multi-omics-pipeline

name	multi-omics-pipeline
description	Pipeline skill for multi-omics data processing and integration. Use when the user asks to map gene IDs between HGNC Ensembl and UniProt, convert between omic data formats, run batch correction with ComBat or ComBat-seq, perform GSEA or over-representation analysis on multi-omic results, run consensus clustering on integrated data, execute MOFA2 in R or mofapy2 in Python, build a multi-omics ETL pipeline, harmonize feature identifiers across omics layers, or run clusterProfiler enrichment. Triggers include "map Ensembl to HGNC", "ID mapping omics", "ComBat code", "run MOFA2", "mofapy2", "GSEA Python", "fgsea R", "consensus clustering", "multi-omics pipeline", "gseapy", "biomaRt", "clusterProfiler", "mixOmics DIABLO".
usage	Invoke to generate executable code for multi-omics ID mapping, batch correction, factor analysis, enrichment, and consensus clustering.
version	1.0.0
validated_against	{"date":"2025-01-15T00:00:00.000Z","packages":{"mofa2":"1.12","combat":"0.3.4","gseapy":"1.1"}}
tags	["skill","category:pipeline","multi-omics","etl","hcls"]

Multi-Omics Pipeline — Pipeline Skill

Overview

Provide deterministic, copy-paste-ready code for multi-omics data processing tasks: ID mapping, batch correction, integration via MOFA2/mofapy2, enrichment analysis, and consensus clustering.

Usage

• Map gene identifiers across HGNC, Ensembl, and UniProt systems
• Run batch correction (ComBat/ComBat-seq) and multi-omic factor analysis (MOFA2/mofapy2)
• Perform GSEA enrichment and consensus clustering on integrated data

Core Concepts

---

Response Format

• Lead with the command or code the user needs — explain after
• Structure as: confirm inputs → working code → key parameters explained → gotchas
• One complete working example per task; do not show every alternative
• Keep code comments minimal and functional (what, not why-it-exists)
• Target: 50-100 lines of code with brief surrounding explanation

1. ID Mapping

1a. Python — HGNC Symbol ↔ Ensembl ↔ UniProt

import pandas as pd
import mygene

mg = mygene.MyGeneInfo()

# Input: list of HGNC symbols
genes = ["TP53", "BRCA1", "EGFR", "KRAS"]

# Query multiple ID types at once
result = mg.querymany(
    genes,
    scopes="symbol",
    fields="ensembl.gene,uniprot.Swiss-Prot",
    species="human",
    returnall=True,
)

df = pd.DataFrame(result["out"])
# Handle many-to-many: explode nested Ensembl IDs
df_ensembl = df.explode("ensembl")
df_ensembl["ensembl_id"] = df_ensembl["ensembl"].apply(
    lambda x: x["gene"] if isinstance(x, dict) else None
)
print(df_ensembl[["query", "ensembl_id"]].dropna())

1b. R — biomaRt

library(biomaRt)

ensembl <- useEnsembl(biomart = "genes", dataset = "hsapiens_gene_ensembl")

# Map HGNC symbols to Ensembl gene IDs and UniProt accessions
mapping <- getBM(
  attributes = c("hgnc_symbol", "ensembl_gene_id", "uniprotswissprot"),
  filters = "hgnc_symbol",
  values = c("TP53", "BRCA1", "EGFR", "KRAS"),
  mart = ensembl
)

# Remove rows with empty UniProt
mapping <- mapping[mapping$uniprotswissprot != "", ]
print(mapping)

ID Mapping Parameter Table

Parameter	Python (mygene)	R (biomaRt)
Input ID type	scopes="symbol"	filters = "hgnc_symbol"
Output ID types	fields="ensembl.gene,uniprot.Swiss-Prot"	attributes = c("ensembl_gene_id", "uniprotswissprot")
Species filter	species="human"	dataset = "hsapiens_gene_ensembl"
Many-to-many handling	Explode nested lists	Multiple rows returned automatically

---

2. Batch Correction

2a. Python — ComBat (pycombat)

from combat.pycombat import pycombat
import pandas as pd
import numpy as np

# expression_df: genes (rows) x samples (columns), log-transformed
# batch: list of batch labels, same order as columns
# covariates: DataFrame with biological covariates to protect

expression_df = pd.read_csv("expression_matrix.csv", index_col=0)
batch = [1, 1, 1, 2, 2, 2, 3, 3, 3]  # batch labels per sample

# Protect biological covariate (e.g., disease status)
covar_df = pd.DataFrame({"disease": [0, 0, 1, 0, 1, 1, 0, 1, 1]})

corrected = pycombat(
    expression_df,
    batch,
    mod=covar_df,       # biological covariates to protect
    par_prior=True,     # parametric adjustment (default)
)

2b. R — ComBat / ComBat-seq

library(sva)

# For continuous data (log-transformed expression, protein intensity)
# expr_mat: genes x samples matrix
# batch: vector of batch labels
# mod: model matrix with biological covariates to protect

mod <- model.matrix(~ disease_status, data = sample_info)

corrected <- ComBat(
  dat = expr_mat,
  batch = sample_info$batch,
  mod = mod,
  par.prior = TRUE  # parametric
)

# For count data (RNA-seq raw counts) — use ComBat-seq
corrected_counts <- ComBat_seq(
  counts = count_mat,
  batch = sample_info$batch,
  group = sample_info$disease_status  # biological variable to protect
)

Batch Correction Parameter Table

Parameter	ComBat (continuous)	ComBat-seq (counts)
Input	Log-transformed matrix	Raw count matrix (integers)
Parametric prior	par.prior = TRUE (default)	Not applicable
Biological covariate	mod (model matrix)	group (vector)
Output	Corrected continuous matrix	Corrected count matrix
When to use	Proteomics, methylation M-values, log-expression	RNA-seq raw counts

---

3. MOFA2 / mofapy2 Integration

3a. R — MOFA2

library(MOFA2)

# Prepare data: list of matrices, one per omic layer
# Each matrix: features x samples
data_list <- list(
  transcriptomics = expr_mat,   # genes x samples
  proteomics = prot_mat,        # proteins x samples
  methylation = meth_mat        # CpG sites x samples
)

# Create MOFA object
mofa <- create_mofa(data_list)

# Set data options
data_opts <- get_default_data_options(mofa)

# Set model options
model_opts <- get_default_model_options(mofa)
model_opts$num_factors <- 20  # start with 20; inactive factors pruned automatically

# Set training options
train_opts <- get_default_training_options(mofa)
train_opts$convergence_mode <- "slow"  # more iterations for better convergence
train_opts$seed <- 42

# Prepare and run
mofa <- prepare_mofa(
  mofa,
  data_options = data_opts,
  model_options  model_opts
  training_options  train_opts


mofa  run_mofamofa outfile  


plot_variance_explainedmofa


weights  get_weightsmofa views   factors   as.data.frame  
top_genes  weightsorderweightsvalue decreasing    

3b. Python — mofapy2

from mofapy2.run.entry_point import entry_point
import numpy as np

# Prepare data: list of numpy arrays [views][groups]
# Each array: samples x features
data = [
    [expr_array],   # view 0: transcriptomics, group 0
    [prot_array],   # view 1: proteomics, group 0
    [meth_array],   # view 2: methylation, group 0
]

ent = entry_point()
ent.set_data_options(scale_groups=False, scale_views=True)
ent.set_data_matrix(data, views_names=["transcriptomics", "proteomics", "methylation"])

ent.set_model_options(factors=20, spikeslab_weights=True, ard_factors=True)
ent.set_train_options(iter=1000, convergence_mode="slow", seed=42)

ent.build()
ent.run()
ent.save("mofa_model.hdf5")

MOFA Parameter Table

Parameter	Default	Guidance
num_factors / factors	10	Set 15–25 for exploratory analysis; inactive factors auto-pruned
convergence_mode	"fast"	Use "slow" for final analysis; "fast" for exploration
scale_views	TRUE / True	MUST be True to equalize variance across views
spikeslab_weights	TRUE / True	Enables sparse feature selection per factor
ard_factors	TRUE / True	Automatic relevance determination; prunes inactive factors
seed	None	ALWAYS set for reproducibility

---

4. GSEA Enrichment

4a. Python — gseapy

import gseapy as gp
import pandas as pd

# ranked_genes: DataFrame with columns ["gene", "rank_metric"]
# rank_metric can be: log2FC, -log10(p) * sign(FC), or MOFA weight
ranked_genes = pd.read_csv("ranked_genes.csv")

# Pre-ranked GSEA against MSigDB Hallmark gene sets
result = gp.prerank(
    rnk=ranked_genes,
    gene_sets="MSigDB_Hallmark_2020",
    min_size=15,
    max_size=500,
    permutation_num=1000,
    seed=42,
    outdir="gsea_results",
)

# Filter significant results
sig = result.res2d[result.res2d["FDR q-val"] < 0.05]
print(sig[["Term", "NES", "FDR q-val"]].sort_values("NES", ascending=False))

4b. R — fgsea with clusterProfiler

library(fgsea)
library(msigdbr)

# Get Hallmark gene sets for human
hallmark <- msigdbr(species = "Homo sapiens", category = "H")
pathways <- split(hallmark$gene_symbol, hallmark$gs_name)

# ranked_genes: named numeric vector (names = gene symbols, values = rank metric)
ranked_genes <- setNames(de_results$log2FoldChange, de_results$gene_symbol)
ranked_genes <- sort(ranked_genes, decreasing = TRUE)

# Run fgsea
fgsea_res <- fgsea(
  pathways = pathways,
  stats = ranked_genes,
  minSize = 15,
  maxSize = 500,
  nPermSimple = 10000
)

# Filter and sort
sig_pathways <- fgsea_res[fgsea_res$padj   
sig_pathways  sig_pathwaysordersig_pathwaysNES decreasing   
printsig_pathways   

Enrichment Parameter Table

Parameter	gseapy (Python)	fgsea (R)
Gene set source	"MSigDB_Hallmark_2020" or GMT file	msigdbr() + split()
Min gene set size	min_size=15	minSize = 15
Max gene set size	max_size=500	maxSize = 500
Permutations	permutation_num=1000	nPermSimple = 10000
Significance threshold	FDR q-val < 0.05	padj < 0.05
Rank metric	log2FC, signed -log10(p), or MOFA weight	Same

---

5. Consensus Clustering

Python — scikit-learn based consensus

import numpy as np
from sklearn.cluster import KMeans
from sklearn.metrics import silhouette_score

def consensus_clustering(data, k_range=range(2, 9), n_iterations=100, seed=42):
    """Run consensus clustering over a range of k values.
    data: samples x features array. Returns dict mapping k to results.
    """
    rng = np.random.default_rng(seed)
    n_samples = data.shape[0]
    results = {}

    for k in k_range:
        co_occurrence = np.zeros((n_samples, n_samples))
        co_sampled = np.zeros((n_samples, n_samples))

        for _ in range(n_iterations):
            # Subsample 80% of samples
            idx = rng.choice(n_samples, size=int(0.8 * n_samples), replace=False)
            km = KMeans(n_clusters=k, n_init=10, random_state=rng.integers(1e6))
            labels = km.fit_predict(data[idx])

            for i in range(len(idx)):
                for j in range(i + 1, len(idx)):
                    co_sampled[idx[i], idx[j]] += 1
                    co_sampled[idx[j], idx[i]] += 1
                    if labels[i] == labels[j]:
                        co_occurrence[idx[i], idx[j]] += 1
                        co_occurrence[idx[j], idx[i]] += 1

        
         np.errstate(divide=, invalid=):
            consensus = np.where(co_sampled > , co_occurrence / co_sampled, )

        
        km_final = KMeans(n_clusters=k, n_init=, random_state=seed)
        final_labels = km_final.fit_predict( - consensus)  
        sil = silhouette_score( - consensus, final_labels, metric=)

        results[k] = {: consensus, : sil, : final_labels}
        ()

     results



results = consensus_clustering(factors, k_range=(, ))


optimal_k = (results, key= k: results[k][])
()

R — ConsensusClusterPlus

library(ConsensusClusterPlus)
# input_mat: features x samples
results <- ConsensusClusterPlus(
  d = input_mat,
  maxK = 8,
  reps = 1000,
  pItem = 0.8,        # proportion of samples to subsample
  pFeature = 1,       # use all features
  clusterAlg = "km",  # k-means
  distance = "euclidean",
  seed = 42,
  plot = "pdf",
  title = "consensus_clustering"
)

# Inspect consensus CDF and delta area plots in output PDF
# Select k where CDF curve is flattest (highest consensus)

Consensus Clustering Parameter Table

Parameter	Python (custom)	R (ConsensusClusterPlus)
k range	k_range=range(2, 9)	maxK = 8
Iterations	n_iterations=100	reps = 1000
Subsample fraction	0.8 (hardcoded)	pItem = 0.8
Algorithm	KMeans	clusterAlg = "km"
Selection criterion	Silhouette score	CDF delta area plot

---

Common Mistakes

• Wrong: Mapping gene IDs using symbol-based joins without handling duplicates or deprecated symbols Right: Use HGNC ID or Ensembl stable ID as the primary key; resolve ambiguous symbols via the HGNC multi-symbol checker Why: Gene symbols are not unique (e.g., "MARCH1" was renamed to "MARCHF1") — symbol joins silently drop or duplicate rows

• Wrong: Running ComBat without including biological covariates in the model matrix Right: Always pass mod = model.matrix(~ disease_status + sex, data=meta) to protect biological signal Why: Without protected covariates, ComBat removes biological variation that correlates with batch

• Wrong: Using mofapy2 with raw counts instead of normalized, variance-stabilized data Right: Apply log2(CPM+1) or VST to RNA-seq counts before passing to MOFA; use log2 intensity for proteomics Why: MOFA assumes Gaussian-distributed continuous data — raw counts violate this and produce meaningless factors

• Wrong: Running gseapy/fgsea with a gene list ranked by fold change alone (no significance weighting) Right: Rank by -log10(p) × sign(log2FC) or use the Wald statistic from DESeq2/limma Why: Fold-change-only ranking treats noisy large-FC genes the same as significant ones, inflating false enrichments

• Wrong: Using default min_size=1 in fgsea, allowing tiny gene sets to appear significant Right: Set minSize=15, maxSize=500 to filter gene sets to biologically interpretable sizes Why: Very small gene sets produce unstable enrichment scores; very large sets are too generic to be informative