Getting it into your agent
It runs from inside its repository, so the clone comes first — what it calls does not travel with the file alone.
git clone --depth 1 https://github.com/GPTomics/bioSkillsnpx agentmods add skills/gptomics/bioskills/binding-site-annotationWrote this? Show the measurements
A badge with what this costs and how it scanned, read live from this page, so it follows the numbers instead of freezing them. Markdown for a README, HTML for a documentation site or a project page.
[](https://agentmods.dev/skills/gptomics/bioskills/binding-site-annotation)<a href="https://agentmods.dev/skills/gptomics/bioskills/binding-site-annotation"><img src="https://agentmods.dev/badge/skills/gptomics/bioskills/binding-site-annotation/github.svg" alt="Measured on agentmods" height="20"></a>Or the 80×15 button, for a site that already has a row of RSS and ATOM ones. Only the verdict fits; the numbers stay here.
<a href="https://agentmods.dev/skills/gptomics/bioskills/binding-site-annotation"><img src="https://agentmods.dev/badge/skills/gptomics/bioskills/binding-site-annotation.svg" alt="Reviewed on agentmods" width="80" height="20"></a>What it costs to keep this loaded
Counted locally with the o200k_base tokenizer, which is exact for GPT models; Claude uses its own tokenizer and its counts differ. Treat this as one consistent yardstick across the catalogue rather than a bill. Prices are per million input tokens.
| Model | Per session | Once invoked |
|---|---|---|
| Fable 5.1 | $0.00142 | $0.05932 |
| Opus 5 | $0.00071 | $0.02966 |
| Sonnet 5 | $0.00028 | $0.01186 |
| Haiku 4.5 | $0.00014 | $0.00593 |
Grade A, and why
bio-clip-seq-binding-site-annotation scanned grade A with 0 findings against 26 rules in 11 categories — prompt injection, anti-refusal, data exfiltration, privilege escalation, supply chain, agent snooping, system-prompt leakage, SSRF and excessive agency — measured 7d ago.
A static scan of the body, not an audit. Every finding is printed with the line that produced it so you can judge whether it matters here. A mod is markdown that instructs an agent; that is exactly why what it instructs is worth reading.
Nothing flagged
None of the 26 patterns this scan looks for appear in this file: no shell pipes, no recursive deletes, no credential paths, no hidden text, no instruction-override or anti-refusal phrasing, no agent-config snooping. That is not a guarantee, it is the absence of the things that are checkable.
Copies of this mod
1 near-identical copy found in the catalogue:
- bio-clip-seq-binding-site-annotation — 95% identical, 12 lines differ
How it starts
The opening of the file, as written. The whole thing — 329 lines — stays where its author put it; the contents beside it link to each section on GitHub.
Version Compatibility
Reference examples tested with: ChIPseeker 1.40+, RCAS 1.30+, GenomicFeatures 1.56+, GenomicRanges 1.56+, rbp-maps (Yeo github), bedtools 2.31+, pybedtools 0.10+, pyranges 0.0.129+.
Before using code patterns, verify installed versions match. If versions differ:
- R:
packageVersion('<pkg>')then?function_nameto verify parameters - Python:
pip show <package>thenhelp(module.function)to check signatures - CLI:
<tool> --versionthen<tool> --helpto confirm flags
If code throws unexpected errors, introspect the installed package and adapt the example to match the actual API rather than retrying. ChIPseeker 1.40+ changed the priority defaults; verify the priority vector before pipelining.
Binding Site Annotation
"Annotate where in transcripts my RBP binds" -> Map CLIP peaks or single-nucleotide crosslink sites to RNA features and report the per-feature distribution. The interpretation is RBP-class-specific: splicing factors (PTBP1, U2AF2, RBFOX) bind intron-exon junctions; mRNA-stability regulators (HuR, PUM2) bind 3' UTRs; translation factors (EIF3J, RPS19) bind 5' UTRs and CDS; and small-ncRNA-binding RBPs (NSUN2 tRNAs, LARP7 7SK, TROVE2 Y-RNAs) bind specific non-coding transcripts. A correct annotation pipeline (a) resolves overlapping features by priority, (b) preserves transcript-isoform context, (c) generates metagene distributions, and (d) flags repeat-element overlap separately.
- R (peak-level, fast):
ChIPseeker::annotatePeak(peaks, TxDb=txdb, level='gene', tssRegion=c(-100,100))thenplotAnnoPie(anno) - R (transcript-level with RNA-specific regions): RCAS
runReport(queryRegions=peaks, gffData=gencode_gtf, genomeVersion='hg38') - CLI (regions only):
bedtools intersect -s -wa -wb -a peaks.bed -b features.bed(manual hierarchy) - R (splicing-regulatory map for splice factors): RBP-Maps (
yeolab/rbp-maps) generates the 1400 nt vectorized cassette-exon map used in Yeo lab ENCODE papers - CLI (metagene aggregation):
deepTools computeMatrixor RSeQCgeneBody_coverage.pyfor read profiles
What ships with it
2 files beside SKILL.md in the same directory: the scripts, references and assets a skill reads on demand. Not counted in the per-session cost; read them before you install if any of them is executable.
What this file has done since we first saw it
Hashed on every crawl. A supply-chain change to an agent config is a question of when, not whether, so the history is kept rather than the latest state alone.
- 7d ago First seen · 329 lines · 142 tokens per session scan A 1d883906734f
bio-clip-seq-binding-site-annotation is a skill published in the GitHub repository GPTomics/bioSkills (1,199 stars, last pushed 26d ago), licensed MIT. It adds 142 tokens to every session and 5,932 once invoked, about $0.0007 per session on Opus 5. A static security scan graded it A with 0 findings. No closer match exists in the catalogue, so it is treated as the original; first seen 2026-09-03.
Other skills, from other repositories
instrument-data-to-allotrope
Convert laboratory instrument output files (PDF, CSV, Excel, TXT) to Allotrope Simple Model (ASM) JSON format or flattened 2D CSV. Use this skill when scientists need to standardize instrument data for LIMS systems, data lakes, or downstream analysis. Supports auto-detection of instrument types. Outputs include full…
matlab
Build, review, migrate, and safely plan MATLAB or GNU Octave numerical workflows, including arrays, tabular/time data, tests, projects, graphics, MAT files, and explicit Python interoperability.
exploratory-data-analysis
Perform bounded, local exploratory analysis of explicitly supported scientific files. Use for redacted CSV/TSV/JSON profiles; optional NumPy, HDF5, FASTA/FASTQ, and basic image metadata inspection; missingness/leakage audits; outlier and transformation sensitivity; and rigorous EDA report scaffolds. Other domain…
phylogenetics
Build and analyze phylogenetic trees using MAFFT (multiple alignment), IQ-TREE 2 (maximum likelihood), and FastTree (fast NJ/ML). Visualize with ETE3 or FigTree. For evolutionary analysis, microbial genomics, viral phylodynamics, protein family analysis, and molecular clock studies.
research-engineer
An uncompromising Academic Research Engineer. Operates with absolute scientific rigor, objective criticism, and zero flair. Focuses on theoretical correctness, formal verification, and optimal implementation across any required technology.
mapping-to-snomed
Maps clinical concept spans extracted by OpenMed to SNOMED CT concepts through a USER-SUPPLIED terminology server (the user's own Ontoserver, Snowstorm, or UMLS/UTS), never a bundled vocabulary. Use when the user wants to code findings, disorders, procedures, body structures, or substances to SNOMED CT, run an ECL…