bio-microbiome-functional-prediction — independently scanned and version-tracked by SaferSkills.
SaferSkills independently audited bio-microbiome-functional-prediction (Agent Skill) and scored it 100/100 (green). The audit ran 55 deterministic rules across Security, Supply Chain, Maintenance, Transparency, and Community; it found 0 high-severity and 0 lower-severity findings. The full rule-by-rule trace and per-finding evidence are below. Free, methodology-open.
Findings & checks · 0 flagged
Every scanned point with the score it earned and what moved between them.
First recorded scan — no prior version to compare against.
The primary manifest — the file an agent reads to learn what this artifact does.
Reference examples tested with: Biostrings 2.70+, ggplot2 3.5+, pandas 2.2+, phyloseq 1.46+, scanpy 1.10+
Before using code patterns, verify installed versions match. If versions differ:
pip show <package> then help(module.function) to check signaturespackageVersion('<pkg>') then ?function_name to verify parameters<tool> --version then <tool> --help to confirm flagsIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Predict functional pathways from my 16S data" → Infer metagenome functional content from marker gene (16S/ITS) ASV tables using phylogenetic placement and gene content prediction.
picrust2_pipeline.py -s seqs.fna -i table.biom -o output/library(phyloseq)
library(Biostrings)
ps <- readRDS('phyloseq_object.rds')
# Export ASV table (samples as columns)
otu <- as.data.frame(otu_table(ps))
if (!taxa_are_rows(ps)) otu <- t(otu)
write.table(otu, 'asv_table.tsv', sep = '\t', quote = FALSE)
# Export ASV sequences as FASTA
seqs <- refseq(ps) # Or extract from ASV names if stored there
writeXStringSet(seqs, 'asv_seqs.fasta')# Full pipeline (place sequences, predict functions, metagenome inference)
picrust2_pipeline.py \
-s asv_seqs.fasta \
-i asv_table.tsv \
-o picrust2_output \
-p 4 \
--stratified \
--per_sequence_contrib
# Output files:
# - pathway_abundance.tsv (MetaCyc pathways)
# - KO_metagenome_out/pred_metagenome_unstrat.tsv (KEGG orthologs)
# - EC_metagenome_out/pred_metagenome_unstrat.tsv (EC numbers)Goal: Predict functional metagenome content from 16S ASVs using the full PICRUSt2 pipeline with explicit control over each step.
Approach: Place ASV sequences into a reference tree, predict gene content via hidden-state prediction, infer per-sample metagenome abundances, and reconstruct MetaCyc pathways.
# 1. Place sequences in reference tree
place_seqs.py -s asv_seqs.fasta -o placed_seqs.tre -p 4
# 2. Hidden state prediction (gene content)
hsp.py -i 16S -t placed_seqs.tre -o marker_nsti_predicted.tsv -m pic -n
# 3. Predict gene families (KO)
hsp.py -i KO -t placed_seqs.tre -o KO_predicted.tsv -m pic
# 4. Metagenome inference
metagenome_pipeline.py \
-i asv_table.tsv \
-m marker_nsti_predicted.tsv \
-f KO_predicted.tsv \
-o KO_metagenome_out \
--strat_out
# 5. Pathway inference
pathway_pipeline.py \
-i KO_metagenome_out/pred_metagenome_contrib.tsv \
-o pathway_output \
-p 4import pandas as pd
# NSTI = Nearest Sequenced Taxon Index
# Lower = more reliable prediction (< 2 is acceptable)
nsti = pd.read_csv('marker_nsti_predicted.tsv', sep='\t')
print(f'Mean NSTI: {nsti["metadata_NSTI"].mean():.3f}')
print(f'ASVs with NSTI > 2: {(nsti["metadata_NSTI"] > 2).sum()}')library(ggplot2)
pathways <- read.delim('picrust2_output/pathways_out/path_abun_unstrat.tsv', row.names = 1)
metadata <- read.csv('sample_metadata.csv', row.names = 1)
# Normalize to relative abundance
pathways_rel <- sweep(pathways, 2, colSums(pathways), '/')
# Differential pathway analysis (use ALDEx2 or similar)
library(ALDEx2)
groups <- metadata[colnames(pathways), 'Group']
pathway_aldex <- aldex(as.data.frame(t(pathways)), groups, mc.samples = 128)# Map pathway IDs to names
add_descriptions.py \
-i pathway_abundance.tsv \
-m METACYC \
-o pathway_abundance_described.tsv# Analyze KEGG modules instead of individual KOs
ko_table <- read.delim('KO_metagenome_out/pred_metagenome_unstrat.tsv', row.names = 1)
# Use KEGGREST for module mapping
library(KEGGREST)
modules <- keggLink('module', 'ko')~30 seconds. Free. No account. Every finding cites a rule and a line of evidence.