算法艺术创作
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consensus-clustering-analysis【设计与创意】Use when identifying stable sample subtypes from bulk expression matrices with ConsensusClusterPlus, including PAC-based model selection and consensus matrix/CDF visualization. NOT for: differential expression analysis, single-cell clustering workflows, or non-expression tables.
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Use this skill when you need to identify stable sample subtypes from a bulk expression matrix with ConsensusClusterPlus, compare candidate clustering settings with PAC, and export consensus matrix/CDF visualizations.
Do not use this skill for differential expression analysis, single-cell clustering, or non-expression tabular data.
| Situation | File to Read | Purpose |
|---|---|---|
| Need algorithm details | references/algorithm.md | Consensus clustering, PAC scoring, and preprocessing assumptions |
| Need to run analysis | scripts/main.R | Execute: Rscript scripts/main.R --input_file ... --group_file ... |
| Encounter errors | references/troubleshooting.md | Common errors and solutions |
| Need CLI examples | references/cli-guide.md | Detailed CLI usage examples with verified local runs |
Rscript scripts/main.R \
--input_file ./expression_matrix.csv \
--group_file ./groups.csv \
--disease_group case \
--max_k 4 \
--output_dir ./output/ \
--gene_selection highly_variable \
--top_n 5000 \
--reps 1000 \
--p_item 0.8 \
--p_feature 1.0 \
--timeout_seconds 3600 \
--seed 42
| Short | Long | Type | Default | Description |
|---|---|---|---|---|
-i | --input_file | character | required | Expression matrix file (genes as rows, samples as columns) |
-g | --group_file | character | required | Group information file (sample ID + group columns) |
-d | --disease_group | character | case | Group label retained for clustering |
-k | --max_k | integer | 4 | Maximum cluster count to evaluate |
-o | --output_dir | character | ./output/ | Output directory |
-m | --gene_selection | character | highly_variable | Gene selection mode: highly_variable or custom |
-n | --top_n | integer | 5000 | Number of top variable genes to keep |
-l | --gene_list | character | NULL | Custom gene list file when gene_selection=custom |
-c | --center_data | logical | TRUE | Median-center each gene before clustering |
-r | --reps | integer | 1000 | Consensus resampling repetitions |
--p_item | double | 0.8 | Sample resampling proportion | |
--p_feature | double | 1.0 | Feature resampling proportion | |
-t | --timeout_seconds | integer | 3600 | Elapsed timeout in seconds |
-s | --seed | integer | 42 | Random seed for reproducibility |
Genes as rows, samples as columns, CSV/TSV/TXT format with gene ID in the first column.
,Sample01,Sample02,Sample03
TSPAN6,1.8479,1.8318,3.8276
TNMD,0.0349,0.0533,1.3889
Delimited text file with sample ID and group columns.
sample,group
Sample01,case
Sample02,control
Sample03,case
Optional plain text or single-column CSV file with one gene symbol per line.
TNMD
DPM1
SCYL3
| File | Description |
|---|---|
Cluster_res.csv | PAC summary for each distance/algorithm combination with is_best marking the selected model |
genes_for_clustering.csv | Selected genes and gene selection mode |
samples_for_clustering.csv | Samples retained after disease-group filtering |
result_<distance>_<algorithm>/ | Method-specific consensus outputs and PAC_scores.csv |
Consensus Matrix Plot.pdf | Consensus matrix heatmap for the optimal model |
CDF curve Plot.pdf | CDF curves for the optimal method |
session_info.txt | R session and package version info |
highly_variable or customRepeated subsampling is used to estimate cluster stability across candidate K values and clustering settings.
The proportion of ambiguous clustering is computed as CDF(0.9) - CDF(0.1) from lower-triangle consensus values. Lower PAC indicates more stable clustering.
highly_variable: rank genes by median absolute deviationcustom: use the intersection of the provided gene list and matrix row namesRscript scripts/main.R \
-i expression_matrix.csv \
-g groups.csv \
-d case \
-k 3 \
-r 20 \
-o output/example_basic \
-t 120
Rscript scripts/main.R \
-i expression_matrix.csv \
-g groups.csv \
-d case \
-m custom \
-l genes.csv \
-k 4 \
-r 20 \
-o output/example_custom \
-t 120
Rscript scripts/main.R \
-i expression_matrix.csv \
-g groups.csv \
-d case \
-c FALSE \
-k 3 \
-r 20 \
-o output/example_rawscale \
-t 120
| Error | Cause | Solution |
|---|---|---|
SKILL_FILE_NOT_FOUND | Input file does not exist | Check file path and permissions |
SKILL_MISSING_COLUMNS | Group file lacks sample/group columns | Verify column names in the group file |
SKILL_SAMPLE_MISMATCH | Sample names do not match | Ensure group file sample IDs match matrix columns |
SKILL_INVALID_PARAMETER | CLI value is invalid | Check allowed options and numeric ranges |
SKILL_INVALID_DATA | Too few samples/genes remain after filtering | Lower max_k or review the input data |
SKILL_TIMEOUT | Run exceeded the configured timeout | Increase timeout_seconds or reduce reps |
SKILL_DEPENDENCY_MISSING | Required R package is not installed | Install missing packages before rerunning |
IF error persists, READ: references/troubleshooting.md
# Check help
Rscript scripts/main.R --help
# Run analysis
Rscript scripts/main.R \
-i tests/data/expression_matrix.csv \
-g tests/data/groups.csv \
-d case \
-k 3 \
-r 20 \
-o output/example_basic \
-t 120
# Inspect selected model
cat output/example_basic/Cluster_res.csv
# Check output plots exist
ls -la output/example_basic
optparseset.seed() for reproducibilityrequireNamespace() dependency checksdata.table::fread() input readingSKILL.mdSKILL_* codesscripts/ directoryreferences/ directoryLast updated: 2026-04-17 | Version: 1.0.0