Getting it into your agent
One page per mod, every tool's command on it. A separate URL per tool would split the same page into five that compete with each other.
npx agentmods add skills/mannlabs/proteomics-agent-skills/normalizing_proteomics_datanpx skills add MannLabs/proteomics-agent-skills --skill normalizing_proteomics_datagit clone --depth 1 https://github.com/MannLabs/proteomics-agent-skillsWrote 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/mannlabs/proteomics-agent-skills/normalizing_proteomics_data)<a href="https://agentmods.dev/skills/mannlabs/proteomics-agent-skills/normalizing_proteomics_data"><img src="https://agentmods.dev/badge/skills/mannlabs/proteomics-agent-skills/normalizing_proteomics_data.svg" alt="Measured on agentmods" 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 | $0.00054 | $0.00743 |
| Opus 5 | $0.00027 | $0.00371 |
| Sonnet 5 | $0.00011 | $0.00149 |
| Haiku 4.5 | $0.00005 | $0.00074 |
Grade A, and why
normalizing-proteomics-data 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 4d 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.
How it starts
The opening of the file, as written. The whole thing — 70 lines — stays where its author put it; the contents beside it link to each section on GitHub.
Normalizing Proteomics Data
Normalization makes samples comparable by aligning their overall intensity distributions. It serves three main goals:
- Aligning intensities across samples, which removes technical variation caused by differences in sample loading amounts or instrument behavior.
- Preserving feature ranks within each sample, so the relative ordering of features is not distorted.
- Stabilizing variance (i.e., addressing heteroscedasticity), which most downstream methods require because they assume homoscedastic noise.
After normalization, a feature's intensity should reflect its relative biological abundance within a sample and remain comparable across samples.
Common normalization methods include:
| Priority | Method | Input scale | | --- | --- | --- | --- | | 1 | Total sum normalization | Simple offset correction; robust baseline | Linear-scale intensities | | 2 | Quantile Normalization | Distributions should be identical across samples | Log-transformed intensities | | 3 | Variance Stabilizing Normalization (VSN) | Need variance stabilization of low-abundant features; performs well in differential expression benchmarks | Linear-scale intensities | | 4 | LOESS/RLR | Suspect intensity-dependent bias (non-linear or linear) | Log-transformed intensities |
Recommendation: Start with log2 only. If PCA shows intensity-driven structure, try total sum normalization, then VSN.
Checklist
Copy this checklist and track progress:
Analysis step progress:
- [ ] Verify log2 transformation
- [ ] Assess Normalization Need
- [ ] Data dependent: Select Additional Normalization
- [ ] Evaluate Normalization Effect
If Successful: Proceed to "Batch correction"
If Unsuccessful: Return to Step 3 (Select normalization method 2, 3, etc.)
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.
- 4d ago First seen · 70 lines · 54 tokens per session scan A 74cf60e8a8e7
normalizing-proteomics-data is a skill published in the GitHub repository MannLabs/proteomics-agent-skills (14 stars, last pushed 1mo ago), licensed Apache-2.0. It adds 54 tokens to every session and 743 once invoked, about $0.0003 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 2026-08-30.
Other skills, from other repositories
proteomics-de
Load when computing two-group differential protein abundance (group2 vs group1, log2FC + p-value + BH-adjusted FDR) via Welch t-test, equal-variance t-test, or Mann-Whitney on a wide protein × sample CSV. Skip when you need multi-condition DE (run pairwise contrasts manually); label-based TMT linear-mixed models.
proteomics-ptm
Load when summarising PTM sites (phosphorylation, acetylation, ubiquitination, etc.) from a per-site CSV — site-class assignment (Olsen et al. Class I/II/III by localizationprobability), per-PTM-type counts, amino-acid distribution, sites-per-protein. Skip when raw spectra are the input; you only need protein-level…
proteomics-quantification
Load when computing per-protein abundance from a peptide / PSM table via LFQ (intensity summation), iBAQ (intensity / tryptic peptide count), or spectral counting (PSMs per protein). Skip when the input is already protein-level (use proteomics-ms-qc); label-based TMT / iTRAQ workflows (search upstream first).
proteomics-structural
Load when summarising cross-linking MS (XL-MS) results — intra/inter-protein link split, optional FDR filtering, distance-constraint validation against a per-crosslinker (DSS / BS3 / EDC / DSSO / DSBU) max distance. Skip when raw spectra are the input (run XlinkX / pLink / xiSEARCH first); no XL-MS experiment was…
proteomics-data-import
Load when ingesting a MaxQuant proteinGroups.txt, FragPipe combinedprotein.tsv, DIA-NN report, or generic CSV / TSV protein-quantification table — normalises columns to a standard schema, emits tables/proteins.csv. Skip when raw spectra are the input (run the search engine first); the file is already OmicsClaw schema.
proteomics-enrichment
Load when running over-representation analysis (ORA) on a list of proteins via Fisher's exact test against a built-in 8-pathway DEMO dictionary, with BH-FDR correction. Skip when needing a real pathway database (this skill is demo-only) (use bulkrna-enrichment); rank-based GSEA.