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/thesecondfox/skill/bio-multi-omics-integration-mofa-integrationnpx skills add thesecondfox/skill --skill bio-multi-omics-integration-mofa-integrationgit clone --depth 1 https://github.com/thesecondfox/skillWrote 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/thesecondfox/skill/bio-multi-omics-integration-mofa-integration)<a href="https://agentmods.dev/skills/thesecondfox/skill/bio-multi-omics-integration-mofa-integration"><img src="https://agentmods.dev/badge/skills/thesecondfox/skill/bio-multi-omics-integration-mofa-integration.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 5.1 | $0.00068 | $0.01900 |
| Opus 5 | $0.00034 | $0.00950 |
| Sonnet 5 | $0.00014 | $0.00380 |
| Haiku 4.5 | $0.00007 | $0.00190 |
Grade A, and why
bio-multi-omics-mofa-integration 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 2d 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 — 226 lines — stays where its author put it; the contents beside it link to each section on GitHub.
Version Compatibility
Reference examples tested with: scanpy 1.10+
Before using code patterns, verify installed versions match. If versions differ:
- R:
packageVersion('<pkg>')then?function_nameto verify parameters
If code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
MOFA2 Integration
"Find shared variation across my omics layers" → Discover latent factors that capture shared and modality-specific sources of biological variation in an unsupervised manner.
- R:
MOFA2::create_mofa()→prepare_mofa()→run_mofa() - Python:
mofapy2for training,muonfor downstream
Prepare Multi-Omics Data
Goal: Load and align multiple omics matrices into a consistent format for MOFA2 input.
Approach: Read each omics layer, intersect to common samples, transpose to features-by-samples orientation.
library(MOFA2)
library(MultiAssayExperiment)
# Load individual omics matrices (samples x features)
rna <- as.matrix(read.csv('rnaseq_matrix.csv', row.names = 1))
protein <- as.matrix(read.csv('proteomics_matrix.csv', row.names = 1))
methylation <- as.matrix(read.csv('methylation_matrix.csv', row.names = 1))
# Ensure consistent sample names across views
common_samples <- Reduce(intersect, list(rownames(rna), rownames(protein), rownames(methylation)))
rna <- rna[common_samples, ]
protein <- protein[common_samples, ]
methylation <- methylation[common_samples, ]
# Transpose to features x samples (MOFA format)
data_list <- list(
RNA = t(rna),
Protein = t(protein),
Methylation = t(methylation)
)
Create and Train MOFA Model
Goal: Configure and train a MOFA2 model to discover shared and view-specific latent factors.
Approach: Set model and training options, then run variational inference to learn factor decomposition.
# Create MOFA object
mofa <- create_mofa(data_list)
# View data overview
plot_data_overview(mofa)
# Set model options
model_opts <- get_default_model_options(mofa)
model_opts$num_factors <- 15 # Number of factors to learn
# Set training options
train_opts <- get_default_training_options(mofa)
train_opts$convergence_mode <- 'slow'
train_opts$seed <- 42
# Prepare and train
mofa <- prepare_mofa(mofa, model_options = model_opts, training_options = train_opts)
mofa <- run_mofa(mofa, outfile = 'mofa_model.hdf5')
What ships with it
1 file 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.
- 2d ago First seen · 226 lines · 68 tokens per session scan A d3f65d5e1310
bio-multi-omics-mofa-integration is a skill published in the GitHub repository thesecondfox/skill (3 stars, last pushed 5mo ago), licensed MIT. It adds 68 tokens to every session and 1,900 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 2026-09-03.
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