -S step1.sam
samtools view -bS step1.sam | samtools sort -o step1.bam
samtools index step1.bam
python /path/to/WASP/mapping/find_intersecting_snps.py \
step1.bam
bowtie2 -x hg38 -1 wasp_out/step1.remap.fq.gz -S step2.sam
python /path/to/WASP/mapping/filter_remapped_reads.py \
step1.to.remap.bam step2.bam step1.keep.bam
samtools sort -o step1.wasp.bam step1.keep.bam
More from awesome-bio-agent-skills
All skills →
About this skill
What does the bio-chipseq-allele-specific-binding skill do?

Detects allele-specific transcription factor or histone modification binding from heterozygous-variant ChIP-seq using WASP (reference-bias filter; mandatory upstream), RASQUAL (joint QTL + bias-corrected testing), BaalChIP (Bayesian beta-binomial with copy-number-aware overdispersion), and AlleleSeq (personalized diploid genome). Handles imprinted-locus awareness, X-inactivation artifacts, cancer copy-number imbalance, and integration with downstream caQTL / bQTL mapping. Use when identifying variants with allelic effects on TF binding, fine-mapping causal regulatory variants, validating deep-

How do I install it?

Run `npx skills add BioTender-max/awesome-bio-agent-skills --skill allele-specific-binding --agent claude-code` — it drops the skill into your project so the agent can pick it up. Swap the --agent value for codex, cursor or copilot if you use one of those.

Where does this skill come from?

From BioTender-max/awesome-bio-agent-skills, a repository with 135 stars. We read it straight from the repository tree rather than a submitted listing, so what you see here is what is actually published.

Is a popular skill a good skill?

Not necessarily. Stars measure attention, not adoption — a repository can trend for a week and be abandoned. That is why we show the weekly change from our own snapshots next to the total, instead of a single flattering number.

Keep going